Sterilization and Processing
Manufacturers of medical devices are required by EN ISO 17664:2004 to provide information about the sterilization process requirements of their medical products.
ulrich medical® has fulfilled this obligation and categorizes our medical devices in product groups.
The groups were then validated as required in paragraph 5 of EN ISO 17664:2004. The validation tests were based on the product with the most critical design or material of each group.
These tests were completed by the Laboratories Qualis in Konstanz and MTD in Ochsenhausen, Germany. ulrich medical® classifies its medical devices based on the most distinctive and self explanatory characteristic of each product.