Changes

It is only intended to classify products that meet 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 is only intended to classify products that meet 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** determine whether your product is *not* a medical device or if it falls under another category (e.g., drug, consumer product).   

It will not determine whether your product is not a medical device or if it falls 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.

You will need to determine that your product fits the definition of a “medical device” prior to using this tool.