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Alinity 08P3320

by Abbott Ireland Diagnostics

Ref 08P3320

Alinity 08P3320 is a device classified as IVD General (EU), Class II (US) made by Abbott Ireland Diagnostics, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-00380740130053) and listed in FDA GUDID since 10 Aug 2018 (UDI-DI 00380740130053), active as of 7 Nov 2026.

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

CE IVDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD EUDAMED NumberB-00380740130053 Basic UDI-DI 00380740130053UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740130053 UDI-DI Date10 Aug 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00380740130053 registered 30 Oct 2026 Active
  • FDA GUDID UDI-DI 00380740130053 listed 10 Aug 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740130053
  2. Registered EUDAMED B-00380740130053

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Alinity
Generic name
Total cortisol IVD, kit, chemiluminescent immunoassay
Model / Ref / Catalog
08P3320
Primary DI / UDI-DI
00380740130053
Basic UDI-DI
B-00380740130053
FDA product code
JFT
EMDN code
W0102060203 Cortisol
GMDN term
Total cortisol IVD, kit, chemiluminescent immunoassay
Device class
Class IVD General EUDAMED
Class II GUDID
Regulation number
862.1205
EU registration type
Legacy device (under a directive)
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IVD General
GUDID
Class II

Device class is stated on each registry's own scale: Class IVD General 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 cortisol IVD, kit, chemiluminescent immunoassay

Similar devices in this category

Other devices filed under CORTISOL.

Other devices from Abbott Ireland Diagnostics

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Properties

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