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Immunalysis 10002-15

by Immunalysis Corporation

Ref 10002-15

Immunalysis 10002-15 is an in vitro diagnostic device (EU IVDD general IVD; FDA Class II; FDA product code DKB, Calibrators, drug mixture; EMDN category drugs of abuse / toxicology standards and calibrators) made by Immunalysis Corporation, registered in EUDAMED on 20 Aug 2026 (Basic UDI-DI B-00840937108932) and listed in FDA GUDID since 27 Dec 2016 (UDI-DI 00840937108932), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD EUDAMED NumberB-00840937108932 Basic UDI-DI 00840937108932UDI-DIDate20 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00840937108932 UDI-DI Date27 Dec 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00840937108932 registered 20 Aug 2026 Active
  • FDA GUDID UDI-DI 00840937108932 listed 27 Dec 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00840937108932
  2. Registered EUDAMED B-00840937108932

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  • Withdrawn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
Immunalysis
Generic name
Multiple-type clinical chemistry analyte profile IVD, calibrator
Model / Ref / Catalog
10002-15
Primary DI / UDI-DI
00840937108932
Basic UDI-DI
B-00840937108932
FDA product code
DKB
EMDN code
W0102152209 Drugs of abuse / toxicology standards and calibrators
GMDN term
Multiple-type clinical chemistry analyte profile IVD, calibrator
Device class
Class IVD General EUDAMED
Class II GUDID
Regulation number
862.3200
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
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: Multiple-type clinical chemistry analyte profile IVD, calibrator

Similar devices in this category

Other devices filed under DRUGS OF ABUSE / TOXICOLOGY STANDARDS AND CALIBRATORS.

Other devices from Immunalysis Corporation

See all devices from Immunalysis Corporation →

Properties

  • Contains animal tissues or cells
  • Reagent
  • IVD kit
  • Professional testing
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)