Foreign risk notification for medical devices guidance document: Responsibilities and notifiable actions

Medical device licence holders and importers of Class II to IV devices must notify Health Canada when there’s a serious risk of injury to human health concerning a device authorized for sale in Canada

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Title (French) Lignes directrices sur la notification des risques survenus à l’étranger liés aux instruments médicaux : Responsabilités et mesures à déclaration obligatoire
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Open Canada Date Published 2022-03-09 00:00:00
Open Canada Date Modified
Open Canada Subject ["health_and_safety"]
Open Canada Keywords {"fr": ["Notification des risques étrangers", "dispositifs médicaux", "document d'orientation", "responsabilités", "actions à notifier"], "en": ["Foreign risk notification", "medical devices", "guidance document", "responsibilities", "notifiable actions"]}
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