Medical Devices Regulations

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.