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Planmed Clarity+

EUDAMED

Class IIb (EU MDR)

Ref 30063790Ref 20009418

by Planmed Oy

Identity

Device Name
Planmed Clarity+ EUDAMED
Planmed Clarity EUDAMED
Model / Reference
30063790 EUDAMED
20009418 EUDAMED

Identifiers

Primary DI / UDI-DI
06430035430147 EUDAMED
06430035430116 EUDAMED
Basic UDI-DI
6430035430055U EUDAMED
6430035430025N EUDAMED
EMDN Code
Z11030202 DIGITAL MAMMOGRAPHY SYSTEMS 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

Planmed Clarity+ by Planmed 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
Planmed Oy
EUDAMED SRN
FI-MF-000006837

Sources (2)

  • EUDAMED cb01509c-9b00-43fd-8f68-23f51b0d9973 61 fields · synced Jul 21, 2026
  • EUDAMED a41a4857-e006-4a7d-b5fb-5f584e516062 61 fields · synced Jul 20, 2026