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Uricult

by Aidian Oy

Ref 67404

Uricult (67404) is a device classified as IVD General made by Aidian Oy, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-06438115001478), active as of 7 Nov 2026.

Active European Union

CE IVDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-06438115001478 Basic UDI-DI Date6 Nov 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDD Active

Specification

EUDAMED

Model / reference
67404
Primary DI / UDI-DI
06438115001478, 06438115000242
Basic UDI-DI
B-06438115001478, B-06438115000242
EMDN code
W0104010703 Urine screening manual (dipslides etc.)
Device class
Class IVD General
EU registration type
Legacy device (under a directive)
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000023611

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Properties

  • Contains animal tissues or cells
  • Contains substances of microbial origin
  • IVD kit
  • Near-patient testing
  • Professional testing
Other properties (7, all answered No)