Skip to content

Rinaxan

by PHARMA LINE Srl

Ref PEESVISC0001Model 30 mL BOTTLE (sales size)

Rinaxan (PEESVISC0001) is a Class IIa device made by PHARMA LINE Srl, registered in EUDAMED on 28 May 2026 (Basic UDI-DI 805826596FT004MDRRC), active as of 24 Oct 2026.

Active European Union

CE MDR

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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805826596FT004MDRRC Basic UDI-DI 08058265962412UDI-DIDate28 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Viscoflu Spray Nasale
Model / reference
30 mL BOTTLE (sales size), PEESVISC0001
Primary DI / UDI-DI
08058265962412
Basic UDI-DI
805826596FT004MDRRC
EMDN code
R9099 Respiratory and anaesthesia devices - other
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
IT-MF-000032122

Similar devices in this category

Other devices filed under RESPIRATORY AND ANAESTHESIA DEVICES - OTHER.

Other devices from PHARMA LINE Srl

See all devices from PHARMA LINE Srl →

Properties

Other properties (14, all answered No)