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Alinity 08P2220

by Abbott Laboratories

Alinity 08P2220 is a Class I device made by Abbott Laboratories, listed in FDA GUDID since 30 Jul 2018 (UDI-DI 00380740136192), 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 Number00380740136192 UDI-DI Date30 Jul 2018ListedStatusListed 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  • Withdrawn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
Ammonia IVD, kit, spectrophotometry
Model / Ref / Catalog
08P2220
Primary DI / UDI-DI
00380740136192
FDA product code
JIF
GMDN term
Ammonia IVD, kit, spectrophotometry
Device class
Class I
Regulation number
862.1065
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ammonia IVD, kit, spectrophotometry

Other devices from Abbott Laboratories

See all devices from Abbott Laboratories →

Properties

  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)