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Rhiniclean

by Laboratoire CEVIDRA 2 variants

Ref ART00156

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3664831DM01RHINICLEAN93 Basic UDI-DI 03664831000133UDI-DIDate19 May 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
RHINICLEAN®,Sels pour irrigation nasale 30 sachets
Model / Reference
ART00156
Primary DI / UDI-DI
03664831000133
Basic UDI-DI
3664831DM01RHINICLEAN93
Direct Marketing DI
03664831000133
EMDN Code
Q030103 Nasal irrigation solutions
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000011081

Other devices from Laboratoire CEVIDRA

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