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Consolor Ltd

United Kingdom (ex Northern Ireland) GB-MF-000008877 Last updated 23 May 2026

Devices
82
Registries
EUDAMED
FDA recalls
0

Catalogue82

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Showing 51-82 of 82

Authorised representatives

What Consolor Ltd makes

Consolor Ltd manufactures adjustable and fixed-position headrests for medical use, including designs with swan-neck or straight vertical tubes, ball joint mounting assemblies, and customizable covers. Their portfolio also includes pelvic belts, such as anti-rotational and dual-pull 2-point designs, featuring metal buckles and padded interfaces for patient stabilization.

All listed devices fall under Class I classification in the EU, and they are registered in the EUDAMED database. The company operates from the United Kingdom, adhering to regulatory requirements for medical devices within the European market.

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 Consolor Ltd manufacture?

Consolor Ltd specializes in adjustable and fixed-position headrests designed for medical use. Their products include headrests with various mounting assemblies like swan-neck or straight vertical tubes, ball joints, and customizable covers. Additionally, they produce pelvic belts, such as anti-rotational and dual-pull 2-point designs, which incorporate padded interfaces and metal buckles to aid in patient stabilization.

Where is Consolor Ltd based, and what regulatory market does it serve?

Consolor Ltd is based in the United Kingdom and operates within the European medical device market. Their devices are registered in the EUDAMED database, which is the official European Union registry for medical devices, ensuring compliance with EU regulatory requirements.

How are the devices manufactured by Consolor Ltd classified under EU regulations?

All devices manufactured by Consolor Ltd fall under Class I classification in the EU. This classification applies to low-risk medical devices, such as headrests and pelvic belts, which pose minimal risk to patients when used as intended. The classification is determined by factors like the device’s purpose, design, and potential risks, as outlined in EU Medical Device Regulations (MDR).

Are Consolor Ltd’s devices listed in any official regulatory databases?

Yes, Consolor Ltd’s devices are registered in EUDAMED, the European Union’s official database for medical devices. This registry ensures transparency and compliance with EU regulatory requirements, allowing healthcare professionals, authorities, and other stakeholders to verify the manufacturer’s details and device information.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
Nutsey Lane, Calmore Industrial Park, Southampton, United Kingdom (ex Northern Ireland)
Phone
+44 1202 827650
PRRC contact
Kieran Cheer
EUDAMED SRN
GB-MF-000008877