Foreign risk notification for medical devices guidance document: Responsibilities and notifiable actions
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
- Publisher
- Health Canada
- Resources
- 2
- Catalogue metadata updated
- 2024-03-30
Data overview
- Formats
- HTML
- File languages
- English, French