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Alinity 07P921A

by Abbott

Alinity 07P921A is a Class I device made by Abbott, listed in FDA GUDID since 11 Nov 2020 (UDI-DI 00380740142865), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00380740142865 UDI-DI Date11 Nov 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Alinity
Generic name
Laboratory instrument/analyser application software IVD
Model / Ref / Catalog
07P921A
Primary DI / UDI-DI
00380740142865
FDA product code
JJE
GMDN term
Laboratory instrument/analyser application software IVD
Device class
Class I
Regulation number
862.2160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laboratory instrument/analyser application software IVD

Similar devices in this category

Other devices filed under Laboratory instrument/analyser application software IVD.

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Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)