With the continuous improvement of medical standards, medical devices have been widely used in the fields of disease diagnosis, prevention, monitoring, treatment and rehabilitation. Any medical device that has been approved for marketing is not absolutely safe.
From January 1, 2021, the unique identification of the first batch of medical device products will be officially implemented, marking that the unique device identification (UDI) work has entered the formal implementation stage from the pilot exploration stage and included in the first batch The medical devices in 69 categories of 9 categories in the product catalogue must meet the requirements of UDI regulations.
"The medical robot innovation chain should make up for the shortcomings from technical research to product development, and form a full chain ecology of upstream and downstream collaborative innovation.
On December 18, 2020, the National Medical Products Administration announced that the innovative medical device "Vertebral artery rapamycin eluting stent system" produced by MicroPort Shentong Medical Technology (Shanghai) Co., Ltd. was approved for marketing.
The stapler is a medical device that replaces traditional manual sutures in surgical operations. It is mainly used for cutting, resection, and anastomosis of various cavities and diseased tissues in the human body, as well as the reconstruction of organ functions.