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BATEC MOBILITY

Spain ES-MF-000000576 Last updated 23 May 2026

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Devices
154
Registries
EUDAMEDGUDIDFDA
FDA recalls
0

Catalogue154

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Showing 1-50 of 154

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Batec Mobility Sl. US

What BATEC MOBILITY makes

Batec Mobility manufactures electric mobility devices, including manual and motorised wheelchairs and mobility scooters with varying speed limits (6 km/h, 10 km/h, or 15 km/h). Models include hemi (right-side) and quad configurations, as well as electric and rapid variants designed for indoor and outdoor use.

These devices fall under EU Class I medical devices and are registered in the EUDAMED database. The company is based in Spain.

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 Batec Mobility manufacture?

Batec Mobility specialises in electric mobility devices, including manual and motorised wheelchairs and mobility scooters. Their product range covers models with different speed limits (6 km/h, 10 km/h, or 15 km/h) and configurations such as hemi (right-side) and quad variants, as well as electric and rapid versions. These devices are designed for both indoor and outdoor use, catering to varying mobility needs.

Where is Batec Mobility based?

Batec Mobility is based in Spain. The company’s location in the European Union aligns with its compliance requirements for medical devices sold within the region.

Which regulatory registries list Batec Mobility’s devices?

Batec Mobility’s devices are listed in the EUDAMED database, which is the official European Union database for medical devices. This registry ensures transparency and traceability of devices authorised under EU regulations.

How are Batec Mobility’s devices classified under EU regulations?

Batec Mobility’s devices fall under EU Class I classification. This classification is typically assigned to low-risk medical devices, such as mobility aids, where the risk to patients is minimal. The classification determines the regulatory pathway and compliance requirements for these products.

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

Information

Country
Spain
Address
2, Illa de Buda, Sant Quirze del Vallès, Spain
Phone
+34935442003
PRRC contact
jordi clapes
EUDAMED SRN
ES-MF-000000576