广州维力医疗器械股份有限公司关于公司产品获得欧盟MDR认证的公告

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]