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Architect 1P33-01

by Abbott Laboratories

Ref 01P3301

Architect 1P33-01 (01P3301) is a device classified as Class C in the EU and Class II in the US made by Abbott Laboratories, registered in EUDAMED on 24 Oct 2026 (Basic UDI-DI 038074ARP0133NW) and listed in FDA GUDID since 6 Jun 2016 (UDI-DI 00380740001773), 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 Number038074ARP0133NW Basic UDI-DI 00380740001773UDI-DIDate24 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740001773 UDI-DI Date6 Jun 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038074ARP0133NW registered 24 Oct 2026 Active
  • FDA GUDID UDI-DI 00380740001773 listed 6 Jun 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740001773
  2. Registered EUDAMED 038074ARP0133NW

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  • Withdrawn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
Phenobarbital IVD, calibrator
Device name
ARCHITECT iPhenobarbital
Model / Ref / Catalog
01P3301, 1P33-01
Primary DI / UDI-DI
00380740001773
Basic UDI-DI
038074ARP0133NW
FDA product code
DLJ, DLZ
EMDN code
W0102152201 Tdm/drug standards and calibrators
GMDN term
Phenobarbital IVD, calibrator
Device class
Class C EUDAMED
Class II GUDID
Regulation number
862.3200, 862.3660
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
01P3301
GUDID
1P33-01
Device classEUDAMED
Class C
GUDID
Class II

Device class is stated on each registry's own scale: Class C 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: Phenobarbital IVD, calibrator

Similar devices in this category

Other devices filed under TDM/DRUG STANDARDS AND CALIBRATORS.

Other devices from Abbott Laboratories

See all devices from Abbott Laboratories →

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)