Consultation on Medical Devices Product Classification Guide

The Medical Devices Branch (MDB) has published a draft document “Medical Devices Product Classification Guide” for comments. This document is intended to assist our stakeholders in determining whether a product is classified as a medical device. We would like to invite our stakeholders to provide feedback on this document:

Medical Devices Product Classification Guide1857 KB

The Consultation period for this document is from 15 March 2021 to 15 April 2021. Please email your feedback using the prescribed feedback form to by 15 April 2021. Please indicate " Medical Devices Product Classification Guide" in the email subject header.

guidance-feedback-form14 KB

Healthcare professional, Industry member, Medical devices

Regulatory Updates