Medical Devices Regulations

68.22 An authorization for a COVID-19 medical device is cancelled if

• (a) in the case of a Class I device, the holder of the authorization is issued an establishment licence under section 46 that authorizes the holder to sell or import the device;

• (b) in the case of a Class II, III or IV device, the holder of the authorization is issued a licence for the device under section 36; or

• (c) the holder of the authorization informs the Minister under section 68.25 that the sale of the device has been discontinued in Canada.