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Medical Devices Regulations

Version of section 39 from 2016-07-17 to 2020-09-09:


 If the Minister believes on reasonable grounds, after reviewing a report or information brought to the Minister’s attention, that a licensed medical device may not meet the applicable requirements of sections 10 to 20, the Minister may request the manufacturer to submit, on or before a specified day, information or samples to enable the Minister to determine whether the device meets those requirements.

  • SOR/2015-193, s. 7
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