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Paranix Express Sprej + Hrebeň

by Omega Pharma International NV

Ref CT32088

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5400951PAREXPLOTIONCZ7 Basic UDI-DI 05400951005232UDI-DIDate28 May 2026RegisteredStatusActive

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  • Withdrawn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
Paranix Express Lotion
Model / Reference
CT32088
Primary DI / UDI-DI
05400951005232
Basic UDI-DI
5400951PAREXPLOTIONCZ7
EMDN Code
V901001 Lice elimination mechanical devices
Device Class
Class I
Medical Purpose
Treatment of head lice (Pediculosis capitis) and nits.

Manufacturer details

EUDAMED SRN
BE-PR-000007211

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Properties

Other properties (1)

  • Sterile: No