Product Overview

HCV Genotype
VERSANT HCV 2.0 LiPA - 10492005


Device Description

A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of Hepatitis C virus nucleic acid in a clinical specimen, using a nucleic acid technique (NAT).


Environmental Conditions

No Data Available


Device Sizes

No Data Available


Device Sterilization

Device Sterile: False

Sterilization Prior To Use: False

Sterilization Methods: No Data Available


Product Codes

Code: OBF

Device Name: Assay, Genotyping, Hepatitis C Virus

Device Class: 2

Physical State: RT-PCR amplification

Definition: In vitro diagnostic device for qualitative detection and classification of 8 clinically relevant Hepatitis C Virus RNA genotypes

Submission Type ID: 1

Review Panel: MI

Review Code: N/A

Technical Method: N

Gmp Exempt Flag: In vitro diagnostic device for qualitative detection and classification of 8 clinically relevant Hepatitis C Virus RNA genotypes

Life Sustain Support Flag: N

Unclassified Reason: N/A

Implant Flag: N

Target Area: Human specimens

Regulation Number: 866.3170

Third Party Flag: N

Medical Specialty: MI


Device Identifiers

Device Id: 00630414602882

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


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