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Set PCI SSUCH SLK

by Vygon

Ref 96.93V03

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 Number3660812A0400074J2 Basic UDI-DI 03660812184571UDI-DIDate10 Aug 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  • Withdrawn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 Angio-Coro
Model / Reference
96.93V03
Primary DI / UDI-DI
03660812184571
Basic UDI-DI
3660812A0400074J2
EMDN Code
C01040199 Cardiac angiography devices - other
Device Class
Class III
Medical Purpose
Les Vyset regroupent les composants nécessaires aux différents gestes de la chirurgie radiologique interventionnelle et de procédures cardio-vasculaires (angiographie, coronarographie, faisceaux de His, pose de pace maker, etc).

Manufacturer details

EUDAMED SRN
FR-PR-000001873

Other devices from Vygon Corp.

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Properties

  • Sterile