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ActiMaris® NASAL Spray

by ActiMaris AG Switzerland EUDAMED

Ref 33020Model ActiMaris® NASAL Spray EMDN Q030199

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07649989411013 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  • Withdrawn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 NASAL
Model / Reference
ActiMaris® NASAL Spray, 33020
Primary DI / UDI-DI
07649989411013
Basic UDI-DI
B-07649989411013
EMDN Code
Q030199 Nasopharyngeal devices - other
Device Class
Class I
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® NASAL Spray

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 07649989411013|B-07649989411013 61 fields · synced 24 Oct 2026