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Basic set spinal

by Vygon

Ref 80199.394

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 Number3660812A0400025HM Basic UDI-DI 03660812161237UDI-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  • Withdrawn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

EU market availability

Not listed: EUDAMED names no country where this device is made available.

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

Last checked 27 Oct 2026.

Specification

EUDAMED

Device Name
Vyset De Rachianesthesie
Model / Reference
80199.394
Primary DI / UDI-DI
03660812161237
Basic UDI-DI
3660812A0400025HM
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

  • Sterile