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AlinIQ 03R89-24

by ABBOTT S.r.l.

AlinIQ 03R89-24 (03R8924) is a Class I device made by ABBOTT S.r.l., listed in FDA GUDID since 20 Dec 2019 (UDI-DI 00380740145125), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00380740145125 UDI-DI Date20 Dec 2019ListedStatusListed 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  • Withdrawn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
AlinIQ
Generic name
Laboratory instrument/analyser application software IVD
Model / Ref / Catalog
03R89-24, 03R8924
Primary DI / UDI-DI
00380740145125
FDA product code
JQP
GMDN term
Laboratory instrument/analyser application software IVD
Device class
Class I
Regulation number
862.2100
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.

Other devices from ABBOTT S.r.l.

See all devices from ABBOTT S.r.l. →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)