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X5

EUDAMED

Class I (EU MDR)

Ref X5

by Sotec Medical

Identity

Device Name
X5 EUDAMED
Model / Reference
X5 EUDAMED

Identifiers

Primary DI / UDI-DI
37603459614480 EUDAMED
Basic UDI-DI
376034596FLX5EJ EUDAMED
Direct Marketing DI
37603459614480 EUDAMED
EMDN Code
V08060101 HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

X5 by Sotec Medical — 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

Manufacturer
Sotec Medical
EUDAMED SRN
FR-MF-000028950

Sources (1)

  • EUDAMED 77fe1623-5b12-418b-9c9b-fb0eed3c69ce 61 fields · synced Jun 18, 2026