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Luna C Duo Lux

EUDAMED

Class I (EU MDR)

Ref SFK/LN/D/LUX/CC/25

by Reha-Bed Sp. z o.o.

Identity

Trade Name
LUNA C DUO LUX EUDAMED
Device Name
Luna EUDAMED
Model / Reference
SFK/LN/D/LUX/CC/25 EUDAMED

Identifiers

Primary DI / UDI-DI
05904183224398 EUDAMED
Basic UDI-DI
59041832LUNARQ EUDAMED
Direct Marketing DI
05904183224398 EUDAMED
EMDN Code
V0499 CLINICAL USE CONTAINERS (NON-IVD) - OTHER 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: Instrument transport trolley system

Luna C Duo Lux by Reha-Bed Sp. z o.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Instrument transport trolley system.

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 dc663226-7c57-486e-9e3c-6093fd5ca92a 61 fields · synced Aug 1, 2026