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Remo-wax øredråber med sprøjte

by Orion Oyj 2 variants

Ref 100427

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number643210RPP001YT Basic UDI-DI 06432100001740UDI-DIDate26 Mar 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Remo-Wax
Model / Reference
100427
Primary DI / UDI-DI
06432100001740
Basic UDI-DI
643210RPP001YT
EMDN Code
Q030499 Otology devices - other
Device Class
Class IIa
Medical Purpose
Dissolve impacted ear wax

Manufacturer details

EUDAMED SRN
FI-PR-000001596

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Properties

Other properties (1)

  • Sterile: No