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CDC maximum barrier protection

by Vygon

Ref 96.93.0191

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 Number3660812A0400045HT Basic UDI-DI 03660812181648UDI-DIDate20 Jul 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  • Withdrawn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 De Pose De Cvc
Model / Reference
96.93.0191
Primary DI / UDI-DI
03660812181648
Basic UDI-DI
3660812A0400045HT
EMDN Code
C010299 Central venous catheters - other
Device Class
Class IIa
Medical Purpose
Les composants contenus dans les différentes variantes de Vyset correspondent de façon totale ou partielle aux composants nécessaires afin d’élaborer la procédure. Les Vyset de pose de cathéter veineux central peuvent ou non contenir les cathéters veineux centraux

Manufacturer details

EUDAMED SRN
FR-PR-000001873

Other devices from Vygon Corp.

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Properties

  • Sterile