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Intraoral Scanbody

EUDAMED

Class I (EU MDR)

Ref OSHE390P

by ARUM DENTISTRY Co., Ltd.

Identity

Trade Name
Intraoral Scanbody EUDAMED
Device Name
Intraoral Scanbody EUDAMED
Model / Reference
OSHE390P EUDAMED

Identifiers

Primary DI / UDI-DI
08809924587220 EUDAMED
Basic UDI-DI
88000557ISBXH EUDAMED
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Intraoral Scanbody by ARUM DENTISTRY Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
KR-MF-000009313
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (1)

  • EUDAMED 4a7492fc-02ca-4747-8a3a-716fdf9db18c 61 fields · synced Sep 17, 2026