Devices & Diagnostics > Device
Product Overview
This product is intended for use in the control of the Randox Total Antioxidant Status assay,
"TOTAL ANTIOXIDANT STATUS (TAS CONTROL)" - NX2331
This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry systems.
ABAXIS CHEMISTRY CONTROL LEVEL 1 - 1100-9131E
This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry
ABAXIS CHEMISTRY CONTROL LEVEL 2 - 1100-9132E
The paracetamol test system is intended for the quantitative in vitro determination of Acetaminophen in human serum.
ACE - ACE4023
ACID PHOSPHATASE (ACP)
ACID PHOSPHATASE (ACP) - AC8001
Acid Wash Solution should be used in conjunction with reagents to clean probes and cuvettes
ACID WASH SOLUTION (WASH SOLN. 3) - RX8129
The acid phosphatase test system is intended for the quantitative in vitro determination of Acid Phosphatase in serum.
ACP - AC1011
The Active Vitamin B12 Control Level 1 is intended for use with in vitro diagnostic assays for the quantitative determination of active Vitamin B12 (Holotranscobalamin/HoloTC) in human serum and plasma. The Active Vitamin B12 Control Level 1 is assayed with target values and are suitable for use on various analysers. The Active Vitamin B12 Control Level 1 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
ACTIVE VITAMIN B12 CONTROL LEVEL 1 - VB10524
The Active Vitamin B12 Control Level 2 is intended for use with in vitro diagnostic assays for the quantitative determination of active Vitamin B12 (Holotranscobalamin/HoloTC) in human serum and plasma. The Active Vitamin B12 Control Level 2 is assayed with target values and are suitable for use on various analysers. The Active Vitamin B12 Control Level 2 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
ACTIVE VITAMIN B12 CONTROL LEVEL 2 - VB10525
ADIPONECTIN CALIBRATOR (ADPN CAL)
ADIPONECTIN CALIBRATOR (ADPN CAL) - AO2800
ADIPONECTIN CONTROL - LEVEL 2 (ADPN CONTROL 2)
ADIPONECTIN CONTROL - LEVEL 2 (ADPN CONTROL 2) - AO2801
ADIPONECTIN CONTROL - LEVEL 3 (ADPN CONTROL 3)
ADIPONECTIN CONTROL - LEVEL 3 (ADPN CONTROL 3) - AO2802
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL100
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL1200
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL1205
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL1268
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL146
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL2360
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL7904
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL7930
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL8006
ALANINE AMINOTRANSFERASE (ALT)
ALANINE AMINOTRANSFERASE (ALT) - AL8304
An Albumin test system is a device intended for the quantitative in vitro determination of Albumin concentration in serum and plasma.
ALB - AB362
An Albumin test system is a device intended for the quantitative in vitro determination of Albumin concentration in serum and plasma.
ALB - AB3800
An Albumin test system is a device intended for the quantitative in vitro determination of Albumin concentration in serum.
ALB - AB8301
ALDOLASE (ALS)
ALDOLASE (ALS) - AD189
ALDOLASE LEVEL 2 CONTROL (ALS CONTROL 2)
ALDOLASE LEVEL 2 CONTROL (ALS CONTROL 2) - AD5001
ALDOLASE LEVEL 3 CONTROL (ALS CONTROL 3)
ALDOLASE LEVEL 3 CONTROL (ALS CONTROL 3) - AD5002
Alkaline Detergent is used for cleaning the instrument probe and reaction cuvettes.
ALKALINE DETERGENT (Alkaline Detergent) - RX8108
ALKALINE PHOSPHATASE (ALP)
ALKALINE PHOSPHATASE (ALP) - AP8302
Alkaline Wash Solution should be used in conjunction with reagents to clean cuvettes
ALKALINE WASH SOLUTION (WASH soln. 9) - RX8130
An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
ALP - AP311
An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
ALP - AP313
An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
ALP - AP3802
An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
ALP - AP3877
An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
ALP - AP7927
The ALP method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
ALP - AP2809
ALPHA-1-ACID-GLYCOPROTEIN (AGT)
ALPHA-1-ACID-GLYCOPROTEIN (AGT) - AG2472
The Aldolase Calibration Serum is intended for in vitro diagnostic use, in the calibration of the Aldolase assay AD189.
ALS CAL - AD5000
An ALT test system is a device intended for the quantitative in vitro determination of Alanine Aminotransferase (ALT) activity in serum and plasma.
ALT - AL3801
An ALT test system is a device intended for the quantitative in vitro determination of of Alanine Aminotransferase (ALT) activity in serum and plasma.
ALT - AL3875
The AMH Control Level 1 (AMH10509) is intended for use with in vitro diagnostic assays for the quantitative determination of Anti-Müllerian Hormone in human serum and plasma. The AMH Control Level 1 (AMH10509) is assayed with target values and is suitable for use on automated analysers.The AMH Control Level 1 (AMH10509) is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
AMH CONTROL LEVEL 1 (AMH CONTROL 1) - AMH10509
The AMH Control Level 2 (AMH10514) is intended for use with in vitro diagnostic assays for the quantitative determination of Anti-Müllerian Hormone in human serum and plasma. The AMH Control Level 2 (AMH10514) is assayed with target values and is suitable for use on automated analysers.The AMH Control Level 2 (AMH10514) is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
AMH CONTROL LEVEL 2 (AMH CONTROL 2) - AMH10514
The AMH Control Level 3 (AMH10515) is intended for use with in vitro diagnostic assays for the quantitative determination of Anti-Müllerian Hormone in human serum and plasma. The AMH Control Level 3 (AMH10515) is assayed with target values and is suitable for use on automated analysers.The AMH Control Level 3 (AMH10515) is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
AMH CONTROL LEVEL 3 (AMH CONTROL 3) - AMH10515
The AMH Control Level 4 (AMH10516) is intended for use with in vitro diagnostic assays for the quantitative determination of Anti-Müllerian Hormone in human serum and plasma. The AMH Control Level 4 (AMH10516) is assayed with target values and is suitable for use on automated analysers.The AMH Control Level 4 (AMH10516) is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
AMH CONTROL LEVEL 4 (AMH CONTROL 4) - AMH10516
AMMONIA (NH3)
AMMONIA (NH3) - AM1015
AMMONIA (NH3)
AMMONIA (NH3) - AM1054
The Randox Ammonia Ethanol Control Level 1 is intended for in vitro diagnostic use, in the quality control of Ammonia and Alcohol Assays to monitor precision and to detect systematic analytical deviations on clinical chemistry systems.
AMMONIA ETHANOL CONTROL - LEVEL 1 (NH3/EtOH CONTROL 1) - EA1366
The Randox Ammonia Ethanol Control - Level 2 is intended for in vitro diagnostic use, in the quality control of Ammonia and Alcohol Assays to monitor precision and to detect systematic analytical deviations on clinical chemistry systems.
AMMONIA ETHANOL CONTROL - LEVEL 2 (NH3/EtOH CONTROL 2) - EA1367
The Randox Ammonia Ethanol Control - Level 3 is intended for in vitro diagnostic use, in the quality control of Ammonia and Alcohol Assays to monitor precision and to detect systematic analytical deviations on clinical chemistry systems.
AMMONIA ETHANOL CONTROL - LEVEL 3 (NH3/EtOH CONTROL 3) - EA1368
An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, or urine.
AMY - AY7932
An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine.
AMY - AY3805
An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine.
AMY - AY7931
An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine.
AMY - AY9707
The AMY method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of amylase activity in serum, plasma and urine.
AMY - AY2811
The amylase test system is intended for the quantitative in vitro determination of Amylase in serum, plasma or urine.
AMY - AY1580
The amylase test system is intended for the quantitative in vitro determination of Amylase in serum, plasma or urine.
AMY - AY1582
Antibacterial Detergent is used for cleaning the instrument probe and reaction cuvettes.
ANTI-BACTERIAL DETERGENT (Detergent) - RX8106
Anti-Streptolysin O (ASO)
Anti-Streptolysin O (ASO) - LO2715
ANTI-STREPTOLYSIN O STANDARD (ASO STD)
ANTI-STREPTOLYSIN O STANDARD (ASO STD) - LO2306
ANTI-STREPTOLYSIN-O 2 (ASO 2)
ANTI-STREPTOLYSIN-O 2 (ASO 2) - LO3998
ANTI-STREPTOLYSIN-O 2 (ASO 2)
ANTI-STREPTOLYSIN-O 2 (ASO 2) - LO3999
ANTI-STREPTOLYSIN-O 2 (ASO 2)
ANTI-STREPTOLYSIN-O 2 (ASO 2) - LO8015
ANTI-STREPTOLYSIN-O 2 (ASO 2)
ANTI-STREPTOLYSIN-O 2 (ASO 2) - LO8305
Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma
APO A-I - LP2116
Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma
APO A-I - LP2866
Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma
APO A-I - LP2989
Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma
APO A-I - LP3838
An APO B test system is a device intended for the quantitative in vitro determination of Apolipoprotein B (APO B) in serum and plasma.
APO B - LP2117
An APO B test system is a device intended for the quantitative in vitro determination of Apolipoprotein B (APO B) in serum and plasma.
APO B - LP2990
An APO B test system is a device intended for the quantitative in vitro determination of Apolipoprotein B (APO B) in serum and plasma.
APO B - LP3839
Immunoturbidimetric assay for the quantitative in vitro determination of Apolipoprotein B in human serum.
APO B - LP2867
This product is intended for in-vitro use in the calibration of Apolipoprotein A-I and Apolipoprotein B assays.
APO CAL - LP3023
Apolipoprotein A1 & B Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Beckman Coulter AU Systems for Apolipoprotein A1 and Apolipoprotein B.
APOLIPOPROTEIN A1 & B LINEARITY VERIFIERS (For Beckman Coulter AU Systems) - LV10363
Apo Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for Apo A1 and Apo B.
