Arab Health

Hitec Medical MDR training Technical Documentation Requirements under MDR Part 2

linical evaluation requirements under MDRClinical evaluation: Clinical evaluation is the collection, evaluation, and analysis of clinical data throu

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