Skip to content

Set de fistule branchement et débranchement N°75

by Raffin Medical 2 variants

Ref 400353-1

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3666002PP-ABO-K5 Basic UDI-DI 03700433512343UDI-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  • Withdrawn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
400353-1
Primary DI / UDI-DI
03700433512343
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