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Alinity 08P6702

by Abbott Laboratories

Alinity 08P6702 is a Class II device made by Abbott Laboratories, listed in FDA GUDID since 4 Jan 2019 (UDI-DI 00380740153717), 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 Number00380740153717 UDI-DI Date4 Jan 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  • Withdrawn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
Alinity
Generic name
Plasma protein IVD, calibrator
Model / Ref / Catalog
08P6702
Primary DI / UDI-DI
00380740153717
FDA product code
JIX
GMDN term
Plasma protein IVD, calibrator
Device class
Class II
Regulation number
862.1150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Plasma protein IVD, calibrator

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Properties

  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)