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CPAP + (L) with FiO2 and noise reducer

by Vygon

Ref V08776625

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 Number3660812A0400005HF Basic UDI-DI 03660812155885UDI-DIDate4 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  • Withdrawn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 pour voies respiratoires - non stérile
Model / Reference
V08776625
Primary DI / UDI-DI
03660812155885
Basic UDI-DI
3660812A0400005HF
EMDN Code
R02010401 Cpap circuits
Device Class
Class IIa
Medical Purpose
Ces kits sont destinés à aider les patients qui ont besoin d'oxygène. L'indication médicale fournie est exactement la même pour tous les kits CPAP Boussignac

Manufacturer details

EUDAMED SRN
FR-PR-000001873

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Properties

Other properties (1)

  • Sterile: No