I agree. The term “reprocessed single-use device” actually doesn't often make sense. The reality is that an original equipment manufacturer, at the point where they are starting to think about a new device, goes through a rigorous exercise of how to design it, how to develop it, and how to validate it. That leads to licensing. As for the point at which they are looking at what materials, how the device is going to be used, and what sort of durability there is, that whole exercise is a pretty rigorous one.
The fact is that we now have reprocessing companies that are regulated in the United States and think they can now, through their proprietary technology and expertise, take a single-use device and reprocess it. Our view is that we should be asking them to prove it. Right now, Health Canada—