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Set Preparation Radio Marquage

by Hemodia SAS 2 variants

Ref 9535_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 Number3661379ASS30EXM2AML Basic UDI-DI 03661379256169UDI-DIDate28 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  • Withdrawn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 EXAMENS ET SOINS EN IMAGERIE NON STE
Model / Reference
9535_A
Primary DI / UDI-DI
03661379256169
Basic UDI-DI
3661379ASS30EXM2AML
EMDN Code
Z11019099 Various radiotherapy and radiosurgery instruments - other
Device Class
Class IIa
Medical Purpose
Les assemblages de la gamme ‘Examens et soins en imagerie’ sont destinés à : Être utilisés pour la prise en charge de la préparation à un examen nécessitant l'utilisation d'un appareil d'imagerie médicale (ex: Scanner, échographe, IRM, …) hors angiographie. Destiné également aux soins réalisés sous imagerie médicale (ex: Infiltration, …) hors angiographie.

Manufacturer details

EUDAMED SRN
FR-PR-000007189

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See all devices from Hemodia SAS →

Properties

Other properties (1)

  • Sterile: No