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Scanbody

EUDAMED

Class I (EU MDR)

Ref ASSB

by Snucone Co., Ltd.

Identity

Trade Name
Scanbody EUDAMED
Device Name
Scanbody EUDAMED
Model / Reference
ASSB EUDAMED

Identifiers

Primary DI / UDI-DI
08800020811813 EUDAMED
Basic UDI-DI
B-08800020811813 EUDAMED
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Scanbody by SNUCONE 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
Snucone Co., Ltd.
EUDAMED SRN
KR-MF-000036358
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 24353a87-e1c1-4ad1-b4a0-b7eac9604647 61 fields · synced Jun 20, 2026