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Phoenix Basic Insertion Kit

by GMI Dental Implantology, S.L. 9 variants

Ref KYC0F0019Model KYC0F0003

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

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 08436610701587UDI-DIDate23 May 2022RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name
Phoenix Basic Insertion Kit
Model / Reference
KYC0F0003, KYC0F0019
Primary DI / UDI-DI
08436610701587
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