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