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DKutting LL Peripheral Scoring Balloon Dilatation Catheter

by DK Medical Technology Co., Ltd. EUDAMED

Active European Union

Ref DKL18-60120D

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6923533815DKLCL Basic UDI-DIDate26 Jun 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Peripheral Scoring Balloon Dilatation Catheter
Model / Reference
DKL18-60120D
Primary DI / UDI-DI
06923533802719
Basic UDI-DI
6923533815DKLCL
EMDN Code
C010402020199 PTA dilatation catheters - other
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000011218
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from DK Medical Technology Co., Ltd.

See all devices from DK Medical Technology Co., Ltd. →

Properties

Show properties
  • Sterile
Other properties (12)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No