Changes

'''This tool is intended to assist you with the classification of your medical device by walking through the classification rules found in Schedule 1 of the ''[https://laws-lois.justice.gc.ca/eng/regulations/SOR-98-282/FullText.html Medical Devices Regulations]'' (the Regulations).  It is only intended to classify medical devices that fit the definition of a “device” in the ''[https://laws-lois.justice.gc.ca/eng/acts/f-27/FullText.html Food and Drugs Act]'' and a “medical device” into Class I, II, III or IV. It will not indicate that your product is not a medical device, nor that it fits under another category (e.g. drug, consumer product).  You will need to determine that your product fits the definition of a “medical device” prior to using this tool.'''

'''This tool is intended to assist you with the classification of your medical device by walking through the classification rules found in Schedule 1 of the ''[https://laws-lois.justice.gc.ca/eng/regulations/SOR-98-282/FullText.html Medical Devices Regulations]'' (the Regulations).  It is only intended to classify medical devices that fit the definition of a “device” in the ''[https://laws-lois.justice.gc.ca/eng/acts/f-27/FullText.html Food and Drugs Act]'' and a “medical device” into Class I, II, III or IV. It will not indicate that your product is not a medical device, nor that it fits under another category (e.g. drug, consumer product).  You will need to determine that your product fits the definition of a “medical device” prior to using this tool.'''