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Planmeca Emerald S

EUDAMED

Class I (EU MDR)

Ref 30018474

by Planmeca Oy

Identity

Device Name
Planmeca Emerald S EUDAMED
Model / Reference
30018474 EUDAMED

Identifiers

Primary DI / UDI-DI
06430035420889 EUDAMED
Basic UDI-DI
6430035420205H 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 S 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 4922b01e-be2e-4efc-9e06-d3be1b2ff8f9 61 fields · synced May 22, 2026