Skip to content

Two-Lumen Hemodialysis Catheter for High Volume Infusions

by Arrow International LLC (Subsidiary of Teleflex Incorporated) 7 variants

Ref KN-15122-F

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08019020000000000000046KG Basic UDI-DI 10801902190106UDI-DIDate20 May 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  • Withdrawn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

Specification

EUDAMED

Device Name
AHDC Procedure Pack
Model / Reference
KN-15122-F
Primary DI / UDI-DI
10801902190106
Basic UDI-DI
08019020000000000000046KG
EMDN Code
C01020202 Central venous double-lumen catheters, non-tunneled
Device Class
Class III
Medical Purpose
The large-bore two-lumen catheter permits venous access to the central circulation for temporary or short-term hemodialysis and apheresis. It may be inserted in the jugular subclavian or femoral veins.

Manufacturer details

EUDAMED SRN
US-PR-000023158

Related devices

Category: Central venous catheterization kit, short-term

Other devices from Arrow International LLC (Subsidiary of Teleflex Incorporated)

See all devices from Arrow International LLC (Subsidiary of Teleflex Incorporated) →

Properties

  • Sterile