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MEDORA Pro

EUDAMED

Class I (EU MDR)

Ref M4ST8520S0M011600T00T13C20

by Reha-Bed Sp. z o.o.

Identity

Trade Name
MEDORA Pro EUDAMED
Device Name
MEDORA EUDAMED
Model / Reference
M4ST8520S0M011600T00T13C20 EUDAMED

Identifiers

Primary DI / UDI-DI
05904183219523 EUDAMED
Basic UDI-DI
59041832MEDORAKG EUDAMED
Direct Marketing DI
05904183219523 EUDAMED
EMDN Code
V08060101 HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Category: Basic electric hospital bed

MEDORA Pro by Reha-Bed Sp. z o.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Basic electric hospital bed.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Reha-Bed Sp. z o.o.
EUDAMED SRN
PL-MF-000040289

Sources (1)

  • EUDAMED 13506055-ddc2-4e4e-b66e-ab4914f3bd83 61 fields · synced Jul 15, 2026