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Bepanthen Sensiderm Cream

by Bayer Consumer Care AG Switzerland EUDAMED

Ref 1610821Model Bepanthen Itch Relief EMDN V9099

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-CH-MF-000014141H9 Basic UDI-DIDate16 Mar 2022RegisteredStatusActive

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  • Withdrawn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 22 Oct 2026

Device Name
Bepanthen Itch Relief
Model / Reference
Bepanthen Itch Relief, 1610821
Primary DI / UDI-DI
D-CH-MF-000014141H9
Basic UDI-DI
B-CH-MF-000014141H9
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000014141
Authorised representative
Bayer Vital GmbH DE-AR-000006698

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Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Implantable: No
  • 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 e372b23a-8fae-4691-8bc0-fde1578713e0 61 fields · synced 22 Oct 2026