Medical technology according to MDR and ISO 13485 – your partner for safe innovations
Since 1982, MIPM has stood for quality and precision in the development of MRI-compatible medical technology. As a certified company, we develop according to DIN EN ISO 13485 and meet the requirements of the Medical Device Regulation (MDR) – for maximum safety and reliable performance.
Our processes are based on state-of-the-art technology and follow a clear step-by-step model that makes the path from idea to CE-compliant market launch transparent.
And more: We are happy to support you with global approvals, for example in the USA with FDA 510(k), to position your products successfully internationally.
Your advantage: You receive products that meet the highest regulatory standards – developed with experience, innovation, and uncompromising quality.
