Paulette announced that the company recently obtained a Class III medical device registration certificate issued by the State Drug Administration. The product is a G series patient monitor. The registration certificate number is Guozheng No. 20263072105, which is valid until October 8, 2031. The product can be applied to multiple scenarios such as operating rooms and intensive care rooms. In addition to the six standard monitoring parameters, it can expand multiple specialized modules to meet diverse monitoring needs. This certification has enriched the company's monitor product matrix, helped expand the customer base and enhance the company's overall competitiveness in the field of life information and support. The actual sales situation of the product depends on future market demand and promotion results, and it is not yet possible to accurately predict its impact on future revenue.

Disclaimer:Webull uses external vendor Google Translation Service for news translations where we endeavour to ensure these are correct, however, we recommend that you please double-check this information accordingly. Webull is not responsible for translation errors or issues.