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Medical Devices Regulations

Version of section 68.13 from 2024-01-03 to 2024-11-11:


 No person shall import or sell a medical device for which the manufacturer holds an authorization if the device has been the subject of any of the following changes unless the manufacturer holds an amended authorization:

  • (a) in the case of a Class III or IV device, a significant change;

  • (b) a change that would result in a change of the class of the device;

  • (c) a change in the name of the manufacturer;

  • (d) a change in the name of the device;

  • (e) a change in the identifier of the device, including the identifier of any medical device that is part of a system, test kit, medical device group, medical device family or medical device group family;

  • (f) in the case of a Class I or II device, a change in the medical conditions, purposes or uses for which the device is manufactured, sold or represented.

  • SOR/2023-19, s. 7
  • SOR/2023-277, s. 11
  • SOR/2023-277, s. 25

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