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		https://www.canada.ca/en/health-canada/services/drugs-health-products/covid19-industry/medical-devices/personal-protective-equipment/medical-masks-respirators/safety-performance-specifications.html
Guidance on safety and performance specifications for filtering facepiece respirators (FFRs) during COVID-19: Background	HTML		https://www.canada.ca/fr/sante-canada/services/medicaments-produits-sante/covid19-industrie/instruments-medicaux/equipement-protection-individuelle/masques-medicaux-respirateurs/criteres-securite-rendement.html

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