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Medical Devices Regulations (SOR/98-282)

Regulations are current to 2024-06-11 and last amended on 2024-01-03. Previous Versions

 No person shall advertise for the purpose of sale a Class I medical device for which the manufacturer holds an authorization if the device has been subjected to a change described in section 68.13 unless

  • (a) the manufacturer holds an amended authorization; or

  • (b) the advertisement is placed only in a catalogue that includes a clear and visible warning that the devices advertised in the catalogue may not have been authorized in accordance with Canadian law.


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