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Immunalysis 302UR-0100

by Immunalysis Corporation

Ref 302UR-0100

Immunalysis 302UR-0100 is a device classified as IVD General (EU), Class II (US) made by Immunalysis Corporation, registered in EUDAMED on 31 Aug 2026 (Basic UDI-DI B-00840937101070), cleared under FDA 510(k) K131168 on 17 Jan 2014 and listed in FDA GUDID since 31 Aug 2016 (UDI-DI 00840937101070), active as of 24 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE IVDD 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K131168

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD EUDAMED NumberB-00840937101070 Basic UDI-DI 00840937101070UDI-DIDate31 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00840937101070 UDI-DI Date31 Aug 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK131168 Date17 Jan 2014DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-00840937101070 registered 31 Aug 2026 Active
  • FDA 510(k) K131168 decided 17 Jan 2014 Active
  • FDA GUDID UDI-DI 00840937101070 listed 31 Aug 2016 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K131168
  2. Listed FDA GUDID 00840937101070
  3. Registered EUDAMED B-00840937101070

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDD Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Immunalysis
Generic name
Oxycodone IVD, kit, enzyme immunoassay (EIA)
Model / Ref / Catalog
302UR-0100
Primary DI / UDI-DI
00840937101070
Basic UDI-DI
B-00840937101070
510(k) Number
FDA product code
DJG
EMDN code
W0102090123 Oxycodine
GMDN term
Oxycodone IVD, kit, enzyme immunoassay (EIA)
Device class
Class IVD General EUDAMED
Class II GUDID
Regulation number
862.3650
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: Oxycodone IVD, kit, enzyme immunoassay (EIA)

Cleared under the same submission (K131168)

and 1 more cleared under K131168

Similar devices in this category

Other devices filed under OXYCODINE.

Other devices from Immunalysis Corporation

See all devices from Immunalysis Corporation →

Properties

  • Contains animal tissues or cells
  • Reagent
  • IVD kit
  • Professional testing
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)