APOLIPOPROTEIN A1 & B LINEARITY VERIFIERS (For Roche Systems) (ApoLV-R) - LV10357
APOLIPOPROTEIN A-I (APO A-I)
APOLIPOPROTEIN A-I (APO A-I) - LP8007
APOLIPOPROTEIN A-II (APO A-II)
APOLIPOPROTEIN A-II (APO A-II) - LP3867
APOLIPOPROTEIN B (APO B)
APOLIPOPROTEIN B (APO B) - LP8008
APOLIPOPROTEIN CALIBRATOR 2 (APO CAL 2)
APOLIPOPROTEIN CALIBRATOR 2 (APO CAL 2) - LP5047
APOLIPOPROTEIN C-II (APO C-II)
APOLIPOPROTEIN C-II (APO C-II) - LP3866
APOLIPOPROTEIN C-III (APO C-III)
APOLIPOPROTEIN C-III (APO C-III) - LP3865
APOLIPOPROTEIN CONTROL - LEVEL 1 (APO CONTROL 1)
APOLIPOPROTEIN CONTROL - LEVEL 1 (APO CONTROL 1) - LE5016
APOLIPOPROTEIN CONTROL - LEVEL 2 (APO CONTROL 2)
APOLIPOPROTEIN CONTROL - LEVEL 2 (APO CONTROL 2) - LE5017
APOLIPOPROTEIN CONTROL - LEVEL 3 (APO CONTROL 3)
APOLIPOPROTEIN CONTROL - LEVEL 3 (APO CONTROL 3) - LE5018
APOLIPOPROTEIN E (APO E)
APOLIPOPROTEIN E (APO E) - LP3864
ASPARTATE AMINOTRANSFERASE (AST)
ASPARTATE AMINOTRANSFERASE (AST) - AS101
ASPARTATE AMINOTRANSFERASE (AST)
ASPARTATE AMINOTRANSFERASE (AST) - AS147
ASPARTATE AMINOTRANSFERASE (AST)
ASPARTATE AMINOTRANSFERASE (AST) - AS8005
ASSAYED BOVINE MULTI SERA - LEVEL 1 (BOV ASY CONTROL 1)
ASSAYED BOVINE MULTI SERA - LEVEL 1 (BOV ASY CONTROL 1) - AL1027
ASSAYED BOVINE MULTI SERA - LEVEL 2 (BOV ASY CONTROL 2)
ASSAYED BOVINE MULTI SERA - LEVEL 2 (BOV ASY CONTROL 2) - AN1026
ASSAYED BOVINE MULTI SERA - LEVEL 3 (BOV ASY CONTROL 3)
ASSAYED BOVINE MULTI SERA - LEVEL 3 (BOV ASY CONTROL 3) - AE1032
ASSAYED URINE CONTROL - LEVEL 2 (URN ASY CONTROL 2)
ASSAYED URINE CONTROL - LEVEL 2 (URN ASY CONTROL 2) - AU2352
ASSAYED URINE CONTROL - LEVEL 3 (URN ASY CONTROL 3)
ASSAYED URINE CONTROL - LEVEL 3 (URN ASY CONTROL 3) - AU2353
The AST method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of aspartate aminotransferase activity in serum or plasma.
AST - AS2800
The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AST - AS1202
The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AST - AS1204
The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AST - AS1267
The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AST - AS2359
The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AST - AS3804
The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AST - AS3876
The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AST - AS7905
The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AST - AS7938
The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AST - AS8306
This product should be used in conjunction with RX daytona plus reagents to clean probes and cuvettes.
AWS - WS8397
This product should be used in conjunction with RX SERIES reagents to clean probes and cuvettes.
AWS - WS3853
B2Microglobulin (B2M)
B2Microglobulin (B2M) - BM3887
B2Microglobulin (B2M)
B2Microglobulin (B2M) - BM8016
The Barbiturates assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of Barbiturates in human urine.
BARB - DA4008
The Benzodiazepine assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of Benzodiazepines in human urine
BENZ - DA4009
The Randox Benzodiazepines Calibrator Set is intended for use in the calibration of the Benzodiazepines assay. The Calibrator Set contains 5 levels of calibrator containing the specific drug Oxazepam.
BENZ CAL - DA3129
The Randox Benzodiazepines Control Level 1 is intended for use in the Quality Control of the Benzodiazepines (BENZ) assay. The Benzodiazepine Control Level 1 contains the specific drug Oxazepam.
BENZ CONTROL 1 - DA3130
The Randox Benzodiazepines Control Level 2 is intended for use in the Quality Control of the Benzodiazepines (BENZ) assay. The Benzodiazepine Control Level 2 contains the specific drug Oxazepam.
BENZ CONTROL 2 - DA3131
BETA 2 MICROGLOBULIN CALIBRATOR (B2M CAL)
BETA 2 MICROGLOBULIN CALIBRATOR (B2M CAL) - BM1362
The device is intended for the quantitative in vitro determination of total and direct bilirubin in serum or plasma.
BIL - BR411
The device is intended for the quantitative in vitro determination of total and direct bilirubin in serum or plasma.
BIL - BR412
BILIRUBIN ELEVATED SERUM (BIL CONTROL H)
BILIRUBIN ELEVATED SERUM (BIL CONTROL H) - BE454
Bilirubin Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for Total and Direct Bilirubin.
BILIRUBIN LINEARITY VERIFIER (For Roche Systems) (BILIRUBIN LIN VER ROCHE) - LV10356
BLOOD GAS CONTROL - LEVEL 1 (BG CONTROL 1)
BLOOD GAS CONTROL - LEVEL 1 (BG CONTROL 1) - BG5001
BLOOD GAS CONTROL - LEVEL 2 (BG CONTROL 2)
BLOOD GAS CONTROL - LEVEL 2 (BG CONTROL 2) - BG5002
BLOOD GAS CONTROL - LEVEL 3 (BG CONTROL 3)
BLOOD GAS CONTROL - LEVEL 3 (BG CONTROL 3) - BG5003
The BNP Controls for Abbott (CQ10521) are intended for use with in vitro diagnostic assays for the quantitative determination of BNP in human serum and plasma. The BNP Controls for Abbott (CQ10521) are assayed with target values and are suitable for use on Abbott analysers. The BNP Controls for Abbott (CQ10521) are for use by trainedlaboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
BNP CONTROLS FOR ABBOTT (BNP CONTROL) - CQ10521
The BNP Controls for Beckman (CQ10520) are intended for use with in vitro diagnostic assays for the quantitative determination of BNP in human serum and plasma. The BNP Controls for Beckman (CQ10520) are assayed with target values and are suitable for use on Beckman analysers. The BNP Controls for Beckman (CQ10520) are for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
BNP CONTROLS FOR BECKMAN (BNP CONTROL) - CQ10520
BOVINE PRECISION MULTI SERA - LEVEL 1 (BOV PREC CONTROL 1)
BOVINE PRECISION MULTI SERA - LEVEL 1 (BOV PREC CONTROL 1) - SL1084
BOVINE PRECISION MULTI SERA - LEVEL 2 (BOV PREC CONTROL 2)
BOVINE PRECISION MULTI SERA - LEVEL 2 (BOV PREC CONTROL 2) - SN1085
BOVINE PRECISION MULTI SERA - LEVEL 3 (BOV PREC CONTROL 3)
BOVINE PRECISION MULTI SERA - LEVEL 3 (BOV PREC CONTROL 3) - SE1086
Diluted wash buffer is used for washing the biochips between assay steps to remove all unbound materials.
BUF WASH (conc.) - EV3581
The BUN method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of urea nitrogen in serum, plasma and urine.
BUN - UR2821
BUTYRYL CHOLINESTERASE (CHE)
BUTYRYL CHOLINESTERASE (CHE) - CE190
BUTYRYL CHOLINESTERASE (CHE)
BUTYRYL CHOLINESTERASE (CHE) - CE7944
The Cocaine assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of benzoylecgonine (Cocaine Metabolite) in human urine.
BZG - DA4011
This product is a weak bleach solution.
C1 SOLUTION (C1 SOLN) - RX8143
A Complement C3 test system is a device intended for the quantitative in vitro determination of Complement C3 concentration in serum
C3 - CM3845
A Complement C4 test system is a device intended for the quantitative in vitro determination of Complement C4 concentration in serum
C4 - CM3846
The calcium method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of calcium concentration in serum.
Ca - CA2807
The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine
Ca - CA3871
The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine
Ca - CA7941
The calcium test system is a device intended for the quantitative in vitro determination of calcium in serum, plasma or urine
Ca - CA590
The device is intended for use as a calibrator in clinical chemistry assays. Randox calibration sera are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry assays on a wide range of automatic analyzers.
CAL 2 - CAL2350
The device is intended for use as a calibrator in clinical chemistry assays. Randox calibration sera are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry assays on a wide range of automatic analyzers.
CAL 3 - CAL2351
The product is intended to be used as a wash solution and single point calibrator. Calibrator A is pumped into the sample port by the Calibrator A pump and then positioned in front of the sensor.
CAL A - RX4000
The product is intended to be used as a second Calibrator in a two-point calibration. Calibrator B is aspirated from a sample cup at position 18 on the analyser ASP tray at least once every 8 hours depending on the laboratories schedule.
CAL B - RX3949
CALCIUM (Ca)
CALCIUM (Ca) - CA8309
The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine
Calcium (Ca) - CA2390
This product is intended for in vitro use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems.
CARDIAC CONTROL - LEVEL 1 (CRD CONTROL 1) - CQ10429
This product is intended for in vitro use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems.
CARDIAC CONTROL - LEVEL 2 (CRD CONTROL 2) - CQ10430
This product is intended for in vitro use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems.
CARDIAC CONTROL - LEVEL 3 (CRD CONTROL 3) - CQ10431
This product is intended for intended for use with in vitro diagnostic assays, for the quantitative determination of Troponin I. Cardiac Controls are unassayed without target values and are suitable for use on automated analysers. Cardiac Controls are for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
CARDIAC ULTRA LOW CONTROL (CRD CONTROL Ultra Low) - CQ10428
For the quantitative in vitro determination of Carbamazepine in human serum
CBZ - TD3416
CERULOPLASMIN (CPL)
CERULOPLASMIN (CPL) - CPL4017
CHEMISTRY PREMIUM - LEVEL 2 (CHEM PREMIUM 2)
CHEMISTRY PREMIUM - LEVEL 2 (CHEM PREMIUM 2) - HN5067
CHEMISTRY PREMIUM - LEVEL 3 (CHEM PREMIUM 3)
CHEMISTRY PREMIUM - LEVEL 3 (CHEM PREMIUM 3) - HE5068
For the quantitative in vitro determination of cholesterol in serum and plasma.
CHOL - CH3810
CHOLESTEROL (CHOL)
CHOLESTEROL (CHOL) - CH8019
For the quantitative in vitro determination of Cholesterol in serum and plasma.
CHOLESTEROL (CHOL) - CH200
For the quantitative in vitro determination of cholesterol in serum and plasma.
CHOLESTEROL (CHOL) - CH8310
The CK method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of creatine kinase activity in serum or plasma.
CK - CK2813
The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.
CK NAC - CK110
The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.
CK NAC - CK113
The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.
CK NAC - CK335
The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.
CK NAC - CK3812
The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.
CK NAC - CK3878
The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.
CK NAC - CK522
The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma.
CK-MB - CK1296
The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma.
CK-MB - CK1553
The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma.
CK-MB - CK4043
The device is intended for use in the calibration of CK-MB assays in clinical chemistry systems.
CK-MB CAL - CK2393
The device is intended for use in the quality control of CK-MB assays on clinical chemistry systems.
CK-MB CONTROL - CK1212
The device is intended for the quantitative in vitro determination of creatine kinase activity in serum or plasma.
CK-NAC - CK7947
Cleaning Solution for the RX series analysers
Cl SOLN - RX3973
Clinical Chemistry Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of the Roche Systems for Albumin, BUN, Calcium, Total Cholesterol, Creatinine, Glucose, Lactate, Lithium, Magnesium, Phosphate, Total Protein, Triglycerides, Uric acid, Iron, Sodium, Potassium and Chloride assays.
CLINICAL CHEMISTRY LINEARITY VERIFIERS (For Roche Systems) - LV10390
The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
CO2 - CD116
The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
CO2 - CD127
The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
CO2 - CD129
The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
CO2 - CD7942
CO2/Electrolyte Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of the Roche Systems for Carbon Dioxide, Sodium, Potassium, and Chloride.
