Medical Devices Regulations
Version of section 39 from 2016-07-17 to 2021-06-22:
39 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
- Date modified: