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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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Kinetic bed — 12 UDI-DI variants, MDR (PROMA REHA, s.r.o.)

MD Atlas
PROMA REHA, s.r.o.

Data from EUDAMED, last updated May 31, 2026

Kinetic bed

859420232LS01F6

12 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

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 859420232LS01F6
Device name: Kinetic bed
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSHTKNMZJ34CX8F53B23C13T

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

HESTIA-3C85942023201792
HESTIA-2C85942023201624
INVENT-2C85942023201242
INVENT-2C85942023201310
INVENT-PRO-2C85942023201488
INVENT-PRO-3C85942023201556
TITAN-10085942023204908
TITAN-12085942023205066
TITAN-PRO-10008594202320513
TITAN-PRO-12085942023205202
VISTA85942023202478
VISTA-PRO85942023207800