CO2/ELECTROLYTE LINEARITY VERIFIERS (For Roche Systems) (CO2 LIN VER) - LV10362
COAGULATION CALIBRATOR (COAG CAL)
COAGULATION CALIBRATOR (COAG CAL) - CG5037
COAGULATION CONTROL - LEVEL 1 (COAG CONTROL 1)
COAGULATION CONTROL - LEVEL 1 (COAG CONTROL 1) - CG5021
COAGULATION CONTROL - LEVEL 2 (COAG CONTROL 2)
COAGULATION CONTROL - LEVEL 2 (COAG CONTROL 2) - CG5022
COAGULATION CONTROL - LEVEL 3 (COAG CONTROL 3)
COAGULATION CONTROL - LEVEL 3 (COAG CONTROL 3) - CG5023
The Randox ConcizuTrace™ sample collection kit is used for the collection and transportation of blood samples, taken by a trained phlebotomist. The samples will be transported to a professional laboratory for testing using either the ConcizuTrace™ ELISA kit or Concizumab ELISA kit.
ConcizuTrace™ Sample Collection Kit - CZM10596
COPPER (Cu)
COPPER (Cu) - CU2340
The CREA method used on the Dimension clinical chemistry system is an in vitro diagnostic device intended for the quantitative determination of Creatinine in serum, plasma or urine
CREA - CR2804
The device intended for the quantitative in vitro determination of Creatinine in serum, plasma or urine
CREA - CR524
The is intended for the quantitative in vitro diagnostic determination of Creatinine in serum, plasma or urine
CREA - CR3814
The is intended for the quantitative in vitro diagnostic determination of Creatinine in serum, plasma or urine
CREA - CR7948
The is intended for the quantitative in vitro diagnostic determination of Creatinine in serum, plasma or urine
CREA - CR8316
C-Reactive Protein Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for C-reactive protein (CRP).
C-REACTIVE PROTEIN LINEARITY VERIFIERS (For Roche Series) (CPLV) - LV10334
CREATININE (CREA)
CREATININE (CREA) - CR510
The CRP test system is intended for the quantitative in vitro determination of CRP concentration in serum.
CRP - CP3826
The CRP test system is intended for the quantitative in vitro determination of CRP concentration in serum.
CRP - CP7950
The CRP test system is intended for the quantitative in vitro determination of CRP concentration in serum.
CRP - CP9742
The device is a latex agglutination slide test intended for qualitative and semi-quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum.
CRP - CP1423
The device is a latex agglutination slide test intended for qualitative and semi-quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum.
CRP - CP2714
The device is intended for the quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum.
CRP - CP2572
The device is intended for the quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum.
CRP - CP7949
The XCRP method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of CRP in serum.
CRP - CP2852
The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems.
CRP CAL - CP2179
The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems.
CRP CAL - CP2479
The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems.
CRP CAL - CP2499
This product is intended for in vitro diagnostic use, in the quality control of diagnostic methods using CSF as a sample on clinical chemistry systems. The CSF controls are for the control of accuracy.
CSF CONTROL - LEVEL 2 (CSF CONTROL 2) - CF1500
This product is intended for in vitro diagnostic use, in the quality control of diagnostic methods using CSF as a sample on clinical chemistry systems. The CSF controls are for the control of accuracy.
CSF CONTROL - LEVEL 3 (CSF CONTROL 3) - CF1501
The device is intended for the quantitative in vitro determination of Cystatin C in serum or plasma.
CYSC - CYS4004
The device is intended to be used for in the calibration of Cystatin C assays.
CYSC CAL - CYS2699
Intended for in vitro diagnostic (IVD) use in the calibration of Randox Cystatin C assay. For use in a clinical laboratory setting by trained personnel.
CYSTATIN C CALIBRATOR (CYSC CAL) - CYS10445
Intended for in vitro diagnostic (IVD) use in quality control of Randox Cystatin C assay. For use in a clinical laboratory setting by trained personnel.
CYSTATIN C CONTROL - LEVEL 2 (CYSC CONTROL 2) - CYS10446
The Cystatin C Control is intended for use with in vitro diagnostic assays for the quantitative determination of Cystatin C. Cystatin C Control is assayed with target values and it is suitable for use on automated analysers.
CYSTATIN C CONTROL - LEVEL 2 (CYSC CONTROL 2) - CYS5019
Intended for in vitro diagnostic (IVD) use in quality control of Randox Cystatin C assay. For use in a clinical laboratory setting by trained personnel.
CYSTATIN C CONTROL - LEVEL 3 (CYSC CONTROL 3) - CYS10447
The Cystatin C Control is intended for use with in vitro diagnostic assays for the quantitative determination of Cystatin C. Cystatin C Control is assayed with target values, and it is suitable for use on automated analysers.
CYSTATIN C CONTROL - LEVEL 3 (CYSC CONTROL 3) - CYS5020
"Randox Cytokine controls are intended for use as an assayed quality control in the routine monitoring of accuracy and precision for the analytes listed in this insert.The Randox Cytokine Controls are multi-analyte. Each control contains all of the analytes listed overleaf. There are 3 levels of control: low, medium and high; Level 1, 2 and 3 respectively. "
CYTOKINE CONTROLS (CTK CONTROL) - CY5006
Randox Cytokine high sensitivity controls are intended for use as an assayed quality control in the routine monitoring of accuracy and precision for the analytes listed in this insert. The Randox Cytokine high sensitivity controls are multi-analyte. Each control contains all of the analytes listed overleaf. There are 3 levels of control: low, medium and high; Level 1, 2 and 3 respectively.
CYTOKINE HIGH SENSITIVITY CONTROLS (CTK HS CONTROL) - CY5005
The DBIL method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of direct (conjugated) bilirubin in serum or plasma.
D BIL - BR2801
The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma.
D BIL - BR2362
The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma.
D BIL - BR3807
The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma.
D BIL - BR8308
The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma.
D BIL - BR9765
The device is intended for in vitro diagnostic use in the calibration of Randox HDL and LDL cholesterol clearance methods
D LDL/HDL CAL - CH2673
D-3 Hydroxybutyrate (RANBUT)
D-3 Hydroxybutyrate (RANBUT) - RB1007
D-3 Hydroxybutyrate (RANBUT)
D-3 Hydroxybutyrate (RANBUT) - RB1008
For the quantitative in vitro determination of Digoxin in human serum
DG - TD3410
The Direct Bilirubin test system is a device intended for the quantitative in vitro determination of Direct Bilirubin in serum and plasma.
DIRECT BILIRUBIN 2 (D BIL 2) - BR8376
DIRECT HDL-CHOLESTEROL (HDL)
DIRECT HDL-CHOLESTEROL (HDL) - CH8033
Enzymatic Clearance assay for the in vitro quantitative determination of HDL-cholesterol in human serum and plasma.
DIRECT HDL-CHOLESTEROL (HDL) - CH1383
Enzymatic Clearance assay for the in vitro quantitative determination of HDL-cholesterol in human serum and plasma.
DIRECT HDL-CHOLESTEROL (HDL) - CH2655
For the quantitative in vitro determination of HDL Cholesterol in serum and plasma.
DIRECT HDL-CHOLESTEROL (HDL) - CH8311
DIRECT LDL-CHOLESTEROL (LDL)
DIRECT LDL-CHOLESTEROL (LDL) - CH8032
DIRECT LDL-CHOLESTEROL (LDL)
DIRECT LDL-CHOLESTEROL (LDL) - CH8312
Enzymatic Clearance assay for the in vitro quantitative determination of LDL-cholesterol in human serum and plasma.
DIRECT LDL-CHOLESTEROL (LDL) - CH2656
Diluted displacement fluid is used to wash the Evidence™ reagent tubing between dispenses.
DISP FL (conc.) - EV3580
The Evidence® Drugs of Abuse (DOA) Assays are in-vitro diagnostic tests for the qualitative determination of the parent molecule and metabolites of drugs in human urine. They are competitive enzyme immunoassays.
DOA - EV3500
The Evidence® Drugs of Abuse (DOA) Assays are in-vitro diagnostic tests for the qualitative determination of the parent molecule and metabolites of drugs in human urine. They are competitive enzyme immunoassays.
DOA - EV3542
Evidence® Drugs of Abuse Calibrators are intended for in vitro diagnostic use in the calibration of the Randox Drugs of Abuse Panel on the Evidence® analyser.
DOA CAL - EV3550
The Randox Multidrug Calibrator Set is intended for use in the calibration of Methamphetamine, Barbiturates, Cocaine Metabolite, Methadone and Opiate assays.
DOA CAL - DA2704
The Randox Multidrug Control Level 1 is intended for use in the Quality Control of Methamphetamine, Barbiturates, Cocaine, Methadone and Opiates assays.
DOA CONTROL 1 - DA3121
The Randox Multidrug Control Level 2 is intended for use in the Quality Control of Methamphetamine, Barbiturates, Cocaine, Methadone and Opiates assays.
DOA CONTROL 2 - DA3122
This product is intended for in vitro diagnostic use in the quality control of drug residue analysis on clinical chemistry systems. TheDrug Controls are for the control of accuracy and precision.
DRUG CONTROL - LEVEL 1 (TDM CONTROL 1) - HD1667
This product is intended for in vitro diagnostic use in the quality control of drug residue analysis on clinical chemistry systems. The Drug Controls are for the control of accuracy and precision.
DRUG CONTROL - LEVEL 2 (TDM CONTROL 2) - HD1668
This product is intended for in vitro diagnostic use in the quality control of drug residue analysis on clinical chemistry systems. The Drug Controls are for the control of accuracy and precision.
DRUG CONTROL - LEVEL 3 (TDM CONTROL 3) - HD1669
The EDDP assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) in human urine.
EDDP - DA4013
The Randox EDDP Calibrator Set is intended for use in the calibration of the 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) assay.
EDDP CAL - DA2702
The Randox EDDP Control - Level 1 is intended for use in the Quality Control of the 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) assay. The EDDP Control - Level 1 contains the specific drug EDDP.
EDDP CONTROL 1 - DA3123
The Randox EDDP Control - Level 2 is intended for use in the Quality Control of the 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) assay. The EDDP Control - Level 2 contains the specific drug EDDP.
EDDP CONTROL 2 - DA3124
Enzymes Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for ALT, AST, Alkaline Phosphatase (ALP), Total Amylase, Pancreatic Amylase, CK, CKMB, Gamma GT, LDH and Lipase assays.
ENZYMES LINEARITY VERIFIER (For Roche Systems) (ENZYMES LIN VER ROCHE) - LV10366
Esoteric Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of the Roche Systems for Acetaminophen, Ammonia, Ethanol, Salicylate, Microalbumin and Urinary Protein assays.
ESOTERIC LINEARITY VERIFIERS (For Roche Systems) (ESOTERIC LIN VER ROCHE) - LV10336
The Blood Sample Collection Kit is intended for use in the collection and transport of a blood sample, taken by a trained phlebotomist. The samples will be transported to a professional laboratory for testing.
ESSENTIAL PACKAGE SAMPLE COLLECTION KIT (USA) - SCK10684
This should be run on a weekly basis to prevent protein build up.
