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Set branchement & débranchement voie veineuse N°1

by Raffin Medical

Ref 405217

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 Number3666002PP-ABO-K5 Basic UDI-DI 03700433505925UDI-DIDate15 May 2023RegisteredStatusActive

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  • Withdrawn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
Sets d'injection, de perfusion, de prélèvement et de dialyse
Model / Reference
405217
Primary DI / UDI-DI
03700433505925
Basic UDI-DI
3666002PP-ABO-K5
EMDN Code
A03040199 Infusion kits (with or w/o pump), single-use - other
Device Class
Class III
Medical Purpose
Sets à façon et à usage unique pour l’injection / perfusion destinés à être utilisé dans les procédures médicales.

Manufacturer details

EUDAMED SRN
FR-PR-000004621

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Properties

Other properties (1)

  • Sterile: No