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ReconWell

EUDAMED

Class IIa (EU MDR)

Ref 4260676710344Model ReconWell Dashboard, ReconWell AppRef 4260676710375

by be-on-market GmbH

Identity

Device Name
ReconWell EUDAMED
Model / Reference
ReconWell Dashboard, ReconWell App EUDAMED
4260676710344 EUDAMED
4260676710375 EUDAMED

Identifiers

Primary DI / UDI-DI
04260676710344 EUDAMED
04260676710375 EUDAMED
Basic UDI-DI
426067671_Reconwellone_TF EUDAMED
Direct Marketing DI
04260676710344 EUDAMED
04260676710375 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

ReconWell 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 (2)

  • EUDAMED 52b7558f-f947-4742-9482-9a5cd4cbab20 61 fields · synced Jul 21, 2026
  • EUDAMED e49475f3-d894-4a79-a7be-02c60803b24f 61 fields · synced May 17, 2026