MDALL (Medical Device Active License Listing) is Health Canada’s official database that lists all licensed medical devices authorized for sale in Canada. It helps verify whether a device meets Canadian safety, quality, and regulatory standards. For manufacturers, having a product listed in MDALL confirms compliance and builds trust with healthcare providers, distributors, and consumers. The listing process involves classifying the device, submitting required technical documentation, paying applicable fees, and undergoing Health Canada’s regulatory review. Once approved, the device is added to MDALL, making it legal to market across Canada.