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Phoenix - Rahmen standard

EUDAMED

Class I (EU MDR)

Ref 8500

by Berollka-aktiv Rollstuhltechnik GmbH

Identity

Trade Name
Phoenix - Rahmen standard EUDAMED
Device Name
Phoenix EUDAMED
Model / Reference
8500 EUDAMED

Identifiers

Primary DI / UDI-DI
04066358100102 EUDAMED
Basic UDI-DI
40663581020850000006R EUDAMED
Direct Marketing DI
04066358100102 EUDAMED
EMDN Code
Y122106 REAR SELF-PROPELLED WHEELCHAIRS EUDAMED

Classification

Device Class
Class I 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

Phoenix - Rahmen standard by Berollka-aktiv Rollstuhltechnik GmbH — Class I — 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-000007043

Sources (1)

  • EUDAMED 54da819f-a0db-41d3-b129-e11b694408fb 61 fields · synced Jun 18, 2026