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Scanbody

EUDAMED

Class I (EU MDR)

Ref NOB_AC.R.SB

by Euroteknika

Identity

Device Name
Scanbody EUDAMED
Model / Reference
NOB_AC.R.SB EUDAMED

Identifiers

Primary DI / UDI-DI
03700977503708 EUDAMED
Basic UDI-DI
37009775scanbody3Z EUDAMED
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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 Euroteknika — 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
Euroteknika
EUDAMED SRN
FR-MF-000004032

Sources (1)

  • EUDAMED dac6db50-3ce1-42c3-b427-c9eae8aa9d2e 61 fields · synced Jun 18, 2026