Health Canada HCHC Guidance — Devices
HC Guidance — Devices is the official HC identifier for “Guidance for the Labelling of Medical Devices, not including in vitro diagnostic devices”. HC Guidance — Devices is the official identifier HC uses for this instrument.
- Instrument
- HC
- Full name
- HC Guidance — Devices
- Category
- Labeling
- Authority source
- English
- Readable HTML
- 5 articles · 1 language version
- Published
- June 12, 2004
- Effective
- —
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Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Guidance for the Labelling of Medical Devices, not including in vitro diagnostic devices
Complete Health Canada labelling guidance for medical devices other than IVDs, walked regulation-by-regulation through Medical Devices Regulations sections 21-24 (label contents, outer package, bilingual s. 23 requirements, and electronic labelling conditions) plus the two appendices for soft/decorative contact lenses and menstrual tampons published on the same page. Foreword document control: adopted 12 June 2004, version date 15 June 2015 (replaces the 2014-06-12 version). The URL slug ("including-vitro-diagnostic-devices-appendices") is stale; the current page title governs. Ingested from the exact official HTML with a foreword preamble (document control block incl. change log) and sec-1..sec-5 section anchors.
HC Guidance — Devices is the official identifier HC uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.