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Browse and search historical snapshots. This is an archive — not current guidance or medical advice. Archived content may be incomplete, outdated, or superseded. For up-to-date recommendations, always consult the official source website.

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Medical device meetings draft guidance document: Appendices Overview Guidance for implementation Appendices On this page Device Advice: Meeting process map Innovation information meeting record of decision template Pre-clinical meeting record of decision template Pre-submission…

Medical device meetings draft guidance document: Guidance for implementation Overview Guidance for implementation Appendices On this page Operating principles Meeting types and their eligibility criteria Combination products How to request a meeting Meeting package Where to file…

Draft guidance for reporting medical device shortages: Definitions and instructions Background Who must report What must be reported When and how to report What happens to your report Definitions and instructions Health Canada has made the medical device shortage reporting…

Draft guidance for reporting medical device shortages: What happens to your report Background Who must report What must be reported When and how to report What happens to your report Definitions and instructions Health Canada has made the medical device shortage reporting…

Draft guidance for reporting medical device shortages: When and how to report Background Who must report What must be reported When and how to report What happens to your report Definitions and instructions Health Canada has made the medical device shortage reporting framework…

Draft guidance for reporting medical device shortages: What must be reported Background Who must report What must be reported When and how to report What happens to your report Definitions and instructions Health Canada has made the medical device shortage reporting framework…

Draft guidance for reporting medical device shortages: Who must report Background Who must report What must be reported When and how to report What happens to your report Definitions and instructions Health Canada has made the medical device shortage reporting framework permanent…

ARCHIVED List of Regulatory Agencies for the Purposes of Subsection 68.11(4) of the Medical Devices Regulations (2023-02-23 to 2024-01-02) Notice to Reader This is an archived list. Please refer to the most current version of this list. Date issued: 2023-02-22 This list is…

ARCHIVED Authorization of medical devices for an urgent public health need: List of medical devices for expanded use (2024-01-03 – 2024-03-18) Notice to Reader This is an archived list. Please refer to the most current version of this list. The List of Medical Devices for…

Regulating certain ultraviolet radiation-emitting and ozone-generating devices under the Pest Control Products Act: Compliance and enforcement of the Act Overview Devices subject to the Act Devices not subject to the Act List of registered devices Compliance and enforcement of…

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