I agree Geoff but once it's within the framework of CE and classified as a medical device it's up to good people like ourselves to report "issues" to the competent authority, i.e. MHRA, so they they or the manufacturer can take appropriate action, if necessary, to sort it out. It's better than the "bad old days" when, for example, equipment with American colour-coded mains parts was supplied in this country and other devices that I would classify as unsafe under any circumstances was being manufactured and sold by every TDH company out to make a few bob. What more acceptable alternative would you suggest Geoff?
