Anonymous
Guest
Anonymous
Guest
Does Ascent open the device up and disassemble the product down to it's original components each time it cleans it? No. Then how can you claim these devices are clean?
With all the differences between similar devices, I'd like to see how this fly by night company validated the cleaning and sterility of each product. I would bet big money they didn't test each companies product they claim they can clean.
Fly by night??? Hilarious! That's what you are telling the docs at your sponsored dinners. Which is fine, we may lose a little business now with your stupidity. But, they will come back once they see the facts. Nice ad by the way: "Take a closer look." I lost business for two weeks on the scalpal, until I showed them the studies were done in an Oklahoma facility (partially owned by J&J) and a facility in Canada (outside FDA jurisdiction). The doc scoffed and shook his head. He also asked me about the FDA website his Ethicon rep pointed him to that said reprocessing of class 3 devices is not recommended. My response: "And yes sir, I agree with you. We shouldn't reprocess class 3 devices. That is why we only stick to class 1 and 2. Dr, the rep who pointed you to this loves giving you partial info and letting get upset that your hospital allows these devices back in your cases. But, keep in mind, they don't have the balls to take anything to the FDA."
Because then Ascent would get a clearence letter from the FDA and all this brew haha would be over.