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  1. Medical Devices Regulations - SOR/98-282 (Section 87)

     No person shall advertise a medical device that is the subject of investigational testing unless

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    • (b) the advertisement clearly indicates that the device is the subject of investigational testing, and the purpose of the investigational testing.


  2. Medical Devices Regulations - SOR/98-282 (Section 31)
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    • (2) If a medical device group is licensed, all the medical devices that form part of the medical device group are deemed, for the purposes of its importation, sale or advertisement, to have been licensed.


  3. Medical Devices Regulations - SOR/98-282 (Section 29)

     If a test kit is licensed, all of its reagents or articles that are manufactured by the manufacturer of the test kit are deemed, for the purposes of its importation, sale or advertisement, to have been licensed.


  4. Medical Devices Regulations - SOR/98-282 (Section 28)

     If a system is licensed, all of its components or parts that are manufactured by the manufacturer of the system are deemed, for the purposes of its importation, sale or advertisement, to have been licensed.


  5. Medical Devices Regulations - SOR/98-282 (Section 27)

     No person shall advertise a Class II, III or IV medical device for the purpose of sale unless

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    • (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 licensed in accordance with Canadian law.

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