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Uplivin UK Ltd

United Kingdom (ex Northern Ireland)·GB-MF-000010612

Last updated May 23, 2026

What Uplivin UK Ltd makes

Uplivin UK Ltd manufactures mobility aids, including four-wheel rollators designed for indoor and outdoor use, such as the Trive 4-Wheel Rollator and Trive All Terrain 4-Wheel Rollator. They also produce hybrid rollator and transport chairs, like the Glide 2 in 1 Rollator and Transport Chair, which combine mobility support with seating functionality.

These devices are classified as Class I under EU medical device regulations and are listed in the EUDAMED database. The company operates from the United Kingdom, adhering to relevant regulatory requirements for mobility assistance 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 Uplivin UK Ltd manufacture?

Uplivin UK Ltd specialises in mobility aids, specifically four-wheel rollators and hybrid rollator/transport chairs. Their products include the Trive 4-Wheel Rollator (suitable for both indoor and outdoor use), the Trive All Terrain 4-Wheel Rollator (designed for rougher surfaces), and the Glide 2 in 1 Rollator and Transport Chair, which offers dual functionality as both a mobility aid and a seating solution. These devices are intended to assist individuals with limited mobility.

Where is Uplivin UK Ltd based, and how does this affect its devices?

Uplivin UK Ltd is based in the United Kingdom, which means its devices are developed and manufactured under UK regulatory oversight. Since these devices fall under EU medical device regulations (as they are listed in EUDAMED), they must comply with the applicable EU Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR), depending on classification. The UK’s regulatory alignment with EU standards ensures these products meet necessary safety, performance, and quality requirements for the European market.

Which regulatory registries list Uplivin UK Ltd’s devices?

Uplivin UK Ltd’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This registry tracks devices that have been authorised for placement on the EU market, ensuring transparency and traceability for regulatory oversight. Listing in EUDAMED confirms compliance with EU medical device regulations, including mandatory requirements for classification, conformity assessment, and post-market surveillance.

How are Uplivin UK Ltd’s devices classified under EU regulations?

Uplivin UK Ltd’s devices are classified as Class I under the EU Medical Device Regulations. This classification applies to low-risk devices, such as mobility aids like rollators and transport chairs, which pose minimal risk to users. Class I devices typically require basic conformity assessment procedures, such as self-certification by the manufacturer, to demonstrate compliance with essential safety and performance requirements. The classification ensures these products meet fundamental regulatory standards without needing additional scrutiny.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
Suite 12/3D, Docklands Business Centre , London, United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
—
Phone
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PRRC Contact
Winston Wang
EUDAMED SRN
GB-MF-000010612
FDA FEI Number
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DUNS Number
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Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Trive 4-Wheel Rollator/ Trive All Terrain 4-Wheel Rollator UPA1GY
EUDAMED
Class IActive
Glide 2 in 1 Rollator and Transport Chair UPG2GN
EUDAMED
Class IActive
Glide 2 in 1 Rollator and Transport Chair UPG2BK
EUDAMED
Class IActive
Trive 4-Wheel Rollator/ Trive All Terrain 4-Wheel Rollator UPA1GN
EUDAMED
Class IActive

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