IVUS-CTO: Comparison of the Effect of Intravascular Ultrasound-guided Versus Angiographic-guided Drug-eluting Stent Implantation on Long-term Clinical Outcomes in Patients With Chronic Complete Occlusion of Coronary Artery Disease: a Prospective, Multicenter, Randomized Controlled Clinical Study
This study aims to evaluate the treatment of Chronic total occlusion (CTO) disease. Whether Intravascular Ultrasonography (IVUS) guiding the implantation of drug-eluting stents (DES) will provide better long-term clinical outcomes compared with conventional angiography
A Post-Approval Study of the RotablatorTM Rotational Atherectomy System in China
Rotational atherectomy (RA) facilitates percutaneous coronary intervention for complex de novo lesions with severe calcification. Some observational studies and a small randomized trial indicated that a strategy of routine RA did not conferred reduction in restenosis or MACE, but these studies are limited by missing follow-up, insufficient power to compare outcomes, and confounding factors in the RA group (long lesion length, etc.). With recent developments in medical therapy, advances in design and delivery of drug-eluting stents (DES), and advances in noninvasive and intravascular coronary imaging, the use of RA in current real-world practice remains to be well determined. We aimed to compile real-world clinical outcomes data for the RotablatorTM Rotational Atherectomy System in routine clinical practice in China.
Registry of Bronchial Thermoplasty (BT) Procedures in China
The objective of this Registry is to collect real-world outcome data for bronchial thermoplasty (BT) procedures in patients with severe persistent asthma who remain symptomatic despite taking standard of care maintenance medications.
100 项与 波科国际医疗贸易(上海)有限公司 相关的临床结果
0 项与 波科国际医疗贸易(上海)有限公司 相关的专利(医药)
波科国际医疗贸易(上海)有限公司报告,由于更新说明书的原因,生产商波士顿科学公司Boston Scientific Corporation对其生产的经导管植入式主动脉瓣膜ACURATE neo2? Aortic Valve(国械注进20243130406)、经导管植入式主动脉瓣膜输送导管ACURATE neo2? Transfemoral Delivery System(国械注进20243030548)主动召回。召回级别为三级召回。涉及产品的型号、规格及批次等详细信息见《医疗器械召回事件报告表》。 附件:医疗器械召回事件报告表 2024年11月15日波科国际医疗贸易(上海)有限公司召回报表.pdf
波科国际医疗贸易(上海)有限公司报告,由于手柄和产品远端之间切割丝的封闭部分存在异物等原因,生产商波士顿科学公司Boston Scientific Corporation对其生产的一次性使用括约肌切开刀Cannulating Sphincterotome(国械注进20173010673)主动召回。召回级别为二级召回。本次召回涉及的产品未进口至中国,具体型号、规格及批次等详细信息见《医疗器械召回事件报告表》。 附件:医疗器械召回事件报告表 2024年6月27日波科国际医疗贸易(上海)有限公司.pdf
波科国际医疗贸易(上海)有限公司报告,由于微导管接口的工作通道中存在粘合剂,可能会导致粘性颗粒进入患者血液,波士顿科学公司Boston Scientific Corporation对其生产的可扭转微导管Direxion Torqueable Microcatheter and Direxion HI-FLO Torqueable Microcatheter(国械注进20163030159)进行主动召回。召回级别为二级召回。涉及产品的型号、规格及批次等详细信息见《医疗器械召回事件报告表》。 附件:医疗器械召回事件报告表 2024年6月14日波科国际医疗贸易(上海)有限公司召回报表.pdf
100 项与 波科国际医疗贸易(上海)有限公司 相关的药物交易
100 项与 波科国际医疗贸易(上海)有限公司 相关的转化医学