Medical Devices Regulations
Version of section 68.2 from 2023-02-22 to 2024-01-02:
68.2 Despite section 68.03, the holder of an authorization for a COVID-19 medical device may submit
(a) in the case of a Class I device, an application under section 45 for an establishment licence that would authorize the holder to sell or import the device; or
(b) in the case of a Class II, III or IV device, an application under section 32 for a licence for the device.
- SOR/2023-19, s. 7
- Date modified: