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Rinofluimucil Allergia

by bitop medical GmbH EUDAMED

Active European Union

Ref 38244/ANS03Model ANS02/ANS03/ANS07

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426252692ANS3K7N Basic UDI-DIDate13 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
medEctoin® Allergy Nasal Spray 1% / medEctoin® Allergy Nasal Spray 2% / medEctoin® Allergy Nasal Spray Forte
Model / Reference
ANS02/ANS03/ANS07, 38244/ANS03
Primary DI / UDI-DI
04262526920262
Basic UDI-DI
426252692ANS3K7N
Direct Marketing DI
04262526920262
EMDN Code
Q0399 ENT devices - other
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
DE-MF-000047028

Other devices from bitop medical GmbH

See all devices from bitop medical GmbH →

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