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UDI Compass
Unknown / Not in EUDAMED

Snapshot 2026-10-19 · Link to EUDAMED

Planmeca Pro50

UDI-DI 06430035421008Basic UDI-DI 6430035420225M

Class IIa · MDR · Planmeca Oy

Identification
Model
—
Issuing agency
GS1
Device status
active
Sterile
No
Implantable
No
Measuring function
No
Reusable surgical
No
Certificates

FI23/00000059

EU quality management system · unknown

Notified body: SGS FIMKO OY (0598)

Valid from 2025-09-17 · Expiry 2030-06-26

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

Planmeca Oy

SRN FI-MF-000006499

FI · Helsinki

manufacturer

Related UDI-DIs

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/planmeca-pro50-1008 · UDI page: /udi/06430035421008

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