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Set De Sondage Urinaire

by Hemodia SAS

Ref 9999_A

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDR Number3661379ASS29URO2BVA Basic UDI-DI 03661379281604UDI-DIDate20 May 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Assemblage UROLOGIE STE
Model / Reference
9999_A
Primary DI / UDI-DI
03661379281604
Basic UDI-DI
3661379ASS29URO2BVA
EMDN Code
U99 Devices for urogenital system - other
Device Class
Class IIb
Medical Purpose
Les assemblages de la gamme ‘Urologie’ sont destinés à : Être utilisés pour la prise en charge des examens et des maladies des voies urinaires et de l'appareil génital de l'homme.

Manufacturer details

EUDAMED SRN
FR-PR-000007189

Other devices from Hemodia SAS

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Properties

  • Sterile