Natec Medical Limited is committed to providing high quality Medical Devices, that would meet or exceed the expectations of our customers by;

Understanding the requirements and meeting the needs of our customers and patients,

Involving all employees in the delivery of quality products,

Maintaining a shared vision and focus on continuous improvement of the products and processes to achieve the set quality objectives

Meeting all current requirements of National and International regulations.

NATEC Medical Limited Quality Management System complies with:

21 CFR part820 and FDA requirements

Latest versions of ISO13485 standards

ISO14971 for our risk management system, European Directive for Medical Devices 93/42/CEE

NATEC Medical Limited is registered with the FDA (#3004415014).

Our Medical Devices are either CE marked and/or 510(k) registered by our experienced regulatory team.

The human factor is a key critical factor in any production process, NATEC Medical considers employee training key to NATEC success.

Wherever possible Natec strive to build in Quality in each of its process to meet customer requirements rather than just qualifying the process.

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