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Geo Scanbody

EUDAMED

Class I (EU MDR)

Ref 305Model SC-ITRWRef 2101Model OS-BH30Ref 803Model SC-ACR

by GeoMedi Co., Ltd.

Identity

Device Name
Geo Scanbody EUDAMED
Model / Reference
SC-ITRW EUDAMED
305 EUDAMED
OS-BH30 EUDAMED
2101 EUDAMED
SC-ACR EUDAMED
803 EUDAMED

Identifiers

Primary DI / UDI-DI
08800028710521 EUDAMED
08800028710422 EUDAMED
08800028710545 EUDAMED
Basic UDI-DI
B-08800028710521 EUDAMED
B-08800028710422 EUDAMED
B-08800028710545 EUDAMED
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Geo Scanbody by GeoMedi Co., Ltd. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
GeoMedi Co., Ltd.
EUDAMED SRN
KR-MF-000008801
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (3)

  • EUDAMED 045ec1df-a3da-42f9-84ed-29cb9dcb35cf 61 fields · synced Jul 20, 2026
  • EUDAMED 47c6093d-4c8b-4c00-819f-57c9eecfda84 61 fields · synced May 16, 2026
  • EUDAMED 84684063-cf1d-4591-860d-7750d1348d04 61 fields · synced May 18, 2026