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ActiMaris® SENSITIV – Wundspüllösung

by ActiMaris AG EUDAMED

Active European Union

Ref 30305Model ActiMaris® SENSITIVE Wound Irrigation Solution

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07649989411686 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  • Withdrawn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

Device Name
ActiMaris SENSITIVE
Model / Reference
ActiMaris® SENSITIVE Wound Irrigation Solution, 30305
Primary DI / UDI-DI
07649989411686
Basic UDI-DI
B-07649989411686
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® SENSITIV Wundspüllösung

Other devices from ActiMaris AG

See all devices from ActiMaris AG →

Properties

Show properties
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