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KaVo ProXam 3DQ

EUDAMED

Class IIb (EU MDR)

Ref 30056789Ref 30038583

by Planmeca Oy

Identity

Trade Name
KaVo ProXam 3DQ EUDAMED
KaVo ProXam 3DQ Pro EUDAMED
Device Name
Planmeca ProMax 3D Plus EUDAMED
Planmeca ProMax 3D Mid EUDAMED
Model / Reference
30056789 EUDAMED
30038583 EUDAMED

Identifiers

Primary DI / UDI-DI
06430035421039 EUDAMED
06430035420957 EUDAMED
Basic UDI-DI
6430035420135L EUDAMED
6430035420125J EUDAMED
EMDN Code
Z11030380 INSTRUMENTS FOR EXTRAORAL DENTAL RADIOLOGY - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIb 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

KaVo ProXam 3DQ by Planmeca Oy — Class IIb — 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 (2)

  • EUDAMED 361f0717-c298-450d-a753-2b235a8d218d 61 fields · synced Jul 29, 2026
  • EUDAMED a1ac36ed-ee80-4e8b-ac2e-8151664a258c 61 fields · synced May 18, 2026