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Aquilea Respira Rinoget

by Ste Pharmaceuticals, S.L.U EUDAMED

Active European Union

Ref PL0116

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number843654262PL01168S Basic UDI-DIDate28 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Trade Name
Aquilea Respira Rinoget
Aquilea Respira
Device Name
Hypertonic Saline Solution Nasal Spray with Natural Essences
Model / Reference
PL0116
Primary DI / UDI-DI
08429603000606, 08429603000590
Market of Registration
Italy
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000000144

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