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Lux P

EUDAMED

Class I (EU MDR)

Ref LUX-P

by PROMA REHA, s.r.o.

Identity

Trade Name
LUX P EUDAMED
Device Name
Mattress EUDAMED
Model / Reference
LUX-P EUDAMED

Identifiers

Primary DI / UDI-DI
85942023200702 EUDAMED
Basic UDI-DI
859420232M01KD EUDAMED
Direct Marketing DI
85942023200702 EUDAMED
EMDN Code
V080702 NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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

Lux P by PROMA REHA, s.r.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
PROMA REHA, s.r.o.
EUDAMED SRN
CZ-MF-000013860

Sources (1)

  • EUDAMED add0ad1d-58e7-41d9-9634-770eb9b1dded 61 fields · synced Jul 22, 2026