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Kit De Perfusion

by France Partenaires Medical 2 variants

Ref KP-VVP3004

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 Number376037126/PERF-126 Basic UDI-DI 03760371262991UDI-DIDate12 Jun 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  • Withdrawn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
Kit De Perfusion
Model / Reference
KP-VVP3004
Primary DI / UDI-DI
03760371262991
Basic UDI-DI
376037126/PERF-126
EMDN Code
A070103 Infusion tubing adapters and connectors
Device Class
Class I
Medical Purpose
Kit de perfusion voie veineuse périphérique

Manufacturer details

EUDAMED SRN
FR-PR-000016364

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Properties

  • Sterile