Foreign risk notification for medical devices guidance document: Responsibilities and notifiable actions (French, HTML)

View metadata and access the original French HTML file: Foreign risk notification for medical devices guidance document: Responsibilities and notifiable actions.

Format

HTML

Access

file-only

Publisher-reported update

2024-03-30

Medical device licence holders and importers of Class II to IV devices must notify Health Canada when there’s a serious risk of injury to human health concerning a device authorized for sale in Canada

Access original file