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Scanbody

EUDAMED

Class I (EU MDR)

Ref ETK_NA.4XSB

by Euroteknika

Identity

Device Name
Scanbody EUDAMED
Model / Reference
ETK_NA.4XSB EUDAMED

Identifiers

Primary DI / UDI-DI
03700977506563 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

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

Scanbody by Euroteknika — 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

Manufacturer
Euroteknika
EUDAMED SRN
FR-MF-000004032

Sources (1)

  • EUDAMED f8c6417d-8426-42d5-a424-f06f92c8b5eb 61 fields · synced Jun 18, 2026