FREE Consultation with Mi3’s COVID Experts
At Mi3, we are the experts in end-to-end manufacturing of your COVID diagnostic devices. We take your bright idea from consultation to concept to production, and work alongside you to bring your diagnostic and antibody testing solution to life.
Mi3 adheres to the highest international industry standards compliant to ISO 14644 which governs the operation of cleanrooms with respect to the assembly of medical devices. Our experts will advise you on the best solution for your product at any stage of your product development which covers:
- Product concept development
- 3D prototype printing
- Designing the COVID diagnostic device
- Manufacturing in high-end Class 7 & 8 cleanroom facilities
- Antibody testing
- Distribution of the COVID diagnostic device
Book your free consultation today to discuss how Mi3 can bring your medical product to life!
Why work with Mi3?
COVID Diagnostic Devices
From concept to creation, Mi3 are on hand to bring your COVID diagnostic device to life. From our sterile, ISO 14644 compliant Class 7 and class 8 clean room facilities, our experts can produce and distribute your diagnostic and antibody testing solutions. We’ll work closely with you to ensure that your COVID diagnostic device is designed and developed exactly as you intended – ensuring sterility and regulatory compliance every step of the way.
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.