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Temporary implant base + screw

by Global D EUDAMED

Active European Union

Ref DEVCIR6.5H3Model In-Kone® pre-milled blanks/In-Kone® temporary titanium bases/In-Kone® titanium bases/In-Kone® TiBases

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3662601DPPIK006aaJ5 Basic UDI-DIDate22 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 00114-A Issued

    Quality management system EU MDR

    Notified body
    KIWA CERMET ITALIA S.P.A. 0476
    Issued
    24 Apr 2026
    Expires
    2 Dec 2030

Specification

EUDAMED

Device Name
In-Kone® Digital Solutions (Titanium – Non sterile)
Model / Reference
In-Kone® pre-milled blanks/In-Kone® temporary titanium bases/In-Kone® titanium bases/In-Kone® TiBases, DEVCIR6.5H3
Primary DI / UDI-DI
03662601073066
Basic UDI-DI
3662601DPPIK006aaJ5
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class IIb
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000024267

Other devices from Global D

See all devices from Global D →

Properties

  • Implantable
  • Sutures

Other properties (12)

  • Sterile: No
  • Reusable: No
  • Contains Latex: 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