QUALITY CERTIFICATIONS

CID is committed to design, develop, manufacture, distribute and market its devices with the intent to:

Provide advanced Medical Devices of absolute quality, safety, efficacy and reliability,in order to restore patient health and well-being.

Quality Policy Declaration

QUALITY POLICY DECLARATION

  • Maintaining an efficacy quality system with the appropriate resources and monitoring the correct implementation in all the company departments;
  • Empowering and enhancing company resources through appropriate trainings and a continuous updating;
  • Implementing reliable partnerships with our Suppliers;
  • Collaborating with the national and international medical community and competent authorities in order to strengthen a reliable and ethic partnership;
  • Focusing on Patient safety and well-being by offering Physicians devices to reduce risks, trauma, procedure times and recovery.
Quality Management System

Quality Management System of CID is certified ISO 9001 and ISO 13485 by TUV SUD Group, including conformity to Canadian Medical Device Regulation.

Medical Devices manufactured by CID are placed at the highest classes of their category. They are marked CE by the Istituto Superiore di Sanità
(NB 0373) according to the EU Medical Device Directive (MDD).

These certifications allow CID to market its devices in over 80 countries around the world, excluding USA and Japan.

EN ISO13485-2003 ISO9001:2008 ISO13485-CMDR

EN ISO13485-2003

ISO9001:2008

ISO13485-CMDR