6
MaxPlus, MaxGuard - MP9208
Device Description
A collection of tubing and connectors intended to establish an extension of tubing where the standard length of the tubing in an intravenous (IV) administration set is insufficient. This is a single-use device.
Environmental Conditions
No Data Available
Device Sizes
No Data Available
Device Sterilization
Device Sterile: True
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: FPA
Device Name: Set, Administration, Intravascular
Device Class: 2
Physical State: N/A
Definition: N/A
Submission Type ID: 1
Review Panel: HO
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: N/A
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: N/A
Regulation Number: 880.5440
Third Party Flag: Y
Medical Specialty: HO
Device IdentifiersDevice Id: 20885403428026
Device Type: Package
DeviceId Issuing Agency: GS1
Contains DI Number: 10885403428029
Package Quantity: 600
Package Discontinue Date: 1/4/2022 12:00:00 AM
Package Status: Not in Commercial Distribution
Package Type: Case
Device Id: 10885403428029
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A
Device Id: 50885403428027
Device Type: Package
DeviceId Issuing Agency: GS1
Contains DI Number: 10885403428029
Package Quantity: 50
Package Discontinue Date: 1/4/2022 12:00:00 AM
Package Status: Not in Commercial Distribution
Package Type: Shelfpack