Medical Devices Regulations
Version of section 68.22 from 2024-01-03 to 2024-10-30:
68.22 An authorization for a 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 holder has discontinued the sale of the device in Canada.
- SOR/2023-19, s. 7
- SOR/2023-277, s. 14(E)
- SOR/2023-277, s. 25
- Date modified: