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


CKAN dataset id 30d35e79-ad1e-403d-bbc7-3da378a3f6e4
상태 active
버전 2024-03-30
라이선스 ca-ogl-lgo
담당자 연락처
제공 기관 Health Canada
최초 수집 일시 2024-06-12T12:29:46…
최근 수집 일시 2024-06-12T12:29:46…

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