{"id":432546,"title":"Mandatory Medical Device Problem Reporting Form for Industry - Canada.ca","sourceCode":"hc","sourceName":"Health Canada","language":"en","captureDate":"2026-01-02","captureTimestamp":"2026-01-02T08:18:27.983000+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","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/432546","browseUrl":"https://replay.healtharchive.ca/job-6/20260102081827/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#ha_snapshot=432546","mimeType":"text/html","statusCode":200,"captureBackend":"browsertrix","captureFidelity":"high"}