Medical Devices Regulations
Version of section 68.22 from 2023-02-22 to 2024-01-02:
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.
- SOR/2023-19, s. 7
- Date modified: