Skip to content

Urs-R-10-120

by Allium Ltd. Israel EUDAMED

Ref 731-2120Model URS-R-10-120 EMDN U020399

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07290013096395 Basic UDI-DIDate18 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Ureteral Stent (URS)
Model / Reference
URS-R-10-120, 731-2120
Primary DI / UDI-DI
07290013096395
Basic UDI-DI
B-07290013096395
EMDN Code
U020399 Ureteral stents - other
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000009302
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Allium Ltd.

See all devices from Allium Ltd. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED c0d16d59-8982-47af-bdd1-bcc7fc44eb7b 61 fields · synced 24 Oct 2026