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Lynx

EUDAMED

Class I (EU MDR)

Ref LXSW9020S1L010100S00T06A06

by Reha-Bed Sp. z o.o.

Identity

Trade Name
LYNX EUDAMED
Device Name
LYNX EUDAMED
Model / Reference
LXSW9020S1L010100S00T06A06 EUDAMED

Identifiers

Primary DI / UDI-DI
05904183223872 EUDAMED
Basic UDI-DI
59041832LYNXTS EUDAMED
Direct Marketing DI
05904183223872 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

Lynx by Reha-Bed Sp. z o.o. — 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
Reha-Bed Sp. z o.o.
EUDAMED SRN
PL-MF-000040289

Sources (1)

  • EUDAMED ca05d806-e0d5-46b3-8bf5-3fbed4d6d76a 61 fields · synced Jun 18, 2026