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Intraoral Scanbody

EUDAMED

Class I (EU MDR)

Ref OSHE532

by ARUM DENTISTRY Co., Ltd.

Identity

Trade Name
Intraoral Scanbody EUDAMED
Device Name
Intraoral Scanbody EUDAMED
Model / Reference
OSHE532 EUDAMED

Identifiers

Primary DI / UDI-DI
08809950316603 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

Category: Dental implant suprastructure, temporary, preformed, single-use

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

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

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 bbbb909d-b71e-4df1-8efb-3b6fb49b6fe2 61 fields · synced Jun 18, 2026