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Architect 04T0401

by Abbott Ireland

Ref 04T0401

Architect 04T0401 is a device classified as Class C in the EU and Class I in the US made by Abbott Ireland, registered in EUDAMED on 24 Oct 2026 (Basic UDI-DI 038074ART0404QJ) and listed in FDA GUDID since 24 Oct 2025 (UDI-DI 00380740204020), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number038074ART0404QJ Basic UDI-DI 00380740204020UDI-DIDate24 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740204020 UDI-DI Date24 Oct 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038074ART0404QJ registered 24 Oct 2026 Active
  • FDA GUDID UDI-DI 00380740204020 listed 24 Oct 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740204020
  2. Registered EUDAMED 038074ART0404QJ

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  • Withdrawn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
Abbott EUDAMED
Architect GUDID
Generic name
Lipase IVD, calibrator
Device name
Lipase2
Model / Ref / Catalog
04T0401
Primary DI / UDI-DI
00380740204020
Basic UDI-DI
038074ART0404QJ
FDA product code
CHI
EMDN code
W0101050302 Calibrators single component (cc)
GMDN term
Lipase IVD, calibrator
Device class
Class C EUDAMED
Class I GUDID
Regulation number
862.1465
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 C
GUDID
Class I

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

Similar devices in this category

Other devices filed under CALIBRATORS SINGLE COMPONENT (CC).

Other devices from Abbott Ireland

See all devices from Abbott Ireland →

Properties

  • Contains human tissues or cells
  • Contains animal tissues or cells
  • Contains substances of microbial origin
  • Reagent
  • IVD kit
  • Professional testing
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (15, all answered No)