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UROMED HEPARIUS Ureteral Stent

by UROMED Kurt Drews KG Germany EUDAMED

Ref 4166.24 EMDN U020302

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number04250098810055ET Basic UDI-DIDate3 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 20561GB450250724 Issued

    Technical documentation EU MDR

    Notified body
    Notified body 0482
    Issued
    24 Jul 2025
    Expires
    23 Jul 2030

Specification

EUDAMED · synced 25 Oct 2026

Device Name
US01
Model / Reference
4166.24
Primary DI / UDI-DI
04250098841573
Basic UDI-DI
04250098810055ET
EMDN Code
U020302 Double loop ureteral stents
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006084

Other devices from UROMED Kurt Drews KG

See all devices from UROMED Kurt Drews KG →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (12)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Sutures: 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

Sources (1)

  • EUDAMED 04250098841573|04250098810055ET 61 fields · synced 25 Oct 2026