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Adhe-FLOW® MONO Désilet kit cathéter d’hémodialyse fémorale mono lumière FR10 L.: 18cm

by Adhe-Els SA. 3 variants

Ref SLC-1018DK-CHModel Adhe-FLOW® kit cathéter d’hémodialyse fémorale

Active European Union

CE MDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-SLC-1018DK-CHG6 Basic UDI-DI D-SLC-1018DK-CHG6UDI-DIDate5 Apr 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
Adhe-FLOW® kit cathéter d’hémodialyse fémorale, SLC-1018DK-CH
Primary DI / UDI-DI
D-SLC-1018DK-CHG6
Basic UDI-DI
B-SLC-1018DK-CHG6
EMDN Code
F0303, F900299
Device Class
Class IIa
EU market of registration
France

Manufacturer details

EUDAMED SRN
TN-MF-000011757
Authorised representative
ADHE-ELS FRANCE FR-AR-000001654

Other devices from Adhe-Els SA.

See all devices from Adhe-Els SA. →

Properties

  • Sterile
  • Reprocessed

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No