ETCH - RX4048
The ethanol assay is an in vitro diagnostic test for the quantitative analysis of ethanol in human urine and serum.
EtOH - DA4015
The Randox Ethanol Calibrator and Control Set is intended for the calibration and quality control of the Randox Ethanol assay, which is used for the quantitative analysis of ethanol in human urine and serum.
EtOH CAL/CONTROL - DA2703
The Blood Sample Collection Kit is intended for use in the collection and transport of a blood sample, taken by a trained phlebotomist. The samples will be transported to a professional laboratory for testing.
EXTENDED PACKAGE SAMPLE COLLECTION KIT (USA U60) - SCK10689
The Blood Sample Collection Kit is intended for use in the collection and transport of a blood sample, taken by a trained phlebotomist. The samples will be transported to a professional laboratory for testing.
EXTENDED PACKAGE SAMPLE COLLECTION KIT (USA) - SCK10685
The product is an in vitro diagnostic test intended for the quantitative determination of Iron in serum
Fe - SI2818
The product is intended for the quantitative in vitro determination of Iron in serum and plasma
Fe - SI3821
The product is intended for the quantitative in vitro determination of Iron in serum and plasma
Fe - SI7967
This product is intended for the quantitative in vitro determination of Iron in serum.
Fe - SI257
This product is intended for the quantitative in vitro determination of Ferritin in serum or plasma.
FERR - FN3452
This product is intended for the quantitative in vitro determination of Ferritin in serum or plasma.
FERR - FN3453
This product is intended for the quantitative in vitro determination of Ferritin in serum or plasma.
FERR - FN3888
The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma.
frCRP - CP3847
The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma.
frCRP - CP3849
The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma.
frCRP - CP3850
Enzymatic assay for the quantitative in vitro determination of glycated protein (fructosamine) in human serum or plasma.
FRUC - FR3133
This product is intended for in vitro diagnostic use in the calibration of the Randox Liquid Fructosamine assay on clinical chemistry systems.
FRUC CAL - FR2993
This product is intended for in vitro diagnostic use in the quality control of the Randox Liquid Fructosamine assay on clinical chemistry systems.
FRUC CONTROL 1 - FR2994
This product is intended for in vitro diagnostic use in the quality control of the Randox Liquid Fructosamine assay on clinical chemistry systems.
FRUC CONTROL 3 - FR2996
FRUCTOSAMINE (FRUC)
FRUCTOSAMINE (FRUC) - FR4030
G-6-PDH DEFICIENT CONTROL (G-6-PDH CONTROL D)
G-6-PDH DEFICIENT CONTROL (G-6-PDH CONTROL D) - PD2617
G-6-PDH NORMAL CONTROL (G-6-PDH CONTROL N)
G-6-PDH NORMAL CONTROL (G-6-PDH CONTROL N) - PD2618
A Gamma GT test system is a device intended for the quantitative in vitro determination of L Gamma Glutamyltransferase (GGT) activity in serum and plasma.
GAMMA-GLUTAMYLTRANSERASE (GGT) - GT3874
A Gamma GT test system is a device intended for the quantitative in vitro determination of L Gamma Glutamyltransferase (GGT) activity in serum and plasma.
GAMMA-GLUTAMYLTRANSERASE (GGT) - GT8146
A Gamma GT test system is a device intended for the quantitative in vitro determination of L Gamma Glutamyltransferase (GGT) activity in serum.
GAMMA-GLUTAMYLTRANSERASE (GGT) - GT8320
For the quantitative in vitro determination of Gentamicin in human serum
GENT - TD3413
A GGT test system is a device intended for the quantitative in vitro determination of L Gamma Glutamyltransferase (GGT) activity in serum and plasma. This product is suitable for use on RX series instruments which includes the RX daytona and the RX imola.
GGT - GT3817
A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, lithium plasma and urine
GLUC-HK - GL3816
A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, lithium plasma and urine
GLUC-HK - GL3881
A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, plasma and urine
GLUC-HK - GL1611
A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, plasma and urine
GLUC-HK - GL2822
The product is intended for the quantitative in vitro determination of Glucose in serum or urine.
GLUC-HK - GL8319
The product is intended for the quantitative in vitro determination of Glucose in serum, plasma or urine.
GLUC-HK - GL7954
A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine
GLUC-PAP - GL1021
A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine
GLUC-PAP - GL2614
A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine
GLUC-PAP - GL2623
A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine
GLUC-PAP - GL364
A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine
GLUC-PAP - GL366
A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine
GLUC-PAP - GL3815
A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine
GLUC-PAP - GL3981
The product is intended for the quantitative in vitro determination of Glucose in serum, plasma or urine.
GLUC-PAP - GL7952
GLUTATHIONE REDUCTASE (GLUT RED)
GLUTATHIONE REDUCTASE (GLUT RED) - GR2368
GLUTATHIONE REDUCTASE CALIBRATION SERUM (GLUT RED CAL)
GLUTATHIONE REDUCTASE CALIBRATION SERUM (GLUT RED CAL) - GR2609
GLUTATHIONE REDUCTASE CONTROL SERUM (GLUT RED CONTROL)
GLUTATHIONE REDUCTASE CONTROL SERUM (GLUT RED CONTROL) - GR2608
GLYCEROL (GLY)
GLYCEROL (GLY) - GY105
GLYCEROL CONTROL (GLY CONTROL)
GLYCEROL CONTROL (GLY CONTROL) - GY1369
Used as a Calibrator in a two-point calibration. H Solution is aspirated from a sample cup located in a pre-registered position on the sample carousel.
H SOLN - RX4046
This product is intended for in vitro diagnostic use in the quality control of multiple haematology parameters
HAEM CNTL - LEVEL 1, 2, 3 - HM5162
HAEMATOLOGY CONTROL - LEVEL 1 (HAEM CNTL - LEVEL 1)
HAEMATOLOGY CONTROL - LEVEL 1 (HAEM CNTL - LEVEL 1) - HM10190
HAEMATOLOGY CONTROL - LEVEL 2 (HAEM CNTL - LEVEL 2)
HAEMATOLOGY CONTROL - LEVEL 2 (HAEM CNTL - LEVEL 2) - HM10191
HAEMATOLOGY CONTROL - LEVEL 3 (HAEM CNTL - LEVEL 3)
HAEMATOLOGY CONTROL - LEVEL 3 (HAEM CNTL - LEVEL 3) - HM10192
HAEMOGLOBIN A1c (HbA1c)
HAEMOGLOBIN A1c (HbA1c) - HA3450
HAEMOGLOBIN F AND A2 CONTROLS - LEVEL 1 AND 2 (Hb F & A2 CONTROL)
HAEMOGLOBIN F AND A2 CONTROLS - LEVEL 1 AND 2 (Hb F & A2 CONTROL) - HA5083
HAPTOGLOBIN (HP)
HAPTOGLOBIN (HP) - HP3886
A Haemoglobin A1c test system is a device intended for the quantitative in vitro determination of Haemoglobin A1c concentration in whole blood
HbA1C - HA3830
The product is intended for the quantitative in vitro determination of Haemoglobin A1c concentration in whole blood.
HbA1C - HA8321
This product is intended for in vitro diagnostic use in the calibration of HbA1c on clinical chemistry systems.
HbA1C CAL - HA3444
This product is intended for in vitro diagnostic use in the quality control of HbA1c on clinical chemistry systems.
HbA1C CONTROL - HA5072
The HbA1c II Calibrator is intended for use in the calibration of the HbA1c II assay.
HbA1c II CALIBRATOR SET (HbA1c II CAL) - HA8124
A homocysteine test system is a device intended for the quantitative in vitro determination of homocysteine concentration in human serum.
HCY - HY4036
An HDL-cholesterol test system is a device intended for the quantitative in vitro determination of HDL-cholesterol concentration in human serum and plasma.
HDL - CH3811
HDL-CHOLESTEROL (HDL)
HDL-CHOLESTEROL (HDL) - CH203
High Sensitivity C-Reactive Protein Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche systems for High Sensitivity C-reactive protein (hsCRP).
HIGH SENSITIVITY C-REACTIVE PROTEIN LINEARITY VERIFIERS (For Roche Series) - LV10335
Randox High Sensitivity CRP Control Level I is a ready to use control in a stabilised protein base. It is intended for use with the Randox High Sensitivity CRP Assay (Catalogue No. CP3885) for the control of accuracy and the control of reproducibility.
HIGH SENSITIVITY CRP CONTROL - LEVEL I (hsCRP CONTROL 1) - CP2476
Randox High Sensitivity CRP Control Level II is a ready to use control in a stabilised protein base. It is intended for use with the Randox High Sensitivity CRP Assay (Catalogue No. CP3885) for the control of accuracy and the control of reproducibility.
HIGH SENSITIVITY CRP CONTROL - LEVEL II (hsCRP CONTROL 2) - CP2477
The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma.
hsCRP - CP3885
The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems.
hsCRP CAL - CP2478
The Human Assayed Multi-sera is supplied at 2 levels, level 2 and 3. Target values and ranges are supplied for the analytes listed in the values section at both levels.
HUMAN ASSAYED MULTI-SERA/ASSAYED CHEMISTRY PREMIUM PLUS - LEVEL 2 & 3 (HUM ASY - HS2611
The Human Assayed Multi-sera is supplied at 2 levels, level 2 and 3. Target values and ranges are supplied for the analytes listed in the values section at both levels.
HUMAN ASSAYED MULTI-SERA/ASSAYED CHEMISTRY PREMIUM PLUS - LEVEL 2 (HUM ASY CONTR - HN1530
The Human Assayed Multi-sera is supplied at 2 levels, level 2 and 3. Target values and ranges are supplied for the analytes listed in the values section at both levels.
HUMAN ASSAYED MULTI-SERA/ASSAYED CHEMISTRY PREMIUM PLUS - LEVEL 3 (HUM ASY CONTR - HE1532
HUMAN PRECISION CONTROL - LEVEL 2 (HUM PREC CONTROL 2)
HUMAN PRECISION CONTROL - LEVEL 2 (HUM PREC CONTROL 2) - UN1557
HUMAN PRECISION CONTROL - LEVEL 3 (HUM PREC CONTROL 3)
HUMAN PRECISION CONTROL - LEVEL 3 (HUM PREC CONTROL 3) - UE1558
Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.
I.S.E. CL - D200-0016
Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.
I.S.E. CL - D400-0013
The product should be run on a weekly basis to prevent protein build up.
I.S.E. CLN - RX4047
Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.
I.S.E. K - D200-0015
Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.
I.S.E. K - D400-0012
Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.
I.S.E. NA - D200-0014
Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.
I.S.E. NA - D400-0011
Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.
I.S.E. REF - D200-0017
Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine.
I.S.E. REF - D400-0010
The product is intended for the quantitative in vitro determination of IgA in serum or plasma.
IgA - IA2447
The product is intended for the quantitative in vitro determination of IgA in serum or plasma.
IgA - IA3832
The product is intended for the quantitative in vitro determination of IgA in serum or plasma.
IgA - IA3895
The product is intended for the quantitative in vitro determination of IgA in serum or plasma.
