Skip to content

Mediforte Wundgel 60ml

by CF Pharma Ireland Ltd Ireland EUDAMED

Ref FP1929Model Mediforte Wound Hydrogel 60ml German EMDN V9099

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05391525739335 Basic UDI-DIDate13 Nov 2024RegisteredStatusActive

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  • Withdrawn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
Mediforte Wundgel 60ml German
Model / Reference
Mediforte Wound Hydrogel 60ml German, FP1929
Primary DI / UDI-DI
05391525739335
Basic UDI-DI
B-05391525739335
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IE-MF-000004595

Related devices

Category: Device sterilization/disinfection container, reusable

Other devices from CF Pharma Ireland Ltd

See all devices from CF Pharma Ireland Ltd →

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 ec2bbaab-b72f-4944-b6a1-1ee3ef2547f3 61 fields · synced 22 Oct 2026