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Bepanthen® Sensiderm Cremă

by Bayer Consumer Care AG EUDAMED

Active European Union

Ref 04064273120113

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberG70 054972 0038 Date23 Jun 2025IssuedStatusActive expires 17 Feb 2030

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  • Withdrawn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)

Specification

EUDAMED

Device Name
Bepanthen Itch Relief Cream
Model / Reference
04064273120113
Primary DI / UDI-DI
04064273120113
Basic UDI-DI
4064273B161082100G5
EMDN Code
M04041503 Dressings in solutions, emulsions, gels, powders with synthetic components
Device Class
Class III
Market of Registration
France

Manufacturer details

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

Other devices from Bayer Consumer Care AG

See all devices from Bayer Consumer Care AG →

Properties

Show properties
  • Incorporates Medicinal Product
Other properties (12)
  • 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