Identity

Trade Name
Alinity FDA UDI
Generic Name
Hepatitis C virus total antibody IVD, kit, chemiluminescent assay FDA UDI
Device Name
Alinity s Anti-HCV II Reagent Kit FDA UDI
Model / Reference
04W5661 FDA UDI
Description
Alinity s Anti-HCV II Reagent Kit FDA UDI

Identifiers

Catalog Number
04W5661 FDA UDI
Primary DI / UDI-DI
00380740203139 FDA UDI
GMDN Term
Hepatitis C virus total antibody IVD, kit, chemiluminescent assay FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Hepatitis C virus total antibody IVD, kit, chemiluminescent assay

Alinity by Abbott Laboratories, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hepatitis C virus total antibody IVD, kit, chemiluminescent assay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a11a975a-e9a4-46cf-ad19-100fe4bfa0e9 36 fields · synced May 30, 2026