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 Medical Devices Regulations.  Please note that the tool will provide classification guidance based strictly on how you answer the questions herein.  This classification guidance should not be taken as a final decision by Health Canada'''

'''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 Medical Devices Regulations.  Please note that the tool will provide classification guidance based strictly on how you answer the questions herein.  This classification guidance should not be taken as a final decision by Health Canada'''

= '''[https://forms.office.com/Pages/ResponsePage.aspx?id=FZD9Qk3eI0KjaLrqyrSJJyG_2PeVuVlHvSZss2grfWZUNTNISU9QT1YyOUNWRDhNN1g5Wk9RWVVXUi4u Classification Tool]''' =

= '''[https://forms.office.com/r/uuGZEqtiBi Classification Tool]''' =

'''''*When using this tool to classify Software as a Medical Device (SaMD), please refer to the SaMD guidance documents below to understand Health Canada's interpretation of terms such as "immediate danger" in this context.'''''

'''''*When using this tool to classify Software as a Medical Device (SaMD), please refer to the SaMD guidance documents below to understand Health Canada's interpretation of terms such as "immediate danger" in this context.'''''