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Quixx® forte

by Aurena Laboratories AB Sweden EUDAMED

Ref 301477Model REF 2018

EMDN Q030103

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7332343200127J Basic UDI-DIDate19 Sep 2024RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Withdrawn
  • Not covered

European Union — CE/MDR Withdrawn

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Specification

EUDAMED · synced 25 Oct 2026

Device Name
Aurena Nasal Spray, Hypertonic
Model / Reference
REF 2018, 301477
Primary DI / UDI-DI
07332343300930
Basic UDI-DI
7332343200127J
Direct Marketing DI
07332343300930
EMDN Code
Q030103 Nasal irrigation solutions
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
SE-MF-000002890

Other devices from Aurena Laboratories AB

See all devices from Aurena Laboratories AB →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (12)
  • 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 07332343300930|7332343200127J 61 fields · synced 25 Oct 2026