Learn more about definition, procedures and tests according to DIN EN ISO 17664-1/-2 and DIN EN ISO 17665
The safe reuse of medical devices is a key component of patient safety. Validating reprocessing procedures in accordance with DIN EN ISO 17664-1/-2 and DIN EN ISO 17665 ensures that the cleaning, disinfection, and sterilization processes specified by the manufacturer are effective and reproducible. The accredited testing laboratory plays a crucial role in testing the described procedures under accredited and monitored laboratory conditions.
In this article, you will learn more about the validation of the preparation instructions.
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