Our challenge

Ensuring that complex medical devices meet the highest safety standards to protect patients and clinicians remains a significant challenge. Regulatory requirements for remanufacturing continuously evolve alongside advances in state-of-the-art practices. The new EU regulations mandate identical quality standards for medical remanufacturers as for original equipment manufacturers. Procurement organizations face the challenge of acquiring high-quality medical devices within limited budgets, especially during global pandemics.

Our mission

With certified, state-of-the-art processes, we have set global standards in medical remanufacturing for the past 25 years. Our innovative remanufacturing processes, rooted in the circular economy concept, involve disassembling used products, rigorous cleaning, testing, and multiple quality and safety controls. Unlike relying on batch testing, we ensure that 100% of our products undergo individual checks for safety and performance. This guarantees that remanufactured medical devices are restored to “as new” functional and safety standards, fully complying with all EU regulatory requirements.

Our solution

Our remanufactured devices are restored to meet “as new” functional and safety standards. All our cleaning machines, workplaces, and test stations have been developed by our Research and Development team in collaboration with scientific institutions. They are specifically tailored to the remanufacturing of complex medical devices. Our Research and Development team works continuously on innovating new products and processes.

We operate independently of the original equipment manufacturers, empowering our customers to reuse a wide variety of complex single-use medical devices.