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Vyset perfusion – set de pose sur voie veineuse centrale – HAD France

by Vygon

Ref V02772203

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 Number3660812A0400015HJ Basic UDI-DI 03660812187633UDI-DIDate4 Aug 2026RegisteredStatusActive

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  • Withdrawn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
Vyset perfusion - non stérile
Model / Reference
V02772203
Primary DI / UDI-DI
03660812187633
Basic UDI-DI
3660812A0400015HJ
EMDN Code
A010199 Needles for infusion and collection - other
Device Class
Class III
Medical Purpose
Les Vyset de soins pour perfusion sont des sets regroupant les composants nécessaires au branchement/débranchement de ligne de perfusion sur les dispositifs d’accès vasculaire moyen et long terme (chambre à cathéter implantable, PICC, Midline et CVC), au rinçage de ces abords vasculaire ainsi qu’à la réfection de pansements.

Manufacturer details

EUDAMED SRN
FR-PR-000001873

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Properties

Other properties (1)

  • Sterile: No