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Alinity 07P6801

by Abbott

Part of a family of 7 devices: see the family page

Ref 07P6801

Alinity 07P6801 is a device classified as Class B in the EU and Class II in the US made by Abbott, registered in EUDAMED on 26 Aug 2026 (Basic UDI-DI 038074AIP0768LS) and listed in FDA GUDID since 30 Jul 2018 (UDI-DI 00380740130343), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE IVDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number038074AIP0768LS Basic UDI-DI 00380740130343UDI-DIDate26 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740130343 UDI-DI Date30 Jul 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038074AIP0768LS registered 26 Aug 2026 Active
  • FDA GUDID UDI-DI 00380740130343 listed 30 Jul 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740130343
  2. Registered EUDAMED 038074AIP0768LS

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Alinity
Generic name
Total testosterone IVD, calibrator
Model / Ref / Catalog
07P6801
Primary DI / UDI-DI
00380740130343
Basic UDI-DI
038074AIP0768LS
FDA product code
JIT
EMDN code
W0102152202 Hormone standards and calibrators
GMDN term
Total testosterone IVD, calibrator
Device class
Class B EUDAMED
Class II GUDID
Regulation number
862.1150
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class B
GUDID
Class II

Device class is stated on each registry's own scale: Class B in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Total testosterone IVD, calibrator

Similar devices in this category

Other devices filed under HORMONE STANDARDS AND CALIBRATORS.

Other devices from Abbott

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Properties

  • Contains animal tissues or cells
  • Reagent
  • IVD kit
  • Professional testing
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (17, all answered No)