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Alinity

FDA UDI

Class II (US FDA UDI)

by Abbott Laboratories, Inc.

Identity

Trade Name
Alinity FDA UDI
Generic Name
Alpha-1-antitrypsin (protease inhibitor) IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Alinity c A1-Antitrypsin Reagent Kit 200 Tests FDA UDI
Model / Reference
01R0721 FDA UDI
Description
Alinity c A1-Antitrypsin Reagent Kit 200 Tests FDA UDI

Identifiers

Catalog Number
01R0721 FDA UDI
Primary DI / UDI-DI
00380740153519 FDA UDI
510(k) Number
K050596 FDA UDI
FDA Product Code
DEM FDA UDI
GMDN Term
Alpha-1-antitrypsin (protease inhibitor) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5130 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: Alpha-1-antitrypsin (protease inhibitor) IVD, kit, nephelometry/turbidimetry

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

Similar devices

Also classified as Alpha-1-antitrypsin (protease inhibitor) IVD, kit, nephelometry/turbidimetry.

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 10573312-fd1d-4001-ae64-7cdef46109fc 37 fields · synced May 30, 2026