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Medical Devices Regulations

Version of section 68.2 from 2023-02-22 to 2024-01-02:


 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

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