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Alinity

FDA UDI

Class I (US FDA UDI)

by Abbott

Identity

Trade Name
Alinity FDA UDI
Generic Name
Laboratory instrument/analyser application software IVD FDA UDI
Device Name
Alinity c CRP HS Assay File FDA UDI
Model / Reference
07P565B FDA UDI
Description
Alinity c CRP HS Assay File FDA UDI

Identifiers

Catalog Number
07P565B FDA UDI
Primary DI / UDI-DI
00380740199371 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Laboratory instrument/analyser application software IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laboratory instrument/analyser application software IVD

Alinity by Abbott — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory instrument/analyser application software IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott

Sources (1)

  • FDA UDI 357181eb-7fda-4ae5-8fe9-853e02153776 35 fields · synced May 30, 2026