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Set complet de perfusion par gravité avec épicrânienne 22G Vitadomia

by Oxypharm

Ref KH402

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number366506621072091GW Basic UDI-DI 03665066002107UDI-DIDate15 Oct 2024RegisteredStatusActive

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  • Withdrawn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
Sets complets de perfusion par gravité, compatibles veines fragiles
Model / Reference
KH402
Primary DI / UDI-DI
03665066002107
Basic UDI-DI
366506621072091GW
EMDN Code
A0502 Non-elastomeric systems
Device Class
Class IIa
Medical Purpose
Sets de perfusion conçus pour la perfusion intra-veineuse par gravité de solutions parentérales, permettant de sélectionner un débit déterminé (ml/h) qui doit être vérifié par une chambre de goutte-à-goutte

Manufacturer details

EUDAMED SRN
FR-PR-000012308

Other devices from Oxypharm

Properties

Other properties (1)

  • Sterile: No