IgA - IA7157
An IgE test system is a device intended for the quantitative in vitro determination of immunoglobulin E (IgE) concentration in human serum or plasma
IgE - IE7308
This product is intended for in vitro diagnostic use in the quality control of IgE on clinical chemistry systems.
IgE CAL SET - IE2492
IgG
IgG - IG3896
The IgG test system is a device intended for the quantitative in vitro determination of immunoglobulin G (IgG) concentration in serum and plasma
IgG - IG2448
The IgG test system is a device intended for the quantitative in vitro determination of immunoglobulin G (IgG) concentration in serum and plasma
IgG - IG3833
The IgG test system is a device intended for the quantitative in vitro determination of immunoglobulin G (IgG) concentration in serum and plasma
IgG - IG7158
For the quantitative in vitro determination of IgM in serum and plasma
IgM - IM3834
For the quantitative in vitro determination of IgM in serum and plasma
IgM - IM7977
This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.
IMMUNOASSAY PREMIUM - LEVEL 1 (IA PREMIUM 1) - IA2638
This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.
IMMUNOASSAY PREMIUM - LEVEL 2 (IA PREMIUM 2) - IA2639
This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.
IMMUNOASSAY PREMIUM - LEVEL 3 (IA PREMIUM 3) - IA2640
This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility ofanalytes listed in the package insert.
IMMUNOASSAY PREMIUM - TRI-LEVEL (IA PREMIUM 1, 2 AND 3) - IA2633
This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility ofanalytes listed in the package insert.
IMMUNOASSAY PREMIUM PLUS - LEVEL 1 (IA PREMIUM PLUS 1) - IA3109
This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.
IMMUNOASSAY PREMIUM PLUS - LEVEL 2 (IA PREMIUM PLUS 2) - IA3110
This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.
IMMUNOASSAY PREMIUM PLUS - LEVEL 3 (IA PREMIUM PLUS 3) - IA3111
This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.
IMMUNOASSAY PREMIUM PLUS - TRI-LEVEL (IA PREMIUM PLUS 1, 2 AND 3) - IA3112
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. This material can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.
IMMUNOASSAY SPECIALITY I - LEVEL 1 (IA SPECIALITY I LEV 1) - IAS3113
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. This material can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.
IMMUNOASSAY SPECIALITY I - LEVEL 2 (IA SPECIALITY I LEV 2) - IAS3114
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. This material can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.
IMMUNOASSAY SPECIALITY I - LEVEL 3 (IA SPECIALITY I LEV 3) - IAS3115
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. Thismaterial can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.
IMMUNOASSAY SPECIALITY II - LEVEL 1 (IA SPECIALITY II LEV 1) - IAS3117
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. Thismaterial can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.
IMMUNOASSAY SPECIALITY II - LEVEL 2 (IA SPECIALITY II LEV 2) - IAS3118
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. Thismaterial can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.
IMMUNOASSAY SPECIALITY II - LEVEL 3 (IA SPECIALITY II LEV 3) - IAS3119
IMMUNOGLOBULIN LIQUID PROTEIN CALIBRATOR (IG CAL)
IMMUNOGLOBULIN LIQUID PROTEIN CALIBRATOR (IG CAL) - IT3861
INORGANIC PHOSPHOROUS (PHOS)
INORGANIC PHOSPHOROUS (PHOS) - PH8048
INORGANIC PHOSPHOROUS (PHOS)
INORGANIC PHOSPHOROUS (PHOS) - PH8328
An inorganic phosphorous test system is a device intended for the quantitative in vitro determination of inorganic phosphorous concentration in serum and urine.
INORGANIC PHOSPHOROUS (PHOS) - PH3872
IRON (Fe)
IRON (Fe) - SI8049
IRON (Fe)
IRON (Fe) - SI8330
The product is intended for use in the measurement of urine samples.
ISE DIL - RX4049
The product is required for urine samples. Urine samples must be diluted by a factor of 10 to perform urine measurement. The host analyser will mix the diluent and sample before dispensing the diluted sample into the ISE module.
ISE DIL URN - RX3950
Used as a Calibrator in a two-point calibration. L Solution is pumped into the sample port by the L Solution pump and then positioned in front of the sensor.
L SOLN - D400-0018
Used as a Calibrator in a two-point calibration. L Solution is pumped into the sample port by the L Solution pump and then positioned in front of the sensor.
L SOLN - RX4044
The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
LCO2-2 - CD4006
The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
LCO2-2 - CD8357
LD opt. (LDH L-P)
LD opt. (LDH L-P) - LD8052
LD opt. (LDH L-P)
LD opt. (LDH L-P) - LD8323
LD opt. (LDH P-L)
LD opt. (LDH P-L) - LD8051
LD opt. (LDH P-L)
LD opt. (LDH P-L) - LD8322
The LDH method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of lactate dehydrogenase activity in serum or plasma.
LDH - LD2812
A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum or plasma.
LDH L-P - LD7963
A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum.
LDH L-P - LD3842
A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum or plasma.
LDH P-L - LD3818
A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum or plasma.
LDH P-L - LD401
In Vitro device for the quantitative determination of LDL-Cholesterol in serum and plasma.
LDL - CH3841
LEUCINE ARYLAMIDASE (LAP)
LEUCINE ARYLAMIDASE (LAP) - LA561
The product is intended for the quantitative in vitro determination of Lithium in serum.
Li 2 - LM4005
LIPASE (LPS)
LIPASE (LPS) - LI8050
LIPASE (LPS)
LIPASE (LPS) - LI8361
A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma
LIPASE (LPS) - LI3837
For the quantitative in vitro determination of Lipase in human serum and plasma.
LIPASE (LPS) - LI7979
This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.
LIPID CONTROL - LEVEL 1 (LPD CONTROL 1) - LE2661
This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.
LIPID CONTROL - LEVEL 1 (LPD CONTROL 1) - LE2668
This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.
LIPID CONTROL - LEVEL 2 (LPD CONTROL 2) - LE2662
This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.
LIPID CONTROL - LEVEL 2 (LPD CONTROL 2) - LE2669
This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.
LIPID CONTROL - LEVEL 3 (LPD CONTROL 3) - LE2663
This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems.
LIPID CONTROL - LEVEL 3 (LPD CONTROL 3) - LE2670
Lipid Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Beckman Coulter AU Systems for HDL, LDL and Triglycerides.
LIPID LINEARITY VERIFIERS (For Beckman Coulter AU Systems) (Lipid LinVer - BC) - LV10364
Lipid Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for Cholesterol, HDL, LDL and Triglycerides.
LIPID LINEARITY VERIFIERS (For Roche Systems) (LLV-R) - LV10344
LIPOPROTEIN (a) (Lp (a))
LIPOPROTEIN (a) (Lp (a)) - LP8054
LIPOPROTEIN (a) (Lp (a))
LIPOPROTEIN (a) (Lp (a)) - LP8324
Randox Lipoprotein(a) level 3 control is based on lyophilised human serum containing Lipoprotein(a).
LIPOPROTEIN (a) CONTROL (Lp (a) CONTROL 3) - LP3406
LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM – LEVEL 2 (LIQ CHEM ASY PREMIUM 2)
LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM – LEVEL 2 (LIQ CHEM ASY PREMIUM 2) - LAN4216
LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM – LEVEL 3 (LIQ CHEM ASY PREMIUM 3)
LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM – LEVEL 3 (LIQ CHEM ASY PREMIUM 3) - LAE4217
This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Liquid Assayed Chemistry Control Premium Plus is for the control of accuracy.
LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS - LEVEL 1 (LIQ CHEM ASY PREMIUM PL - LAL4213
This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Liquid Assayed Chemistry Control Premium Plus is for the control of accuracy.
LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS - LEVEL 2 (LIQ CHEM ASY PREMIUM PL - LAN4214
This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Liquid Assayed Chemistry Control Premium Plus is for the control of accuracy.
LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS - LEVEL 3 (LIQ CHEM ASY PREMIUM PL - LAE4215
LIQUID BILIRUBIN CONTROL - LEVEL 1 (LIQ BIL CONTROL 1)
LIQUID BILIRUBIN CONTROL - LEVEL 1 (LIQ BIL CONTROL 1) - BR10172
LIQUID BILIRUBIN CONTROL - LEVEL 2 (LIQ BIL CONTROL 2)
LIQUID BILIRUBIN CONTROL - LEVEL 2 (LIQ BIL CONTROL 2) - BR10173
LIQUID CHEMISTRY PREMIUM - LEVEL 2 (LIQ CHEM PREMIUM 2)
LIQUID CHEMISTRY PREMIUM - LEVEL 2 (LIQ CHEM PREMIUM 2) - LUN5048
LIQUID CHEMISTRY PREMIUM - LEVEL 3 (LIQ CHEM PREMIUM 3)
LIQUID CHEMISTRY PREMIUM - LEVEL 3 (LIQ CHEM PREMIUM 3) - LUE5049
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 1 (LIQ CHEM PREMIUM PLUS 1)
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 1 (LIQ CHEM PREMIUM PLUS 1) - LUL5069
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 1 (LIQ CHEM PREMIUM PLUS 1)
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 1 (LIQ CHEM PREMIUM PLUS 1) - LUL5093
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 2 (LIQ CHEM PREMIUM PLUS 2)
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 2 (LIQ CHEM PREMIUM PLUS 2) - LUN5070
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 2 (LIQ CHEM PREMIUM PLUS 2)
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 2 (LIQ CHEM PREMIUM PLUS 2) - LUN5094
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 3 (LIQ CHEM PREMIUM PLUS 3)
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 3 (LIQ CHEM PREMIUM PLUS 3) - LUE5071
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 3 (LIQ CHEM PREMIUM PLUS 3)
LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 3 (LIQ CHEM PREMIUM PLUS 3) - LUE5095
This product is intended for in vitro diagnostic use in the quality control of CRP on clinical chemistry systems.
LIQUID CRP CONTROL - LEVEL 2 (CRP CONTROL 2) - CP2480
This product is intended for in vitro diagnostic use, in the quality control of CRP on clinical chemistry systems.
LIQUID CRP CONTROL - LEVEL 3 (CRP CONTROL 3) - CP2481
LIQUID CSF CONTROL - LEVEL 1 (CSF CONTROL 1)
LIQUID CSF CONTROL - LEVEL 1 (CSF CONTROL 1) - CF10138
LIQUID CSF CONTROL - LEVEL 2 (CSF CONTROL 2)
LIQUID CSF CONTROL - LEVEL 2 (CSF CONTROL 2) - CF10139
Intended for in vitro diagnostic (IVD) use as a quality control material for determination of Total Bilirubin and Direct Bilirubin on chemistry analysers. For use in a clinical laboratory setting by trained personnel.
LIQUID FROZEN BILIRUBIN CONTROL - LEVEL 1 (LIQ BIL CONTROL 1) - BR10442
Intended for in vitro diagnostic (IVD) use as a quality control material for determination of Total Bilirubin and Direct Bilirubin on chemistry analysers. For use in a clinical laboratory setting by trained personnel.
