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Architect 7K77-01

by Abbott Ireland

Part of a family of 8 devices: see the family page

Ref 07K7701

Architect 7K77-01 (07K7701) is a device classified as Class B in the EU and Class II in the US made by Abbott Ireland, registered in EUDAMED on 17 Aug 2026 (Basic UDI-DI 038074EAK0777HY) and listed in FDA GUDID since 9 Sep 2016 (UDI-DI 00380740014889), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number038074EAK0777HY Basic UDI-DI 00380740014889UDI-DIDate17 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740014889 UDI-DI Date9 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038074EAK0777HY registered 17 Aug 2026 Active
  • FDA GUDID UDI-DI 00380740014889 listed 9 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740014889
  2. Registered EUDAMED 038074EAK0777HY

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  • Withdrawn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
Architect
Generic name
Progesterone IVD, calibrator
Device name
ARCHITECT Progesterone
Model / Ref / Catalog
07K7701, 7K77-01
Primary DI / UDI-DI
00380740014889
Basic UDI-DI
038074EAK0777HY
FDA product code
JIT
EMDN code
W0102152208 Standards and calibrators for individual and specific hormones /proteins
GMDN term
Progesterone 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 · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
07K7701
GUDID
7K77-01
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: Progesterone IVD, calibrator

Similar devices in this category

Other devices filed under STANDARDS AND CALIBRATORS FOR INDIVIDUAL AND SPECIFIC HORMONES /PROTEINS.

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
  • Lot / batch number
  • Expiration date
Other properties (16, all answered No)