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Analog

EUDAMED

Class I (EU MDR)

Ref ALA_H42

by Euroteknika

Identity

Device Name
Analog EUDAMED
Model / Reference
ALA_H42 EUDAMED

Identifiers

Primary DI / UDI-DI
03700977509953 EUDAMED
Basic UDI-DI
37009775analogueYB EUDAMED
EMDN Code
Q010280 PROSTHETIC DENTISTRY DEVICES - ACCESSORIES 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

Analog 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 9bd71885-e511-4b3f-9ac2-2fc784c6a990 61 fields · synced Aug 3, 2026