{"id":392136,"title":"Designated Devices Registry Guidance Document - Canada.ca","sourceCode":"hc","sourceName":"Health Canada","language":"en","captureDate":"2026-04-14","captureTimestamp":"2026-04-14T08:02:06.590000+00:00","jobId":6,"originalUrl":"https://www.canada.ca/en/health-canada/services/meeting-legal-requirements-manufacturing-drug-health-products/guidance-document.html","snippet":"Designated device registration guidance document for new and existing registrants Definition of designated device Designated device means a device included in Schedule IX of the Controlled Drugs and Substances Act . Pill press: Manual, semi-automatic or fully automatic device —…","rawSnapshotUrl":"/api/snapshots/raw/392136","browseUrl":"https://replay.healtharchive.ca/job-6/20260414080206/https://www.canada.ca/en/health-canada/services/meeting-legal-requirements-manufacturing-drug-health-products/guidance-document.html#ha_snapshot=392136","mimeType":"text/html","statusCode":200,"captureBackend":"browsertrix","captureFidelity":"high"}