Description
The Interim Order (IO) expedites the authorization of Class I to IV medical devices used for COVID-19: sets out the safety, effectiveness and quality requirements for filtering facepiece respirators (FFRs), and provides criteria for Canadian manufacturers developing respirators in Canada.
Resources
| Name | Format | Description | Link |
|---|---|---|---|
| Guidance on safety and performance specifications for filtering facepiece respirators (FFRs) during COVID-19: Background | HTML | Open resource | |
| Guidance on safety and performance specifications for filtering facepiece respirators (FFRs) during COVID-19: Background | HTML | Open resource |