{"id":447514,"title":"Mandatory Medical Device Problem Reporting Form for Industry - Canada.ca","sourceCode":"hc","sourceName":"Health Canada","language":"en","captureDate":"2026-01-03","captureTimestamp":"2026-01-03T14:38:57.470000+00:00","jobId":6,"originalUrl":"https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting/mandatory-medical-device-problem-reporting-form-industry-adverse-reaction-reporting.html?wbdisable=false","snippet":"Mandatory Medical Device Problem Reporting Form for Industry HC Pub.: 110180 (April 2018) This HTML document is not a form. Its purpose is to display the information as found on the form for viewing purposes only. If you wish to use the form, you must use the alternate format…","rawSnapshotUrl":"/api/snapshots/raw/447514","browseUrl":"https://replay.healtharchive.ca/job-6/20260103143857/https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting/mandatory-medical-device-problem-reporting-form-industry-adverse-reaction-reporting.html?wbdisable=false#ha_snapshot=447514","mimeType":"text/html","statusCode":200,"captureBackend":"browsertrix","captureFidelity":"high"}