Skip to content

Grand Konisch™ Dental Implant 4.3D 18L

by Medigma Biomedical GmbH

Ref MGKI1843Model Konisch Implant

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-DEMF000009412MGKI1843YX Basic UDI-DI D-DEMF000009412MGKI1843YXUDI-DIDate19 Jun 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Konisch Implant
Model / Reference
Konisch Implant, MGKI1843
Primary DI / UDI-DI
D-DEMF000009412MGKI1843YX
Basic UDI-DI
B-DEMF000009412MGKI1843YX
EMDN Code
P01020101 Dental implants
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
DE-MF-000009412

Other devices from Medigma Biomedical GmbH

See all devices from Medigma Biomedical GmbH →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • 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