The requirements of cleaning, reprocessing and sterilization procedures of medical devices can be divided into two product categories:

  1. Cleaning and sterilization of medical devices delivered in a sterile state
  2. Cleaning, reprocessing and sterilization of reusable medical devices (ISO 17664)

Both product categories have in common that validated sterilization processes can only be applied to devices which are clean and disinfected. Cleaning and disinfection are therefore prerequisites for any effective sterilization process. All processes need to be subjected to validation studies.

What we offer:

  • Cleaning and sterilization of medical devices delivered in a sterile state
  • Cleaning, reprocessing and sterilization of reusable medical devices
  • Validation of sterilization processes

Contact us for a free proposal on testing related to ISO 17664.