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ActiMaris® FORTE – Wundspüllösung

by ActiMaris AG Switzerland EUDAMED

Ref 30355Model ActiMaris® FORTE Wound Irrigation Solution EMDN M04040102

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07649989411679 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  • Withdrawn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 23 Oct 2026

Device Name
ActiMaris FORTE
Model / Reference
ActiMaris® FORTE Wound Irrigation Solution, 30355
Primary DI / UDI-DI
07649989411679
Basic UDI-DI
B-07649989411679
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® FORTE Wundspüllösung

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 95a58cfe-3b70-4d62-96ce-ab007f280bf5 61 fields · synced 23 Oct 2026