Certification ISO 13485 : 2016

Our company is pleased to announce that we will be achieving ISO 13485 in 2020.
ISO 13485: 2016 sets out requirements for a quality management system where an organization must demonstrate its ability to regularly provide medical devices and related services in accordance with client requirements and applicable regulatory requirements. This allows us to manufacture, sell and export our cannulas (non-invasive and non-implanted medical components.
ISO 13485

Our expertise

A long tradition of research, innovation and quality allows us to guarantee the manufacture of your products in total agreement with your requirements.