Guidance Document – Supporting Evidence for Implantable Medical Devices Manufactured by 3D Printing - Summary

From: Health Canada

Overview

This guidance document is intended to aid manufacturers and regulatory representatives in preparing medical device licence applications for 3D-printed medical devices.

Who this guide is for

Medical Device manufacturers

In this guide

View complete guide

Download PDF (271 KB, 18 pages)

Details and history

Published: April 30, 2019

Consulted: November 8, 2018 - January 8, 2019

Part of topic(s): Guidance on legislation, medical devices and 3D printing

For assistance

Our service hours are Monday to Friday from 8 a.m. to 6 p.m. (local time).  Closed on statuary holidays.

By email: devicelicensing-homologationinstruments@hc-sc.gc.ca

Page details

Date modified: