Core Viewpoint - Shanghai Sanyou Medical Equipment Co., Ltd. has received approval from the National Medical Products Administration for the JAZZ System spinal internal fixation connector system, marking a significant step in the company's internationalization strategy and enhancing its competitive advantage in the spinal product market [1][3]. Medical Device Registration Details - Product Name: Spinal Internal Fixation Connector System JAZZ System [1] - Registration Number: National Medical Device Registration No. 20253130302 [1] - Registrant: Implanet Company [1] - Agent: Shanghai Sanyou Medical Equipment Co., Ltd. [1] - Applicable Scope: The system is suitable for spinal posterior fixation surgery for thoracolumbar (T1-L5) segments, providing binding fixation for segments unsuitable for pedicle screws [1]. - Registration Validity: From July 10, 2025, to July 9, 2030 [2]. - Composition: The system consists of straps and connectors, sterilized by irradiation with a shelf life of 5 years [2]. Impact on the Company - The introduction of Implanet's advanced JAZZ series products enriches the company's non-fusion spinal product line and enhances its competitive advantage [3]. - The product complements the company's innovative spinal fixation systems, providing a more comprehensive and advanced treatment solution for clinical doctors [3]. - This move is a crucial part of the company's international strategy, successfully bringing Implanet's JAZZ series products to the domestic market, thereby strengthening its market competitiveness and overall strength [3].
证券代码：688085 证券简称：三友医疗 公告编号：2025-052