Do you manufacture reusable medical devices?
If so, your products are likely used in medical facilities around the world.
In the EU, manufacturers wanting to sell reusable medical devices must ensure that their cleaning, disinfection, and sterilisation procedures are validated.
SAXOCON has the expertise to help you get your procedures into compliance with all relevant guidelines, such as AAMI TIR12 and ISO 17665, and keep your products on the market or get your new products approved quickly.