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Volter s.r.o.

Czechia CZ-MF-000041158 Last updated 17 Sep 2026

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Devices
82
Registries
EUDAMED
FDA recalls
0

Catalogue82

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About

Innovative wheelchair for active life. Certified, light and safe. Made in Czech Republic.

Translated from the manufacturer's own website. Source

What Volter s.r.o. makes

Volter s.r.o. manufactures a range of medical devices designed for pediatric and infant use, including seating systems like the Cykloset (Models 26” and 29”), adjustable footrests, and ergonomic supports such as back cushions and low-positioned seats. The portfolio also includes mobility aids like ski sets, hand brakes, and transport bags, as well as wheeled accessories such as jogging sets with metal wheels and standard or low-profile footrests. These devices are tailored for children’s physical therapy and assistive mobility needs.

All listed devices fall under Class I classification under EU medical device regulations and are registered in the euDAMED database. The company operates from the Czech Republic, adhering to EU regulatory requirements for non-active Class I products.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Volter s.r.o. manufacture?

Volter s.r.o. specializes in medical devices primarily designed for pediatric and infant use. Their portfolio includes seating systems like the Cykloset (Models 26” and 29”), ergonomic supports such as back cushions and low-positioned seats, mobility aids like ski sets and hand brakes, and wheeled accessories including jogging sets with metal wheels and transport bags. These devices are tailored to assistive mobility and physical therapy needs for children.

Where is Volter s.r.o. based, and how does this affect its regulatory compliance?

Volter s.r.o. is based in the Czech Republic, which is part of the European Union. Since their devices fall under Class I classification, they must comply with EU medical device regulations. Being based in the EU allows them to directly register their devices in the euDAMED database, ensuring transparency and adherence to EU regulatory requirements for non-active Class I products.

Which regulatory registries list Volter s.r.o.’s medical devices?

Volter s.r.o.’s medical devices are listed in the euDAMED database, which is the official EU registry for medical devices. This registry is maintained under EU medical device regulations to ensure traceability and compliance for Class I devices, including those manufactured by Volter.

How are Volter s.r.o.’s devices classified under EU regulations?

All of Volter s.r.o.’s listed devices fall under Class I classification according to EU medical device regulations. This classification applies to low-risk devices, such as seating systems, ergonomic supports, and mobility aids for pediatric use, which typically do not require invasive procedures or active medical functions. The classification ensures appropriate regulatory oversight while streamlining compliance for non-active devices.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Czechia
Address
1216/46, Klimentská , Prague, Czechia
Website
www.xrover.cz
Phone
+420 222 962 237
PRRC contact
Jiri Vavra
EUDAMED SRN
CZ-MF-000041158