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Gs

FDA UDI

Class II (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
GS FDA UDI
Generic Name
HIV1/HIV2 antigen/antibody IVD, control FDA UDI
Device Name
GS HIV Combo Ag/Ab EIA, Negative Control, 1.5 mL FDA UDI
Model / Reference
26220 FDA UDI
Description
GS HIV Combo Ag/Ab EIA, Negative Control, 1.5 mL FDA UDI

Identifiers

Catalog Number
26220 FDA UDI
Primary DI / UDI-DI
00847865013185 FDA UDI
FDA Product Code
MZF FDA UDI
GMDN Term
HIV1/HIV2 antigen/antibody IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3956 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

No

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

Dimensions & Sizes

Size
Total Volume — 1.5 Milliliter FDA UDI

Category: HIV1/HIV2 antigen/antibody IVD, control

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

Similar devices

Also classified as HIV1/HIV2 antigen/antibody IVD, control.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3d40018b-d89d-4b58-b1b7-89619d0b736a 38 fields · synced May 30, 2026