Safety and quality are non-negotiable in the medical devices industry. As a commitment, our Quality Management System was first certified to ISO 13485:2016 in 2018. Since then we have maintained our certification, assured by annual QMS audits.
ISO 13485 ensures the consistent design, development, production, installation and delivery through to disposal of our medical devices that are safe for their intended purpose.
Certificate copy can be provided upon request. Consult our support documentation section for more details.
