Skip to content

ActiMaris® Wundgel

by ActiMaris AG Switzerland EUDAMED

Ref 30250Model ActiMaris® Wound Gel EMDN M04040102

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07649989411402 Basic UDI-DIDate21 Aug 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  • Withdrawn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
ActiMaris Wound Gel
Model / Reference
ActiMaris® Wound Gel, 30250
Primary DI / UDI-DI
07649989411402
Basic UDI-DI
B-07649989411402
EMDN Code
M04040102 Saline dressings in combination with other substances
Device Class
Class IIb
Market of Registration
Croatia

Manufacturer details

EUDAMED SRN
CH-MF-000035551
Authorised representative
Adriatic Health Factory d.o.o. HR-AR-000029035

From the manufacturer

Manufacturer's product page: ActiMaris® Wundgel

Other devices from ActiMaris AG

See all devices from ActiMaris AG →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • 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
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 07649989411402|B-07649989411402 61 fields · synced 24 Oct 2026