Health Canada Medical Device Reporting Database

Incident reporting for medical devices: Guidance document

https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/incident-reporting-medical-devices-guidance-2021.html

Canada Vigilance - Medical Device Problem Reporting Program Marketed Health Products Directorate Health Canada Address Locator 0701E 200 Tunney's Pasture Driveway Ottawa, Ontario K1A …

Drug and Medical Device Databases - Canada.ca

https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/applications-submissions/guidance-documents/drug-and-medical-device-databases.html

Medical Devices Active Licence Listing (MDALL)

https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/licences/medical-devices-active-licence-listing.html

The Bureau maintains a database of all licensed Class II, III, and IV medical devices offered for sale in Canada. Class I medical devices do not require a medical device …

Adverse Reaction Database - Canada.ca

https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-database.html

Guidance on summary reports and issue-related analyses for medical devices: Overview [2021-01-14] Notice: New regulations strengthening the post-market surveillance and risk …

Medical devices - Canada.ca

https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices.html

The term Medical Devices, as defined in the Food and Drugs Act, covers a wide range of health or medical instruments used in the treatment, mitigation, diagnosis …

Adverse reactions, medical device incidents and health …

https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/adverse-reactions-incidents-recalls-2019-summary.html

each year, more suspected products are being reported in the medical device incidents sent to Health Canada from 6,544 devices in 2010 to 25,519 devices in 2019, a 4-fold …

Mandatory Medical Device Problem Reporting Form for …

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

How to Submit the Report. Completed forms should be emailed to: [email protected] or faxed to: 1-866-678-6789 or mailed to: Canada Vigilance - Medical Device …

Medical Device Incidents - Drug and Health Product Register

https://hpr-rps.hres.ca/mdi_landing.php

Search Medical Device Incidents. Search for term (s) Download Full Extract. Disclaimer. Date modified: 2021-07-14.

The drug and health products inspections database …

https://www.canada.ca/en/health-canada/services/inspecting-monitoring-drug-health-products/drug-health-product-inspections.html

The Drug and Health Products Inspections Database (DHPID) supports open government and regulatory transparency. It: gives you access to information about each type of drug …

Health Canada Medical Device Adverse Event Reporting - Emergo

https://www.emergobyul.com/services/health-canada-adverse-event-reporting-medical-devices

Canada Medical Device Reporting Process. Here are the basic steps you should follow in reporting an adverse event in Canada: Refer to your written Standard Operating …