Canada
Medical device market intelligence for Canada. Regulatory changes, competitor moves, and procurement trends.
Last 7 days
Bolle (Canada) Inc has registered with the FDA under product code HQY.
The Micra MC1VR01 device has been recalled due to safety concerns.
Canadian Hospital Specialties Ltd. registered product code LRO with the FDA, listing one product.
Safe Food for Canadians Regulations: Glossary of key terms - inspection.canada.ca
Nipro has received FDA clearance for a new hemodialysis device, enhancing its market position.
Agence canadienne d'inspection des aliments - Canadian Food Inspection Agency
Canada mandates regulatory enrollment for medical devices to ensure compliance in the industry.
The article provides guidance on standards for compliance with Medical Devices Regulations in Canada.
The HydroMARK™ Breast Biopsy Site Marker has been recalled due to safety concerns.
CONMED has expanded AirSeal compatibility to the da Vinci 5 platform, enhancing surgical device integration.
Medical device inspections report card summary - drug-inspections.canada.ca
Update your application (submit new information we didn’t request) - canada.ca
Centrella Bed Frame (2020-05-12) - recalls-rappels.canada.ca
A. AMSORB PLUS PREFILLED G-CAN W TO V (2021-08-04) - recalls-rappels.canada.ca
HydroMARK™ Breast Biopsy Site Marker - recalls-rappels.canada.ca
Guidance on using standards to support compliance with the Medical Devices Regulations - canada.ca
Mandatory use of the regulatory enrolment process for medical devices: Notice to industry - canada.ca