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Hydromol Cremă

by Alliance Pharmaceuticals Limited United Kingdom EUDAMED

Ref 508182Model Hydromol Cream EMDN M9002

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-15036631011339 Basic UDI-DIDate2 Sep 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  • Withdrawn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
Hydromol Cream
Model / Reference
Hydromol Cream, 508182
Primary DI / UDI-DI
15036631011339
Basic UDI-DI
B-15036631011339
EMDN Code
M9002 Protective devices, lubricants and soothing devices (sprays, gels, fluids and creams)
Device Class
Class I
Market of Registration
Romania

Manufacturer details

EUDAMED SRN
GB-MF-000023165
Authorised representative
Alliance Pharma (Ireland) Ltd IE-AR-000022483

Other devices from Alliance Pharmaceuticals Limited

See all devices from Alliance Pharmaceuticals Limited →

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 e33b64ed-1f34-4ea0-9983-cce53a36a4da 61 fields · synced 24 Oct 2026