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]

上述产品获得欧盟 MDR 认证，表明其符合欧盟最新医疗器械法规要求，具备欧盟市场的最新准入条 件，可以在相关海外市场合法销售，对公司产品在相应市场的推广和销售起到推动作用。 智通财经APP讯，维力医疗(603309.SH)发布公告，公司近日收到欧盟公告机构通知，公司欧盟医疗器 械法规(Medical Device REGULATION (EU) 2017/745，简称"MDR")认证证书中新增了多个产品的欧盟 MDR 认证。 ...

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]

格隆汇11月5日丨天益医疗(301097.SZ)公布，公司于近日收到欧盟医疗器械法规(Medical Device Regulation (EU) 2017/745，简称"MDR")认证证书。 ...