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PowerCube+ Series

EUDAMED

Class IIa (EU MDR)

Ref 050000000Model PowerCube+ Series

by Ganshorn Medizin Electronic GmbH

Identity

Trade Name
PowerCube+ Series EUDAMED
Model / Reference
PowerCube+ Series EUDAMED
050000000 EUDAMED

Identifiers

Primary DI / UDI-DI
07613365500356 EUDAMED
Basic UDI-DI
7613365PWCBD2Y EUDAMED
Direct Marketing DI
07613365500356 EUDAMED
EMDN Code
Z12159003 DIFFUSION ANALYSIS EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

PowerCube+ Series by Ganshorn Medizin Electronic Gmbh — Class IIa — 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

EUDAMED SRN
DE-MF-000006566

Sources (1)

  • EUDAMED fd7f7911-8257-4676-b834-1e48284a1cdd 61 fields · synced May 23, 2026