{"id":625830,"title":"Guidance Document - Guidance on the Risk-based Classification System for Non-In Vitro Diagnostic Devices (non-IVDDs) - Canada.ca","sourceCode":"hc","sourceName":"Health Canada","language":"en","captureDate":"2026-02-27","captureTimestamp":"2026-02-27T15:58:13.604000+00:00","jobId":6,"originalUrl":"https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/guidance-document-guidance-risk-based-classification-system-non-vitro-diagnostic.html","snippet":"Guidance Document - Guidance on the Risk-based Classification System for Non-In Vitro Diagnostic Devices (non-IVDDs) Publish by authority of the Minister of Health (PDF Version - 172 K) Date Adopted: 2015/04/23 Effective Date: 2015/06/12 Health Products and Food Branch Our…","rawSnapshotUrl":"/api/snapshots/raw/625830","browseUrl":"https://replay.healtharchive.ca/job-6/20260227155813/https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/guidance-document-guidance-risk-based-classification-system-non-vitro-diagnostic.html#ha_snapshot=625830","mimeType":"text/html","statusCode":200,"captureBackend":"browsertrix","captureFidelity":"high"}