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Rinophar

by Demo S.A. Pharmaceutical Industry

Ref Rinophar

Rinophar is a Class IIb device made by Demo S.A. Pharmaceutical Industry, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI B-05205411014614), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05205411014614 Basic UDI-DI 05205411014614UDI-DIDate26 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Rinophar
Model / reference
Rinophar
Primary DI / UDI-DI
05205411014614
Basic UDI-DI
B-05205411014614
EMDN code
Q030103 Nasal irrigation solutions
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000023096

Similar devices in this category

Other devices filed under NASAL IRRIGATION SOLUTIONS.

Other devices from Demo S.A. Pharmaceutical Industry

Properties

  • Supplied sterile
Other properties (11, all answered No)