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Implant Protect Kit

by GMI Dental Implantology, S.L.

Ref KPA0F0001

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number843656274KPA02FJ Basic UDI-DI 08436610700412UDI-DIDate18 Sep 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  • Withdrawn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
Implant Protect Kit
Model / Reference
KPA0F0001
Primary DI / UDI-DI
08436610700412
Basic UDI-DI
843656274KPA02FJ
EMDN Code
Q0199 Odontology devices - other
Device Class
Class I
Medical Purpose
The device is intended for direct application to the surface of a dental implant affected by mucositis or periimplantitis, following non-surgical mechanical treatment. It is designed to create a protective coating on the implant surface, intended to reduce the recurrence of mucositis and periimplantitis following non-surgical mechanical treatment.

Manufacturer details

EUDAMED SRN
ES-PR-000024245

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Properties

Other properties (1)

  • Sterile: No