← Back to catalogue

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
07613365500349 EUDAMED
07613365500318 EUDAMED
07613365500295 EUDAMED
Basic UDI-DI
7613365PWCBD2Y EUDAMED
Direct Marketing DI
07613365500349 EUDAMED
07613365500318 EUDAMED
07613365500295 EUDAMED
EMDN Code
Z12159003 DIFFUSION ANALYSIS EQUIPMENT EUDAMED
Z12159007 BODY PLETHYSMOGRAPHS 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000006566

Sources (3)

  • EUDAMED c6838244-5b57-48fc-8b44-82bb28f88065 61 fields · synced Jul 21, 2026
  • EUDAMED c8dd1d5c-e0af-4cd1-89f9-770724d35c91 61 fields · synced Jul 19, 2026
  • EUDAMED 1ba2b01b-7825-4f77-a7dd-25dbd0939326 61 fields · synced Jul 21, 2026