If we have different approvals (different intended use, indications for use) on different markets, should we have different websites for each specific market (which is different than "international") or the disclaimer/footnote on the webside (draft example: "...this website is for EU... for countries where specific national approvals or clereances are required some applications may not have been cleared yet...please check by the manufacturer or your national regulatory body to find the applications that are available for sale and use...") should be sufficient?
Does anyone know any requirement (FDA, Health Canada or others) related to this?
Does anyone know any requirement (FDA, Health Canada or others) related to this?