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Otostick Baby

by Innovaciones Disras Sl 7 variants

Ref 8437010702655Model OTOSTICK (8 und.)

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 Number8437010702006XD Basic UDI-DI 08437010702655UDI-DIDate20 Mar 2023RegisteredStatusActive

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  • Withdrawn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
OTOSTICK, Corrector estético de orejas
Model / Reference
OTOSTICK (8 und.), 8437010702655
Primary DI / UDI-DI
08437010702655
Basic UDI-DI
8437010702006XD
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
ES-MF-000003854

Other devices from Innovaciones Disras Sl

See all devices from Innovaciones Disras Sl →

Properties

  • Contains Latex

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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