New labelling and MDEL requirements for medical devices authorized under interim orders on September 1, 2021

Name: New labelling and MDEL requirements for medical devices authorized under interim orders on September 1, 2021
Creator: Health Canada
License: https://open.canada.ca/en/open-government-licence-canada

Labels of IO-authorized devices must be, at a minimum, in either English or French. There are also several additional requirements (for example, bilingual labelling) depending on whether the device is to be sold to the general public.

Publisher: Health Canada
Resources: 2
Catalogue metadata updated: 2023-02-27

Data overview

Formats: HTML
File languages: English, French

Official sources and licences

Government of Canada Open Data
Open Government Licence – Canada

Resources

New labelling and MDEL requirements for medical devices authorized under interim orders on September 1, 2021 (French, HTML) HTML
New labelling and MDEL requirements for medical devices authorized under interim orders on September 1, 2021 (English, HTML) HTML

Related open data

Health Canada