LIQUID FROZEN BILIRUBIN CONTROL - LEVEL 2 (LIQ BIL CONTROL 2) - BR10443
LIQUID FROZEN LIPID CONTROL - LEVEL 1 (LIQ LPD CONTROL 1)
LIQUID FROZEN LIPID CONTROL - LEVEL 1 (LIQ LPD CONTROL 1) - LE10174
LIQUID FROZEN LIPID CONTROL - LEVEL 2 (LIQ LPD CONTROL 2)
LIQUID FROZEN LIPID CONTROL - LEVEL 2 (LIQ LPD CONTROL 2) - LE10175
LIQUID FROZEN LIPID CONTROL - LEVEL 3 (LIQ LPD CONTROL 3)
LIQUID FROZEN LIPID CONTROL - LEVEL 3 (LIQ LPD CONTROL 3) - LE10176
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Glycated Haemoglobin (HbA1c) on clinical chemistry systems.
Liquid Glycated Haemoglobin (HbA1c) Control Level 1 (LIQ HbA1c CONTROL LEVEL 1) - HA10224
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Glycated Haemoglobin (HbA1c) on clinical chemistry systems.
Liquid Glycated Haemoglobin (HbA1c) Control Level 2 (LIQ HbA1c CONTROL LEVEL 2) - HA10225
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Glycated Haemoglobin (HbA1c) on clinical chemistry systems.
Liquid Glycated Haemoglobin (HbA1c) Control set (LIQ HbA1c CONTROL) - HA10155
The Randox Liquid Immunoassay Premium - Tri-Level are liquid controls developed for use in the quality control of quantitative assays statedin this package insert.
LIQUID IMMUNOASSAY PREMIUM - TRI-LEVEL (LIQ IA PREMIUM 1, 2 AND 3) - LIA3108
For the quantitative in vitro determination of D-3-Hydroxybutyrate in serum and plasma.
LIQUID RANBUT (RBT) - RB4067
For the quantitative in vitro determination of D-3-Hydroxybutyrate in serum and plasma.
LIQUID RANBUT (RBT) - RB8378
The Randox Liquid Urine Control Level 2 is intended for in vitro diagnostic use, in the quality control of Amylase, Calcium, Chloride,Cortisol, Creatinine, Glucose, hCG pregnancy, Magnesium, Microalbumin, Osmolality, pH, Phosphate Inorganic, Potassium,Protein Total, Sodium, Specific Gravity, Urea and Uric Acid (Urate) on clinical chemistry systems. The Liquid Urine Control is for thecontrol of accuracy.
LIQUID URINE CONTROL - LEVEL 2 (LIQ URN CONTROL 2) - UC5074
The Randox Liquid Urine Control - Level 3 is intended for in vitro diagnostic use, in the quality control of Amylase, Calcium, Chloride,Cortisol, Creatinine, Glucose, hCG pregnancy, Magnesium, Microalbumin, Osmolality, pH, Phosphate Inorganic, Potassium,Protein Total, Sodium, Specific Gravity, Urea and Uric Acid (Urate) on clinical chemistry systems. The Liquid Urine Control is for thecontrol of accuracy.
LIQUID URINE CONTROL - LEVEL 3 (LIQ URN CONTROL 3) - UC5075
L-LACTATE (LAC)
L-LACTATE (LAC) - LC2389
L-LACTATE (LAC)
L-LACTATE (LAC) - LC3980
For the quantitative in vitro determination of Lipoprotein (a) in human serum or plasma.
Lp (a) - LP2878
Immunoturbidimetric assay for the quantitative in vitro determination of Lipoprotein(a) in human serum or plasma.
Lp (a) - LP2757
Immunoturbidimetric assay for the quantitative in vitro determination of Lipoprotein(a) in human serum or plasma.
Lp (a) - LP3403
This product is intended for use in the calibration of Lipoprotein(a) assays.
Lp(a) CAL SET - LP3404
MAGNESIUM (Mg)
MAGNESIUM (Mg) - MG3880
MAGNESIUM (Mg)
MAGNESIUM (Mg) - MG8326
A Microalbumin test system is a device intended for the quantitative in vitro determination of Microalbumin concentration in human urine
mALB - MA2864
A Microalbumin test system is a device intended for the quantitative in vitro determination of Microalbumin concentration in urine
mALB - MA3828
A Microalbumin test system is a device intended for the quantitative in vitro determination of Microalbumin concentration in urine
mALB - MA8325
The product is intended to be used for the quantitative in vitro determination of Microalbumin in urine.
mALB - MA2423
The product is intended to be used for the quantitative in vitro determination of Microalbumin in urine.
mALB - MA2426
This product is intended for in vitro use, in the quality control of Alpha-fetoprotein, Free Beta hCG, Free Estriol, Human Chorionic Gonadotropin, Inhibin A and PAPP-A methods on clinical chemistry systems.
MATERNAL CONTROL - LEVEL 1 (MATERNAL CONTROL 1) - MSS5024
This product is intended for in vitro use in the quality control of Alpha-fetoprotein, Free Beta HCG, Free Estriol, Human Chorionic Gonadotrophin, Inhibin A and PAPP-A methods on clinical chemistry systems.
MATERNAL CONTROL - LEVEL 2 (MATERNAL CONTROL 2) - MSS5025
This product is intended for in vitro use in the quality control of Alpha-fetoprotein, Free Beta HCG, Free Estriol, Human Chorionic Gonadotrophin, Inhibin A and PAPP-A methods on clinical chemistry systems.
MATERNAL CONTROL - LEVEL 3 (MATERNAL CONTROL 3) - MSS5026
The MDMA assay is an in vitro diagnostic reagent. For the qualitative and semi-quantitative analysis of MDMA in human urine.
MDMA - DA4014
The Randox Ecstasy Calibrator Set is intended for use in the calibration of the Ecstasy assay.
MDMA CAL - DA2701
The Randox Ecstasy Control Level 1 is intended for use in the Quality Control of the Ecstasy assay. The Ecstasy Control Level 1 contains the specific drug MDMA (3,4-methylenedioxymethamphetamine).
MDMA CONTROL 1 - DA3125
The Randox Ecstasy Control Level 2 is intended for use in the Quality Control of the Ecstasy assay. The Ecstasy Control Level 2 contains the specific drug MDMA (3,4-methylenedioxymethamphetamine).
MDMA CONTROL 2 - DA3126
The Methadone assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of methadone in human urine.
MDONE - DA4016
The Methamphetamine assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of methamphetamine in human urine.
METHAMP - DA4007
MICROALBUMIN (mALB)
MICROALBUMIN (mALB) - MA8056
MICROALBUMIN CALIBRATOR SERIES (mALB CAL)
MICROALBUMIN CALIBRATOR SERIES (mALB CAL) - MA1567
Immunoturbidimetric assay for the quantitative in vitro determination of Myoglobin in human serum.
MYO - MY2127
This product is intended for use in the calibration of Myoglobin immunoturbidimetric assays.
MYO CAL SET - MY2456
This product is intended for the quantitative in vitro determination of Sodium in serum
Na - NA8327
This product is intended for the quantitative in vitro determination of Sodium in serum and plasma
Na - NA3851
This product is intended for the quantitative in vitro determination of Sodium in serum and plasma
Na - NA7167
For the quantitative in vitro determination of Ammonia in plasma.
NH3 - AM3979
Non-Esterified Fatty Acids (NEFA)
Non-Esterified Fatty Acids (NEFA) - FA115
This product should be used in conjunction with RX daytona plus reagents to dilute samples prior to assay.
NS - SA8396
This product should be used in conjunction with RX series reagents to dilute samples prior to assay
NS - SA3854
The Opiates assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of Opiates in human urine.
OPIAT - DA4012
A Pancreatic α‑Amylase test system is a device intended for the quantitative in vitro determination of Pancreatic α‑Amylase activity in serum, plasma or urine.
P AMY - AY2862
A Pancreatic α‑Amylase test system is a device intended for the quantitative in vitro determination of Pancreatic α‑Amylase activity in serum, plasma or urine.
P AMY - AY3855
The device is intended for the quantitative in vitro determination of pancreatic α amylase in serum, plasma and urine.
P AMY - AY7934
PARATHYROID HORMONE CONTROL - LEVEL 1 (PTH CONTROL 1)
PARATHYROID HORMONE CONTROL - LEVEL 1 (PTH CONTROL 1) - PTH10110
PARATHYROID HORMONE CONTROL - LEVEL 2 (PTH CONTROL 2)
PARATHYROID HORMONE CONTROL - LEVEL 2 (PTH CONTROL 2) - PTH10111
PARATHYROID HORMONE CONTROL - LEVEL 3 (PTH CONTROL 3)
PARATHYROID HORMONE CONTROL - LEVEL 3 (PTH CONTROL 3) - PTH10112
Intended for the quantitative in vitro determination of Phenobarbital in human serum.
PHB - TD3408
The device is intended for the quantitative in vitro determination of Phenytoin in human serum
PHT - TD3409
For the quantitative in vitro determination of Potassium in serum or plasma.
Potassium (K) - PT3852
For the quantitative in vitro determination of Potassium in serum or plasma.
Potassium (K) - PT7168
A prealbumin (transthyretin) test system is a device intended for the quantitative in vitro determination of prealbumin (transthyretin) concentration in serum.
PREALBUMIN (PreALB) - PA3843
The Precision Check Solution is used for checking proper functioning of the reagent and sample fluid metering and photometric measuring system.
PRECISION CHECK SOLUTION (PREC) - RX8142
The Pre eclampsia Control Level 1 is intended for use with in vitro diagnostic assays for the quantitative determination of placental growth factor (PlGF) and soluble fms like tyrosine kinase 1 (sFlt 1) in human serum and plasma. The Pre eclampsia Control Level 1 is assayed with target values and are suitable for use on various analysers. The Pre eclampsia Control Level 1 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
PRE-ECLAMPSIA CONTROL LEVEL 1 - PE10527
The Pre eclampsia Control Level 2 is intended for use with in vitro diagnostic assays for the quantitative determination of placental growth factor (PlGF) and soluble fms like tyrosine kinase 1 (sFlt 1) in human serum and plasma. The Pre eclampsia Control Level 2 is assayed with target values and are suitable for use on various analysers. The Pre eclampsia Control Level 2 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
PRE-ECLAMPSIA CONTROL LEVEL 2 - PE10528
The Pre eclampsia Control Level 3 is intended for use with in vitro diagnostic assays for the quantitative determination of placental growth factor (PlGF) and soluble fms like tyrosine kinase 1 (sFlt 1) in human serum and plasma. The Pre eclampsia Control Level 3 is assayed with target values and are suitable for use on various analysers. The Pre eclampsia Control Level 3 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
PRE-ECLAMPSIA CONTROL LEVEL 3 - PE10529
The Reagent Precision Test is used on the RX series clinical chemistry systems for checking proper functioning of the reagent fluid metering and photometric measuring system.
RABS - RP3857
The Reagent Precision Test is used on the RX series clinical chemistry systems for checking proper functioning of the reagent fluid metering and photometric measuring system.
RABS - RP8398
The RANDOX evidence® system is a fully automated, continuous access immunoanalyser using protein biochip array technology. It is intended for the in-vitro qualitative, semi-quantitative or fully quantitative determination of various diagnostic markers.
Randox Evidence™ - EV3600
This product is intended for in vitro diagnostic use, in the calibration of the Randox Ransel assay.
