Tequir, Innovation
Services

Medical Devices
consultancy

Preparation of CE
marking technical files

Implementation of Quality Management System based on ISO 13485
Projects

KEEP WALKING. Femoral Implant.
The distal loading implant for transfemoral amputees is one of our main development projects.
In 2014 we obtained CE marking and currently have the product registered with various European and international health agencies. The device was registered with the TGA and has recently been included in the Australian Prostheses List.
SINCE 1998
Tequir Certifications

EN ISO 13485
ISO 13485 is an internationally recognised standard for quality management systems in the medical device industry. It is intended and conceived for use in organisations for the design and development, production, installation, services, and sales of medical devices. At Tequir we have had this standard since 2003.