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Basic NRFIT set N°002

by Vygon

Ref V05770952

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 Number3660812A0400017HN Basic UDI-DI 03660812183680UDI-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  • Withdrawn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 péri-rachi combiné non stérile
Model / Reference
V05770952
Primary DI / UDI-DI
03660812183680
Basic UDI-DI
3660812A0400017HN
EMDN Code
A01030101 Spinal anaesthesia needles and kits
Device Class
Class III
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

Other properties (1)

  • Sterile: No