Service and Support
Like all reusable medical devices, the SterilContainer System requires inspection prior to use, and proper care and handling.
The Aesculap SterilContainer System is a FDA Class II device that requires extensive testing and FDA 510(k) clearance. An Aesculap trained technician can repair containers to the original equipment manufacturer dimensions and specifications of the original containers used in the validation and replace parts such as gaskets, filter systems and handles with the same Aesculap components.
ONLY Aesculap trained technicians are authorized to repair the Aesculap SterilContainer System. Using a non-Aesculap repair technician to repair containers will void the Aesculap Warranty on the container and may void any of the validation testing associated with Aesculap containers.
