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Alinity 08P2030

by Abbott

Ref 08P2030

Alinity 08P2030 is a device classified as Class B in the EU and Class II in the US made by Abbott, registered in EUDAMED on 23 Aug 2026 (Basic UDI-DI 038074ACP0820HM) and listed in FDA GUDID since 6 Jun 2018 (UDI-DI 00380740135171), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number038074ACP0820HM Basic UDI-DI 00380740135171UDI-DIDate23 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740135171 UDI-DI Date6 Jun 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038074ACP0820HM registered 23 Aug 2026 Active
  • FDA GUDID UDI-DI 00380740135171 listed 6 Jun 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740135171
  2. Registered EUDAMED 038074ACP0820HM

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  • Withdrawn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 alkaline phosphatase (ALP) IVD, reagent
Model / Ref / Catalog
08P2030
Primary DI / UDI-DI
00380740135171
Basic UDI-DI
038074ACP0820HM
FDA product code
CJE
EMDN code
W01010105 Alkaline phosphatase - total
GMDN term
Total alkaline phosphatase (ALP) IVD, reagent
Device class
Class B EUDAMED
Class II GUDID
Regulation number
862.1050
EU registration type
Standard device
EU market of registration
Ireland
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 alkaline phosphatase (ALP) IVD, reagent

Similar devices in this category

Other devices filed under ALKALINE PHOSPHATASE - TOTAL.

Other devices from Abbott

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Properties

  • Reagent
  • IVD kit
  • Professional testing
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)