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Phoenix Basic Insertion Kit

by GMI Dental Implantology, S.L. 9 variants

Ref KYC0F0021Model KYC0F0003

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 Number843656274KYCIBLZ Basic UDI-DI 08436610705769UDI-DIDate23 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  • Withdrawn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
Phoenix Basic Insertion Kit
Model / Reference
KYC0F0003, KYC0F0021
Primary DI / UDI-DI
08436610705769
Basic UDI-DI
843656274KYCIBLZ
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
Aid in the the surgical placement of dental implants in upper or lower jaw to provide a support for prosthetic devices such as artificial teeth, in order to restore the patient’s masticatory function or poor aesthetics.

Manufacturer details

EUDAMED SRN
ES-PR-000024245

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Properties

Other properties (1)

  • Sterile: No