Group 1 - The company has received notification from the EU regulatory body regarding the addition of multiple products to its Medical Device Regulation (MDR) certification [1] - The MDR certification indicates that the products comply with the latest EU medical device regulations, allowing for legal sales in relevant overseas markets [1] - The certification is expected to enhance the promotion and sales of the company's products in the corresponding markets [1] Group 2 - The actual sales performance of the newly certified products in overseas markets will depend on future marketing efforts, and the specific impact on the company's future operating performance remains unpredictable [1]

Core Viewpoint - The company, Weili Medical (603309.SH), has received notification from the EU announcement agency regarding the addition of multiple products to its EU Medical Device Regulation (MDR) certification [1] Group 1 - The newly certified products comply with the latest EU medical device regulations, indicating they meet the current market access requirements in the EU [1] - The EU MDR certification allows the company to legally sell its products in relevant overseas markets, enhancing the promotion and sales of its products in those markets [1]

Core Viewpoint - The company, Weili Medical (603309.SH), has received notification from the EU announcement agency regarding the addition of multiple products to its EU Medical Device Regulation (MDR) certification, indicating compliance with the latest EU medical device regulations and enabling legal sales in relevant overseas markets [1] Group 1 - The company has obtained EU MDR certification for several products, which signifies adherence to the latest EU medical device regulatory requirements [1] - The new certification allows the company to meet the latest market access conditions in the EU, facilitating the promotion and sales of its products in corresponding markets [1]

Core Viewpoint - The company, Weili Medical (603309.SH), has received notification from the EU announcement agency regarding the addition of multiple products to its EU Medical Device Regulation (MDR) certification, indicating compliance with the latest EU medical device regulations and enabling legal sales in relevant overseas markets [1] Group 1 - The company has obtained EU MDR certification for several products, which signifies adherence to the latest EU medical device regulatory requirements [1] - The new certification allows the company to meet the latest market access conditions in the EU, facilitating the promotion and sales of its products in corresponding markets [1]

Core Viewpoint - Tianyi Medical (301097.SZ) has recently received the certification under the European Union Medical Device Regulation (EU MDR 2017/745) [1] Group 1 - The company has achieved a significant regulatory milestone by obtaining the MDR certification, which is crucial for its operations in the European market [1]