近日，FDA将Medline Industries旗下的数百万支Namic血管造影旋转接头控制注射器界定为一级召回。据悉，Medline曾于今年2月对该产品发起主动召回；4月9日，FDA发布警告信并表示将采取“监管行动”，召回涉及超过400万支注射器和超过100万套包含注射器的手术套件。
近日，中国科学院院士、院长王建安教授带领团队，在浙江大学医学院附属第二医院运用医院主导自主研发的经导管二尖瓣置换系统，成功为71岁高危患者完成微创“心门”置换，打响了这款国产器械全国注册临床试验的第一枪。
In the USA and China, 30% of severe symptomatic aortic stenosis patients are inoperable. This is due to other health risks or old age. For inoperable patients, minimally invasive valve repair or replacement via a transcatheter approach is recommended.
北京大学第一医院泌尿外科科主任李学松教授团队成功运用国产康多手术机器人，为一名复杂上尿路梗阻患者实施完全体内自体肾移植术
Shanghai has become the first place in China to move toward an official licensing system for doctors performing robot-assisted surgery.
2026年3月12日，金仕生物自主研发的 ProStyle M® 经导管二尖瓣瓣膜系统（以下简称“ProStyle M®”） 在纯超声引导下顺利完成确证性临床研究首例植入。
Addressing key clinical challenges: Adopting an eccentric structural design to reduce the difficulty of surgical operation and the risk of left ventricular outflow tract obstruction, while achieving stable anchoring performance and good hemodynamic performance.
Following its successful application in Greece, HugeMed 6.3Fr Single-Use Ureterorenoscope is rapidly gaining recognition globally, with more medical institutions adopting it for its precision and patient-centric benefits.
The system allows surgeons to construct customized solutions for each patient’s specific needs.
Highridge Medical secured exclusive U.S. distribution rights for PathKeeper's Navigation System, expanding its spine technology portfolio with radiation-free, AI-enhanced surgical navigation.
