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SAUER-Hautkleber - 10% Harz, auf Latexbasis, enthält Lanolin, Zinkoxid, 10% Harz, Flasche, 45 ml

by Manfred Sauer GmbH Germany EUDAMED

Ref 50.23

EMDN U0780

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42502745000015EK Basic UDI-DIDate2 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
SAUER Hautkleber
Model / Reference
50.23
Primary DI / UDI-DI
04250274505077
Basic UDI-DI
42502745000015EK
EMDN Code
U0780 Devices for the treatment of incontinence - accessories
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006287

Other devices from Manfred Sauer GmbH

See all devices from Manfred Sauer GmbH →

Properties & raw data

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

Sources (1)

  • EUDAMED ca3017aa-55fe-4213-808d-062bc54493ec 61 fields · synced 22 Oct 2026