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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Mattress — 9 UDI-DI variants, MDR (PROMA REHA, s.r.o.)

MD Atlas
PROMA REHA, s.r.o.

Data from EUDAMED, last updated May 31, 2026

Mattress

859420232M01KD

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: PROMA REHA, s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859420232M01KD
Device name: Mattress
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: PROMA REHA, s.r.o.
SRN: CZ-MF-000013860
Country: Czechia
Email: viktor.kratochvil@promareha.cz
Phone: +420775776002

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSPXPAPFND5HWYW2GRG3C22T

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

LUX-P85942023200702
LUX-S85942023200566
Pasivní-matrace-TITAN-25085942023201006
Pasivni-matrace-TITAN-45085942023201174
Sendvic85942023200184
SOFT-FLEX85942023200252
VICTORIE85942023200870
VISCO-LUX85942023200320
VISCO-LUX-FLEX85942023200498