Canada
Intelligence de marché des dispositifs médicaux pour Canada. Changements réglementaires, concurrents et tendances d'achats.
Signaux des 7 derniers jours
Bolle (Canada) Inc has registered with the FDA under product code HQY.
The Micra MC1VR01 device has been recalled due to safety concerns.
Micra MC1VR01 (2019-08-06) - recalls-rappels.canada.ca
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
Who is eligible - Disability tax credit (DTC) - canada.ca
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