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Cysti'test

by Aaz Productions Le Materiel Biomedical 2 variants

Ref TR-URI-002

Active European Union

CE IVDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-03770011742479 Basic UDI-DI 03770011742479UDI-DIDate30 Sep 2024RegisteredStatusActive

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  • Withdrawn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

Device Name
Cysti’test
Model / Reference
TR-URI-002
Primary DI / UDI-DI
03770011742479
Basic UDI-DI
B-03770011742479
EMDN Code
W0101060204 Urine multi-constituent test strips (manual)
Device Class
Class IVD General
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000015889

Other devices from Aaz Productions Le Materiel Biomedical

See all devices from Aaz Productions Le Materiel Biomedical →

Properties

  • Reagent
  • Near-Patient Testing
  • Professional Testing

Other properties (7)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No