Manufacturers selling Class II, III and IV medical devices in Canada are required to have the medical device license. The MDL process is comparable to the FDA 510(k) process in the United States, according to the report.
More articles on gastroenterology:
Does sigmoidoscopy fill a colorectal cancer screening niche?
19 things to know about GI compensation & satisfaction in 2014
AGA releases new tool for Crohn’s disease treatment
At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.
