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Uriki Test K

by Iki France EUDAMED

Ref UT-K, Uriki

EMDN W02010785

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-03770027558033 Basic UDI-DIDate20 Feb 2024RegisteredStatusActive
European UnionCE/IVDR NumberB-03770027558033 Basic UDI-DIDate20 Feb 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDD, CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Trade Name
Uriki Test K
Uriki
Model / Reference
UT-K, Uriki
Primary DI / UDI-DI
03770027558033, 03770027558019
Basic UDI-DI
B-03770027558033, 3770027558UrikiPY
Direct Marketing DI
03770027558019
EMDN Code
W02010785, W020101020101
Device Class
Class IVD General
Class A
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000023181

Other devices from Iki

Properties & raw data

Show properties, registry sources and raw records
  • Reagent YesEUDAMEDNoEUDAMED
  • Near-Patient Testing
  • Surgical Instrument NoEUDAMEDYesEUDAMED
Other properties (8)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • New Device: No

Sources (2)

  • EUDAMED 07704d5c-dad1-4eec-b22e-60b8d911f657 61 fields · synced 22 Oct 2026
  • EUDAMED 03770027558019|3770027558URIKIPY 61 fields · synced 17 May 2026