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RVI Basick Pack

by Vygon

Ref V05770907

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 Number3660812A0400024HK Basic UDI-DI 03660812189989UDI-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  • Withdrawn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 Rachianesthesie
Model / Reference
V05770907
Primary DI / UDI-DI
03660812189989
Basic UDI-DI
3660812A0400024HK
EMDN Code
A99 Devices for administration, withdrawal and collection - other
Device Class
Class IIa
Medical Purpose
Les Vyset de Rachianesthésie sont des sets regroupant les composants nécessaires à une procédure de rachianesthésie ou de ponction lombaire. La rachianesthésie consiste à injecter une dose de solution anesthésique dans le liquide céphalo-rachidien afin d’anesthésier l’abdomen, le bassin et les membres inférieurs. La ponction lombaire a pour but de prélever du liquide céphalo-rachidien afin de réaliser des analyses.

Manufacturer details

EUDAMED SRN
FR-PR-000001873

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Properties

  • Sterile