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Eyetec is inserted in a productive sector that is highly regulated, that is, it serves the manufacture of medical and electromedical products and equipment. For this, we have mastered the technical and scientific knowledge to develop and launch new products. Eyetec controls the entire production process to meet the numerous norms and legal requirements required for this segment. Quality is our strategic issue. In conclusion, we maintain a prominent position in this segment. With this vision in mind, we inaugurated in 2009 a new plant with 3,000 m2, fully adapted to international standards for the manufacture of medical equipment and obtaining ISO 9001, ISO 14000, ISO 13485, FDA, CE certifications and INMETRO, necessary for the manufacture of electromedical equipment, in addition to the requirements of the ANVISA such as Good Manufacturing Practices.


Eyetec is a company certified by ANVISA in the Good Manufacturing Practices RDC 16 of 2013. This certificate guarantees that the company has a quality management system in compliance with the legal requirements of production, distribution, transportation and Technical Assistance for Medical Equipment and related. In conclusion, it guarantees customers a fully controlled, tracked process that meets international requirements for the manufacture of medical equipment.


The quality policy must be known to all employees of the company, as it is what dictates the guidelines for the entire Quality Management system of the company: “Establishing goals within a Quality Standard, aiming at the continuous improvement of our processes , raise awareness and commit our employees to the importance of quality applied to our products and services ”. That is why, when purchasing an Eyetec product, you will have the peace of mind of meeting the legal requirements for the operation of clinics and hospitals with regard to the control, acquisition and maintenance of medical equipment.

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