Medical Devices Regulations
Version of section 88 from 2006-03-22 to 2021-06-22:
88 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 mandatory problem reporting;
(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
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