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Planmeca Pro50

EUDAMED

Class IIa (EU MDR)

Ref 30045357

by Planmeca Oy

Identity

Device Name
Planmeca Pro50 EUDAMED
Model / Reference
30045357 EUDAMED

Identifiers

Primary DI / UDI-DI
06430035421008 EUDAMED
Basic UDI-DI
6430035420225M EUDAMED
Direct Marketing DI
06430035421008 EUDAMED
EMDN Code
Z12110101 DENTAL TREATMENT UNITS EUDAMED

Classification

Device Class
Class IIa 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

Category: Dental delivery system

Planmeca Pro50 by Planmeca Oy — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system.

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 64d1e6d0-b987-403a-98b0-599be095c68e 61 fields · synced Aug 3, 2026