Alinity 08P6712

by Abbott Laboratories

Alinity 08P6712 is a Class I device made by Abbott Laboratories, listed in FDA GUDID since 4 Jan 2019 (UDI-DI 00380740153724), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00380740153724 UDI-DI	Date4 Jan 2019Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00380740153724

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Alinity
Generic name: Plasma protein IVD, control
Model / Ref / Catalog: 08P6712

Primary DI / UDI-DI: 00380740153724
FDA product code: JJY
GMDN term: Plasma protein IVD, control

Device class: Class I
Regulation number: 862.1660
GUDID distribution status: In Commercial Distribution

Other devices from Abbott Laboratories

Architect

Class A
Alinity

Class A
Architect

Class A
Architect

Class A

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Properties

Prescription use
Convenience kit
Premarket exempt
Lot / batch number
Expiration date

Other properties (10, all answered No)