Bringing medical innovations to life

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Why work with Mi3?

Our people are our proof. Our experts have joined us from various disciplines, including medical, pharma and regulatory backgrounds – we are uniquely positioned to provide professional advice on all elements of your product creation.
From your initial consultation, right through to the manufacturing and distribution of your product, our experts are with you every step of the way. Advising, designing and collaborating. We are your partner in complex plastics.
We take your bright idea from consultation to concept to production, through established medical device development processes. Together, we bring medical innovations to life.  
“Mi3 has a customer focus culture and it is dedicated to helping solve issues and improve output quality. Medela AG has seen how Mi3 is passionate about assisting us to scale up the business”. 
Daniele Samuel Pascovici, Project Sourcing Healthcare, Medela AG

Design & New Product Development

Whether looking for concept and design, tool design or tool making, our experts work closely with you to ensure that your medical device is designed and developed exactly as you intended. We follow 7 key phases, from concept to design transfer to manufacturing, with each stage followed by a gated review to ensure a seamless collaboration between us and you.


Our purpose-built ISO 14644 compliant Class 7 clean-room facility has been designed for precise manual and automated assembly of medical devices, including IVDs. High tolerance injection moulding and ultrasonic welding is also available in our secondary Class 8 clean room. Through validated processes and regular training programmes, we ensure the manufacture of your medical device is in the safest of hands.


Our experts help identify the ideal medical sterilisation method for your product, and can offer customised solutions, created using data from live validations. Our sterilisation processes include Gamma Irradiation and Ethylene Oxide, and all sterility is performed in accordance with ISO guidelines.