RANSEL CALIBRATOR (RANSEL CAL) - SC10154
This product is intended for in vitro diagnostic use in the control of the Randox Ransel assay.
RANSEL CONTROL - SC692
The Ransod Control is intended for use with in vitro diagnostic assays for the quantitative determination of superoxide dismutase.
RANSOD CONTROL - SD126
This is required for the dilution of heparinized or EDTA whole blood samples for use with the Randox Ransod Reagent.
RANSOD DILUENT (RANSOD DIL) - SD124
Chemiluminescent substrate comprised of 1 bottle of Luminol Reagent - EV701 and 1 bottle of Peroxide Reagent. The analyser uses a 1:1 mixture of the two solutions as a working signal reagent - EV701 to generate a chemiluminescent signal which can be detected by the imaging module of the Evidence™ analyser.
REAG SGNL - EV701 - EV3601
Chemiluminescent substrate comprised of 1 bottle of Luminol Reagent - EV805 and 1 bottle of Peroxide Reagent. The analyser uses a 1:1 mixture of the two solutions as a working signal reagent to generate a chemiluminescent signal which can be detected by the imaging module of the Evidence™ analyser.
REAG SGNL - EV805 - EV3529
This is required for measuring reference electrode potential of an ion selective electrode module.
REF SOLN - RX4045
A RF test system is a device intended for the quantitative in vitro determination of Rheumatoid Factors (RF) concentration in serum.
RF - RF3836
Latex agglutination slide test for the qualitative and semi quantitative in vitro determination of Rheumatoid Factor in serum.
RF - RF1436
The product is a latex agglutination slide test for the qualitative and semi quantitative in vitro determination of Rheumatoid Factor in serum.
RF - RF2716
The product is a latex agglutination slide test for the qualitative and semi quantitative in vitro determination of Rheumatoid Factor in serum.
RF - RF7980
The product is a latex agglutination slide test for the qualitative and semi quantitative in vitro determination of Rheumatoid Factor in serum.
RF - RF7981
This product is intended for us as a latex enhanced immunoturbidimetric test for the quantitative in vitro determination of Rheumatoid Factor in serum.
RF - RF2881
This product is intended for in vitro diagnostic use in the calibration of RF on clinical chemistry analysers.
RF CAL - RF2301
Rheumatoid Factor Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for Rheumatoid Factor (RF).
RHEUMATOID FACTOR LINEARITY VERIFIERS (For Roche Systems) (RFLV) - LV10343
RX Daytona is an automated clinical chemistry analyser complete with dedicated analyser software.
RX daytona - RX3900
The Randox RX daytona plus with ISE is a fully automated, random access, clinical chemistry analyser completewith dedicated analyser software.
RX daytona plus - RX4040
The Randox RX daytona plus without ISE is a fully automated, random access, clinical chemistry analyser completewith dedicated analyser software.
RX daytona plus - RX4041
Rx Imola is an automated clinical chemistry analyser complete with dedicated analyser software.
RX imola - RX4900
The RX monaco Analyser is a fully automated clinical chemistry analyser that has been designed and developed to be operated in a wide range of laboratory settings within different industries. These include clinical, hospital, academic, research and development, veterinary, food and wine laboratories.The RX monaco can detect a wide range of analytes in various liquid matrices. These include serum, plasma, urine, CSF and supernatants.The RX monaco is designed to be used by qualified laboratory staff, in conjunction with current Randox clinical chemistry reagents, to generate a result. The results that are generated are intended to be interpreted by a trained professional to aid in the diagnosis or interpretation of its application.The RX monaco is supplied with dedicated software that has been designed to assist and guide the operator through the operational processes. The software allows the RX monaco to interface with a host system or computer to assist in the processing, storing, ordering and managing of tests and test results.
RX monaco - RX5000
This product is used for checking proper functioning of the sample fluid metering system as well as the photometric measuring system.
SABS - SP3856
This product is used for checking proper functioning of the sample fluid metering system as well as the photometric measuring system.
SABS - SP8399
For the quantitative in vitro determination of Salicylate in human serum
SAL - SAL4024
"SARS-CoV-2 (Severe acute respiratory syndrome coronavirus) Negative/Non-Reactive ControlSARS-CoV-2 Negative/Non-Reactive Control is intended for use with in vitro assays for determination of Total antibodies to SARS-CoV-2 (Severe acute respiratory syndrome coronavirus).SARS-CoV-2 Negative/Non-Reactive Control is unassayed without target values and is suitable for use on various analysers. SARS-CoV-2 Negative/Non-Reactive Control is useful in determining the precision of testing systems and allows performance monitoring of multiple test systems.SARS-CoV-2 (Severe acute respiratory syndrome coronavirus) Positive/Reactive ControlSARS-CoV-2 Positive/Reactive Control is intended for use with in vitro assays for determination of Total antibodies to SARS-CoV-2 (Severe acute respiratory syndrome coronavirus).SARS-CoV-2 Positive/Reactive Control is unassayed without target values and is suitable for use on various analysers. SARS-CoV-2 Negative/Non-Reactive Control is useful in determining the precision of testing systems and allows performance monitoring of multiple test systems."
SARS CoV-2 Controls (SARS-CoV-2) - COV10460
Serology I Postive Control is intended for use with in vitro assays for determination of antibodies to Human Immunodeficiency Virus Type 1 and 2 (HIV-1/2), antibodies to Human T-Lymphotropic Virus Type 1 and 2 (HTLV-1/2), antibodies to Hepatitis C Virus (HCV), Hepatitis B Surface Antigen (HBsAg), IgG antibodies to Hepatitis B Core Antibodies (HBc) and IgG antibodies to Treponema pallidum. Serology I Positive Control is unassayed without target values and is suitable for use on many analysers. These controls must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.Serology I Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation.
SEROLOGY I POSITIVE CONTROL (SEROLOGY I CONTROL +) - SR10352
Serology II Positive Control is intended for use with in vitro assays for determination of antibodies to Hepatitis B Surface Antigen (Anti HBs), IgG antibodies to Hepatitis B Core Antibodies (Anti HBc), antibodies to Hepatitis A (Anti HAV) and antibodies to Hepatitis B Envelope (Anti HBe). Serology II Positive Control is unassayed without target values and is suitable for use on many analysers. These controls must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.Serology II Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation.
SEROLOGY II POSITIVE CONTROL (SEROLOGY II CONTROL +) - SR10353
Serology III Positive Control is intended for use with in vitro assays for determination of IgM antibodies to Hepatitis B Core Antigen (HBc IgM) and IgM antibodies to Hepatitis A (HAV IgM). Serology III Positive Control is unassayed without target values and is suitable for use on many analysers. These controls must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.Serology III Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation.
SEROLOGY III POSITIVE CONTROL (SEROLOGY III CONTROL +) - SR10354
Lyme Disease Negative Control is intended for use as an unassayed non-reactive quality assurance reagent, with in vitro assays detecting IgG antibodies to Borrelia burgdorferi and IgM antibodies to Borrelia burgdorferi.
SEROLOGY LYME DISEASE NEGATIVE CONTROL (LYME CONTROL -) - SR10345
Lyme Disease Positive Control is intended for use with in vitro assays, for determination of IgG antibodies to Borrelia burgdorferi and IgM antibodies to Borrelia burgdorferi. Lyme Disease Positive Control is unassayed without target values and is suitable for use on many analysers.
SEROLOGY LYME DISEASE POSITIVE CONTROL (LYME CONTROL +) - SR10346
Serology Negative Control is intended for use as an unassayed non-reactive quality assurance reagent with in vitro assays detecting antibody to Human Immunodeficiency Virus Type 1/2 (anti-HIV-1/2), antibody to Human T-Lymphotropic Virus Type I/II (anti-HTLV-I/II), Human Immunodeficiency Virus P24 Antigen (HIV P24 Ag), antibody to Hepatitis C Virus (anti-HCV), Immunoglobulin M and total antibodies to Hepatitis B core Antigen (HBc-IgM and anti-HBc Total), Hepatitis B Surface Antigen (HBsAg), antibody to Hepatitis B Surface Antigen (anti-HBs), Immunoglobulin M and total antibody to Hepatitis A Virus (HAV-IgM and anti-HAV Total), Hepatitis B Envelope Antigen (HBeAg), antibody to Hepatitis B Envelope Antigen (anti-HBe) and antibodies to Treponema pallidum.Serology Negative Control is unassayed without target values and is suitable for use on many analysers. These controls must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.Serology Negative Control is helpful in determining the precision of testing systems and in identifying sources of variation.
SEROLOGY NEGATIVE CONTROL (SEROLOGY CONTROL -) - SR10351
ToRCH EBV Positive Control is intended for use with in vitro assays for determination of IgG and IgM antibodies to the viral capsid antigen of Epstein-Barr Virus (EBV VCA) and IgG antibodies to the viral polypeptide nuclear antigen of Epstein-Barr Virus (EBV EBNA).ToRCH EBV Positive Control is unassayed without target values and is suitable for use on many analysers. This control must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.ToRCH EBV Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation.
SEROLOGY ToRCH EBV POSITIVE CONTROL (ToRCH EBV CONTROL +) - SR10350
ToRCH IgG Positive Control is intended for use with in vitro assays for determination of IgG antibodies to Cytomegalovirus (CMV), IgG antibodies to Rubella Virus, IgG antibodies to Toxoplasma gondii, IgG antibodies to Herpes Simplex Virus Type 1 and 2, IgG antibodies to Mumps Virus, IgG antibodies to Measles Virus, IgG antibodies to Varicella Zoster Virus, IgG antibodies to Helicobacter pylori IgG antibodies to Treponema pallidum (Syphilis), IgG antibodies to the viral polypeptide nuclear antigen of Epstein-Barr Virus (EBV EBNA). ToRCH IgG Positive Control is unassayed without target values and is suitable for use on many analysers. This control must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.ToRCH IgG Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation.
SEROLOGY ToRCH IgG POSITIVE CONTROL (ToRCH IgG CONTROL +) - SR10348
ToRCH IgM Positive Control is intended for use with in vitro assays for determination of IgM antibodies to Cytomegalovirus (CMV), IgM antibodies to Rubella Virus, IgM antibodies to Toxoplasma gondii, IgM antibodies to Herpes Simplex Virus Type 1 and 2.ToRCH IgM Positive Control is unassayed without target values and is suitable for use on many analysers. This control must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.ToRCH IgM Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation.
SEROLOGY ToRCH IgM POSITIVE CONTROL (ToRCH IgM CONTROL +) - SR10349
ToRCH Negative Control is intended for use as an unassayed non-reactive quality assurance reagent with in vitro assays detecting IgG and IgM antibodies to Cytomegalovirus (CMV), IgG and IgM antibodies to Rubella virus, IgG and IgM antibodies to Toxoplasma gondii, IgG and IgM antibodies to Herpes Simplex Type 1 and 2, IgG antibodies to Mumps Virus, IgG antibodies to Rubeola Virus (Measles), IgG antibodies to Varicella Zoster Virus, IgG antibodies to Helicobacter pylori, IgG antibodies to Treponema pallidum (Syphilis), IgG and IgM antibodies to the Viral Capsid Antigen of Epstein-Barr virus (EBV VCA) and IgG antibodies to the Viral Polypeptide Nuclear Antigen of Epstein-Barr Virus (EBV EBNA IgG).
