Company NewsYour current position:Home > News > Company News Hitec Medical MDR training Technical Documentation Requirements under MDR Part 1 Elements Content Device description, included software and accessories General description of the product, including intended use and intended users; Hitec Medical MDR training - Product classification under MDR (Part 2) Rule 10. Diagnostic and testing equipmentEquipment used for lighting (examination lamps, surgical microscopes) Class I;For imaging of radiopharmaceut 2023 Medica Germany 2022 CMEF The 86th CMEF China International Medical Device Expo (hereinafter referred to as "CMEF") was held in Shenzhen, Guangdong Province from 23rd Hitec Medical FDA training FDAs Definition of Medical Devices part 2 FDA’s control over different categories of medical devicesLabel requirements"Registering a factory for a device or obtaining a registration numb KIMES in Seoul Korea Welcome to visit Hitec Medical booth number D255 in COEX Seoul South Korea. Hitec medical, professional manufacturer of Respiratory, Anesthesia a Prev 12345678910 Next