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Alinity

FDA UDI

Class II (US FDA UDI)

by Abbott Laboratories, Inc.

Identity

Trade Name
Alinity FDA UDI
Generic Name
Lithium therapeutic drug monitoring IVD, reagent FDA UDI
Device Name
Alinity c Lithium Reagent Kit 190 Tests FDA UDI
Model / Reference
08P5320 FDA UDI
Description
Alinity c Lithium Reagent Kit 190 Tests FDA UDI

Identifiers

Catalog Number
08P5320 FDA UDI
Primary DI / UDI-DI
00380740136277 FDA UDI
FDA Product Code
NDW FDA UDI
GMDN Term
Lithium therapeutic drug monitoring IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3560 FDA UDI
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

Yes

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: Lithium therapeutic drug monitoring IVD, reagent

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

Similar devices

Also classified as Lithium therapeutic drug monitoring IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8989443f-46b1-4e04-8a65-2dbae5879e34 36 fields · synced May 31, 2026