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Kit De Perfusion

by France Partenaires Medical 9 variants

Ref KP-1010

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-32A Basic UDI-DI 03760371263158UDI-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  • Withdrawn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

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 29 Oct 2026.

Specification

EUDAMED

Device Name
Kit De Perfusion
Model / Reference
KP-1010
Primary DI / UDI-DI
03760371263158
Basic UDI-DI
376037126/PERF-32A
EMDN Code
A070103 Infusion tubing adapters and connectors
Device Class
Class III
Medical Purpose
KIT DE PERFUSION

Manufacturer details

EUDAMED SRN
FR-PR-000016364

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Properties

  • Sterile