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Medical Devices Regulations

Version of section 88 from 2021-06-23 to 2022-09-11:


 The requirements set out in the following provisions apply to medical devices to which this Part applies:

  • (a) sections 52 to 56 with respect to distribution records;

  • (b) sections 57 and 58 with respect to complaint handling;

  • (c) sections 59 to 61.1 with respect to reports on incidents;

  • (d) sections 63 to 65.1 with respect to recalls; and

  • (e) sections 66 to 68 with respect to implant registration.

  • SOR/2002-190, s. 9
  • SOR/2020-262, s. 21
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