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Architect 1L75-55

by Abbott Laboratories

Ref 01L7555Model 1L75-55

Architect 1L75-55 (01L7555) is a device classified as IVD General (EU), Class II (US) made by Abbott Laboratories, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-00380740001322) and listed in FDA GUDID since 6 Jun 2016 (UDI-DI 00380740001322), 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-00380740001322 Basic UDI-DI 00380740001322UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740001322 UDI-DI Date6 Jun 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00380740001322 registered 30 Oct 2026 Active
  • FDA GUDID UDI-DI 00380740001322 listed 6 Jun 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740001322
  2. Registered EUDAMED B-00380740001322

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  • Withdrawn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
Architect
Generic name
Cyclosporin A/cyclosporine therapeutic drug monitoring IVD, reagent
Device name
Cyclosporine (WB Precip Reagent)
Model / Ref / Catalog
1L75-55, 01L7555
Primary DI / UDI-DI
00380740001322
Basic UDI-DI
B-00380740001322
FDA product code
DLJ, MKW
EMDN code
W0102080601 Cyclosporine total
GMDN term
Cyclosporin A/cyclosporine therapeutic drug monitoring IVD, reagent
Device class
Class IVD General EUDAMED
Class II GUDID
Regulation number
862.3200, 862.1235
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
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: Cyclosporin A/cyclosporine therapeutic drug monitoring IVD, reagent

Similar devices in this category

Other devices filed under IMMUNOSUPPRESSANT TDM.

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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)