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Set de perfusion sous cutanee

by Vygon

Ref 96.90.0424

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 Number3660812A0400048HZ Basic UDI-DI 03660812174756UDI-DIDate6 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  • Withdrawn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
Model / Reference
96.90.0424
Primary DI / UDI-DI
03660812174756
Basic UDI-DI
3660812A0400048HZ
EMDN Code
A010199 Needles for infusion and collection - other
Device Class
Class I
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

  • Sterile