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Set de cathéter débranchement N°31

by Raffin Medical 2 variants

Ref 400368-1

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3666002PP-ABO-K5 Basic UDI-DI 03700433512381UDI-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  • Withdrawn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
400368-1
Primary DI / UDI-DI
03700433512381
Basic UDI-DI
3666002PP-ABO-K5
EMDN Code
F0303 Haemodialysis kits
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

Other devices from Raffin Medical

See all devices from Raffin Medical →

Properties

Other properties (1)

  • Sterile: No