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Planmeca Emerald

EUDAMED

Class I (EU MDR)

Ref 30006359

by Planmeca Oy

Identity

Device Name
Planmeca Emerald EUDAMED
Model / Reference
30006359 EUDAMED

Identifiers

Primary DI / UDI-DI
06430035420568 EUDAMED
Basic UDI-DI
6430035420035H EUDAMED
EMDN Code
Z110601 LASER IMAGING SCANNER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

Planmeca Emerald by Planmeca Oy — 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
Planmeca Oy
EUDAMED SRN
FI-MF-000006499

Sources (1)

  • EUDAMED bce25cc9-d511-4d7d-9d73-466981dd8331 61 fields · synced Jul 11, 2026