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Gs

FDA UDI

Class N (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
GS FDA UDI
Generic Name
HIV1 antibody IVD, kit, immunoblot FDA UDI
Device Name
Human Immunodeficiency Virus Type 1 GS HIV-1 Western Blot, (40 Tests) FDA UDI
Model / Reference
32508 FDA UDI
Description
Human Immunodeficiency Virus Type 1 GS HIV-1 Western Blot, (40 Tests) FDA UDI

Identifiers

Catalog Number
32508 FDA UDI
Primary DI / UDI-DI
00847865003049 FDA UDI
FDA Product Code
MVW FDA UDI
GMDN Term
HIV1 antibody IVD, kit, immunoblot FDA UDI

Classification

Device Class
N FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: HIV1 antibody IVD, kit, immunoblot

Gs by Bio-Rad Laboratories — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as HIV1 antibody IVD, kit, immunoblot.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9e90f1ee-55b8-4d0b-a417-619341a61554 37 fields · synced Jun 8, 2026