Identity

Trade Name
Alinity FDA UDI
Generic Name
Human T-cell lymphotrophic virus 1 & 2 (HTLV1 & HTLV2) antibody IVD, control FDA UDI
Device Name
Alinity s HTLV I/II Assay Control Kit FDA UDI
Model / Reference
06P0715 FDA UDI
Description
Alinity s HTLV I/II Assay Control Kit FDA UDI

Identifiers

Catalog Number
06P0715 FDA UDI
Primary DI / UDI-DI
00380740203641 FDA UDI
GMDN Term
Human T-cell lymphotrophic virus 1 & 2 (HTLV1 & HTLV2) antibody IVD, control 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: Human T-cell lymphotrophic virus 1 & 2 (HTLV1 & HTLV2) antibody IVD, control

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

Similar devices

Also classified as Human T-cell lymphotrophic virus 1 & 2 (HTLV1 & HTLV2) antibody IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d3b559a7-a6b4-451c-a424-7ee8d6c7884f 36 fields · synced Jun 6, 2026