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Fixierstrumpf für Beinbeutel

by Tytex a/S EUDAMED

Active European Union

Ref 05/02/11/OS/M/GHC

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number57039361265120AAGX Basic UDI-DIDate19 Oct 2026RegisteredStatusActive

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  • Withdrawn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
Urology
Model / Reference
05/02/11/OS/M/GHC
Primary DI / UDI-DI
05703936118355
Basic UDI-DI
57039361265120AAGX
EMDN Code
W05010280 Urine collection devices - accessories
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DK-MF-000003620

Other devices from Tytex a/S

See all devices from Tytex a/S →

Properties

Other properties (13)

  • Sterile: No
  • 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