Cleaning Validation
Cleaning validation is performed for reusable medical devices to ensure that an appropriate amount of the contaminants (such as oils, tissues, soil, microorganisms, etc.) a medical device has been exposed to during intended use have been removed from the device during the cleaning process. Quantification of contaminant volume on reusable devices following proscribed cleaning processes ensures that the microbial and soil load of the device is low enough that successful re-sterilization of the device can occur between procedures consistently.
Our Tests
M415P
Pre-Vacuum Steam Sterilization Validation
M416
Manual Cleaning Validation Study
M418P
Pre-Vacuum Dry Time Validation
Sample Submission
Purchase Order
In line with current ISO/QSR purchasing requirements, all orders should be sent with a signed completed Purchase Order. This will help expedite the processing or your order. Standing Purchase Orders will be gladly accepted for routine continuing orders.
Sample Submission Form
Final Reports
Upon completion of test, a final report will be issued and all records and raw data will be held for five years.
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