CamNtech devices are now listed on the EUDAMED Database.

EUDAMED will provide a living picture of the lifecycle of medical devices that are made available in the European Union (EU). It will integrate different electronic systems to collate and process information about medical devices and related companies (e.g. manufacturers). In doing so, EUDAMED aims to enhance overall transparency, including through better access to information for the public and healthcare professionals, and to enhance coordination between the different Member States in the EU.

Use of EUDAMED is currently voluntary until all database modules are completed and launched, however, forward thinking companies have already begun listing devices thus linking together the details of their Devices, EC-REP, EU Importers and Manufacturing facilities.

Regulatory compliance is essential for use of wearable technology in clinical trials and general clinical applications. CamNtech has a long-established Quality Management System and key Worldwide Regulatory Compliances.

The public EUDAMED database may be accessed here:



UK & International customers

CamNtech Ltd.
Manor Farm
PE28 9JD, UK

US customers

CamNtech Inc.
630 Boerne Stage Airfield,
Texas 78006,


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