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Slade AR

EUDAMED

Class I (EU MDR)

Ref 505

by Berollka-aktiv Rollstuhltechnik GmbH

Identity

Trade Name
Slade AR EUDAMED
Device Name
Slade EUDAMED
Model / Reference
505 EUDAMED

Identifiers

Primary DI / UDI-DI
04066358100065 EUDAMED
Basic UDI-DI
40663581020405000003R EUDAMED
Direct Marketing DI
04066358100065 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

Slade AR 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 1116ae47-e0f4-4223-ac74-f320c5ad2eb0 61 fields · synced Jun 19, 2026