Guarda Medical's continuous commitment to patient safety and the quality of medical services aims to offer a wide range of tests and verification procedures. This is to ensure that the sterilization process is highly effective and medical devices are completely safe for use in any clinical context. Thanks to our dedication to technology, we tirelessly work to provide reliable and innovative solutions that meet the most demanding requirements in healthcare.

The validation of the sterilization process of medical devices (sterilizers, thermal disinfectors, heat sealers, and sterile barrier systems) is an annual or semi-annual activity to ensure that the devices used for sterilization are capable of delivering reliable and repeatable results over time. They must comply with the standards for cleaning and sterilization prescribed by applicable regulations.

This process includes a series of tests and controls, including the physical and microbiological qualification of the equipment in the sterilization center, analysis of steam and water quality, functionality verification and calibration of control instruments, analysis of chemical and protein residues, and verification of the sterility of medical devices.

The SERVICE OFFERED FOR THE VALIDATION OF STERILIZATION EQUIPMENT by us includes the following:

  • Sink washers: UNI EN 15883-3
  • Endoscope cleaning devices: UNI EN 15883-4
  • Instrument cleaning devices: UNI EN 15883-1-2-5
  • Packaging: UNI EN 11607-1-2 and 868
  • Steam sterilizers: UNI EN 285 and UNI EN 17665