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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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xRover Reha — 8 UDI-DI variants, MDR (Volter s.r.o.)

MD Atlas
Volter s.r.o.

Data from EUDAMED, last updated May 30, 2026

xRover Reha

859421717500BUGGY8A

8 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: Volter s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859421717500BUGGY8A
Device name: xRover Reha
Device model: xRover Reha
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Volter s.r.o.
SRN: CZ-MF-000041158
Country: Czechia
Email: info@volter.cz
Phone: +420 222 962 237

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSFM0W95S8Y058G8V1DSN966

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

50300208594217170028
50300608594217170035
50300108594217170004
50200208594217170059
50200608594217170066
50200108594217170042
50100208594217170080
50100108594217170073