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Scanbody

EUDAMED

Class I (EU MDR)

Ref SMBL1901HModel Scanbody

by Heliocos GmbH

Identity

Device Name
Scanbody EUDAMED
Model / Reference
Scanbody EUDAMED
SMBL1901H EUDAMED

Identifiers

Primary DI / UDI-DI
04251923112059 EUDAMED
Basic UDI-DI
425192311931142154259K EUDAMED
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES 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

Scanbody by Heliocos GmbH — 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

Manufacturer
Heliocos GmbH
EUDAMED SRN
DE-MF-000006272

Sources (1)

  • EUDAMED 7b847b1c-d216-4f06-afe7-49873d573fd6 61 fields · synced Oct 5, 2026