SEROLOGY ToRCH NEGATIVE CONTROL (ToRCH CONTROL -) - SR10347
SERUM DILUENT (DIL SM)
SERUM DILUENT (DIL SM) - MS5007
Intended for in vitro diagnostic (IVD) use to monitor the instrument’s response in detecting haemolyzed, icteric and lipemic samples.
SERUM INDICES (SERUM INDICES) - SI10448
sLDL CALIBRATOR (sLDL CAL)
sLDL CALIBRATOR (sLDL CAL) - CH5050
sLDL CONTROL - LEVEL 1 (sLDL CONTROL 1)
sLDL CONTROL - LEVEL 1 (sLDL CONTROL 1) - LE5013
sLDL CONTROL - LEVEL 2 (sLDL CONTROL 2)
sLDL CONTROL - LEVEL 2 (sLDL CONTROL 2) - LE5014
sLDL CONTROL - LEVEL 3 (sLDL CONTROL 3)
sLDL CONTROL - LEVEL 3 (sLDL CONTROL 3) - LE5015
This should be run once a day to prevent protein build up or at 8 hour intervals if the ISE module performs more than 50 samples per day. Cleaning solution may be aspirated from a sample cup but the cup must be covered between use to eliminate evaporation and ensure accuracy.
SOLN WASH - RX4003
The Randox Soluble Transferrin Receptors Calibrator Series is intended for use in the calibration of Soluble Transferrin Receptors assays.
SOLUBLE TRANSFERRIN RECEPTORS CALIBRATOR SERIES (STFR CAL) - TF10161
The Randox Soluble Transferrin Receptors controls are intended for use, in the control of Soluble Transferrin Receptors assays.
SOLUBLE TRANSFERRIN RECEPTORS CONTROLS (STFR CONTROL) - TF10162
Liquid Protein Calibrators are an in vitro diagnostic product used for the calibration of Alpha-1-Antitrypsin, Alpha-1-Acid glycoprotein, IgA, IgG and IgM assays that require sample pre-dilution.
SP CAL (LIQ) - IT2692
Liquid Protein Calibrators are an in vitro diagnostic product used for the calibration of ASO, Complement C3, Complement C4, Ceruloplasmin, CRP, Ferritin, Haptoglobin, IgA, IgG, IgM, Prealbumin, RF and Transferrin assays.
SP CAL (LIQ) - IT2691
This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry and immunoassay systems. The Assayed Liquid Protein Controls are for the control of accuracy.
SP CONTROL 1 - PS2682
This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry and immunoassay systems. The Assayed Liquid Protein Controls are for the control of accuracy.
SP CONTROL 2 - PS2683
This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry and immunoassay systems. The Assayed Liquid Protein Controls are for the control of accuracy.
SP CONTROL 3 - PS2684
SPECIFIC PROTEIN CONTROL - LEVEL 1 (SP CONTROL 1)
SPECIFIC PROTEIN CONTROL - LEVEL 1 (SP CONTROL 1) - PS10221
SPECIFIC PROTEIN CONTROL - LEVEL 2 (SP CONTROL 2)
SPECIFIC PROTEIN CONTROL - LEVEL 2 (SP CONTROL 2) - PS10222
SPECIFIC PROTEIN CONTROL - LEVEL 3 (SP CONTROL 3)
SPECIFIC PROTEIN CONTROL - LEVEL 3 (SP CONTROL 3) - PS10223
The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma.
T BIL - BR2361
The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma.
T BIL - BR3859
The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma.
T BIL - BR8307
The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma.
T BIL - BR9766
The TBIL method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of total bilirubin in serum or plasma.
T BIL - BR2802
This product is intended for use in the calibration of therapeutic drug assays.
TDM CAL - TD3417
A Transferrin test system is a device intended for the quantitative in vitro determination of transferrin concentration in serum.
TF - TF3831
Intended for the quantitative in vitro determination of Transferrin in Serum
TF - TF7197
The Cannabinoid assay is an in vitro diagnostic reagent for the qualitative and semi-quantitative analysis of Cannabinoids (THC) in human urine.
THC - DA4010
The Randox Cannabinoid Calibrator Set is intended for use in the calibration of the 11-nor-Δ9-THC-9-COOH (Cannabinoid) assay.
THC CAL - DA2700
The Randox Cannabinoid Control - Level 1 is intended for use in the Quality Control of the 11-nor-Δ9-THC-9-COOH (Cannabinoid) assay. The Cannabinoid Control Level 1 contains the specific drug Cannabinoid.
THC CONTROL 1 - DA3127
The Randox Cannabinoid Control - Level 2 is intended for use in the Quality Control of the 11-nor-Δ9-THC-9-COOH (Cannabinoid) assay. The Cannabinoid Control Level 2 contains the specific drug Cannabinoid.
THC CONTROL 2 - DA3128
For the quantitative in vitro determination of Theophylline in human serum
THEO - TD3412
Therapeutic Drug Markers (TDM) Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of the Roche Systems for Acetaminophen, Amikacin, Carbamazepine, Digoxin, Gentamicin, Lithium, N-Acetylprocainamide, Phenobarbital, Phenytoin, Procainamide, Quinidine, Salicylate, Theophylline, Tobramycin, Valproic Acid and Vancomycin assays.
THERAPEUTIC DRUG MARKERS LINEARITY VERIFIERS (For Roche Systems) - LV10355
For the quantitative in vitro determination of Total Bilirubin in serum and plasma.
TOTAL BILIRUBIN 2 (T BIL 2) - BR8377
A TIBC test system is a device intended for the quantitative in vitro determination of total iron-binding capacity (TIBC) concentration in serum.
TOTAL IRON-BINDING CAPACITY 2 (TIBC_2) - TI8065
A TIBC_2 test system is a device intended for the quantitative in vitro determination of total iron-binding capacity (TIBC) concentration in serum.
TOTAL IRON-BINDING CAPACITY 2 (TIBC_2) - TI4064
A TIBC_2 test system is a device intended for the quantitative in vitro determination of total iron-binding capacity (TIBC) concentration in serum.
TOTAL IRON-BINDING CAPACITY 2 (TIBC_2) - TI8375
For the quantitative in vitro determination of Total Protein in serum and plasma.
TOTAL PROTEIN (TP) - TP245
For the quantitative in vitro determination of Total Protein in serum and plasma.
TOTAL PROTEIN (TP) - TP3869
TOTAL PROTEIN (UP)
TOTAL PROTEIN (UP) - UP8113
For the quantitative in vitro determination of total protein in urine and C.S.F.
TOTAL PROTEIN (UP) - UP1570
TOTAL PROTEIN 2 (TP 2)
TOTAL PROTEIN 2 (TP 2) - TP8066
TOTAL PROTEIN 2 (TP 2)
TOTAL PROTEIN 2 (TP 2) - TP8336
For the quantitative in vitro determination of Total Protein in serum.
TOTAL PROTEIN 2 (TP 2) - TP4001
TOTAL-IRON BINDING CAPACITY (TIBC)
TOTAL-IRON BINDING CAPACITY (TIBC) - TI1010
TOTAL-IRON BINDING CAPACITY (TIBC)
TOTAL-IRON BINDING CAPACITY (TIBC) - TI8331
TRIGLYCERIDES (TRIGS)
TRIGLYCERIDES (TRIGS) - TR8067
TRIGLYCERIDES (TRIGS)
TRIGLYCERIDES (TRIGS) - TR8147
TRIGLYCERIDES (TRIGS)
TRIGLYCERIDES (TRIGS) - TR9780
For the quantitative in vitro determination of Triglycerides in serum and plasma.
TRIGLYCERIDES (TRIGS) - TR210
For the quantitative in vitro determination of triglycerides in serum or plasma.
TRIGLYCERIDES (TRIGS) - TR3823
For the quantitative in vitro determination of Triglycerides in serum or plasma. This product is suitable for Manual use.
TRIGLYCERIDES (TRIGS) - TR1697
For the quantitative in vitro determination of Triglycerides in serum.
TRIGLYCERIDES (TRIGS) - TR8332
This product is intended for in vitro diagnostic use in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems.
TRI-LEVEL CARDIAC CONTROL (CRD CONTROL 1, 2, 3) - CQ3259
This product is intended for in vitro diagnostic use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems.
TRI-LEVEL CARDIAC CONTROL (CRD CONTROL 1, 2, 3) - CQ3100
The product is intended for the quantitative in vitro determination of Iron/UIBC in serum.
UIBC - SI250
UREA
UREA - UR220
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR221
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR3825
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR3873
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR446
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR456
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR457
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR7975
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR7976
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR8334
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
UREA - UR9729
URIC ACID (UA)
URIC ACID (UA) - UA7972
URIC ACID (UA)
URIC ACID (UA) - UA8069
URIC ACID (UA)
URIC ACID (UA) - UA8333
For the quantitative in vitro determination of Uric Acid in serum, plasma and urine.
URIC ACID (UA) - UA230
For the quantitative in vitro determination of Uric Acid in serum, plasma and urine.
URIC ACID (UA) - UA3824
For the quantitative in vitro determination of Uric Acid in serum, plasma and urine.
URIC ACID (UA) - UA3870
This product is intended for in vitro diagnostic use, in the quality control of urine test strips.
URINALYSIS CONTROL - LEVEL 1 (URNAL CONTROL 1) - UC5033
This product is intended for in vitro diagnostic use, in the quality control of urine test strips.
URINALYSIS CONTROL - LEVEL 2 (URNAL CONTROL 2) - UC5034
For the quantitative in vitro determination of Valproic Acid in human serum
VPA - TD3414
Cleaning Solution for the RX series analysers
WASH conc. 1 - RX3963
Cleaning Solution for the RX series analysers
WASH conc. 2 - RX3962
Cleaning Solution for the RX series analysers
WASH conc. 3 - RX3946
The Xanthochromia Negative Control is intended for use with in vitro diagnostic assays for the quantitative determination of Bilirubin and Oxyhaemoglobin for monitoring of Subarachnoid-haemorrhage testing in Cerebrospinal Fluid (CSF) for Xanthochromia using a spectrophotometer. Xanthochromia Negative Control is unassayed without target values and is suitable for use on various UV spectrophotometer analysers.Xanthochromia Negative Control is for use by trained laboratory professionals and can be used in determining theprecision of testing systems and in identifying sources of variation.
XANTHOCHROMIA NEGATIVE CONTROL (XANTHOCHROMIA ) - XN10502
The Xanthochromia Positive Control is intended for use with in vitro diagnostic assays for the quantitative determination of Bilirubin and Oxyhaemoglobin for monitoring of Subarachnoid-haemorrhage testing in Cerebrospinal Fluid (CSF) for Xanthochromia using a spectrophotometer. Xanthochromia Positive Control is unassayed, without target values and is suitable for use on various UV spectrophotometer analysers. Xanthochromia Positive Control is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation.
XANTHOCHROMIA POSITIVE CONTROL (XANTHOCHROMIA ) - XN10505
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