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Medical Devices Regulations

Version of section 68.22 from 2023-02-22 to 2024-01-02:


 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

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