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Vyset peridurale nexus NRFIT Vyflex

by Vygon

Ref V05771185

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3660812A0400033HL Basic UDI-DI 03660812189972UDI-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  • Withdrawn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 POUR ANESTHESIE PERIDURALE non stérile
Model / Reference
V05771185
Primary DI / UDI-DI
03660812189972
Basic UDI-DI
3660812A0400033HL
EMDN Code
A01030102 Epidural anaesthesia needles and kits
Device Class
Class III
Medical Purpose
Les Vyset d’anesthésie péridurale sont des sets regroupant les composants nécessaires aux différentes étapes de la pose d’un cathéter dans l’espace péridurale. Le cathéter de péridurale est indiqué pour effectuer une anesthésie lors d’une chirurgie, ou une analgésie lors d’un accouchement.

Manufacturer details

EUDAMED SRN
FR-PR-000001873

Other devices from Vygon Corp.

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Properties

Other properties (1)

  • Sterile: No