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WundFit

EUDAMED

Class IIa (EU MDR)

Ref 04260676710351

by be-on-market GmbH

Identity

Device Name
WundFit EUDAMED
Model / Reference
04260676710351 EUDAMED

Identifiers

Primary DI / UDI-DI
04260676710351 EUDAMED
Basic UDI-DI
426067671_Wundfit_TA EUDAMED
Direct Marketing DI
04260676710351 EUDAMED
EMDN Code
Z129092 VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - MEDICAL DEVICE SOFTWARE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

WundFit by be-on-market 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

Manufacturer
be-on-market GmbH
EUDAMED SRN
DE-MF-000006151

Sources (1)

  • EUDAMED 7a8442e9-442a-48d9-ae89-d831734f8af1 61 fields · synced Aug 1, 2026