US-based Maquet Medical Systems has obtained 510(k) approval from the US Food and Drug Administration (FDA) for the VOLISTA surgical lighting system. Incorporating Maquet Medical Systems' Luminance Management Device (LMD) technology, the ...
Tags: Surgical Lighting System
MAQUET Medical Systems USA yesterday launched its LED concealed lighting system for the Labor, Delivery and Recovery (LDR) room. The retractable LED light sets a new standard in illumination quality, comfort and operational efficiency ...
Maquet Cardiovascular has obtained CE mark approval for its new Intergard Synergy antimicrobial vascular graft. The Intergard Synergy graft releases broad spectrum antimicrobial agents including silver acetate and triclosan from its ...
Tags: Maquet Cardiovascular, approval, antimicrobial vascular graft
Maquet Cardiovascular, a subsidiary of Swedish Getinge Group, has reported positive results from IABP- SHOCK II trial of its intra-aortic balloon counterpulsation (IABC) therapy, designed to reduce the workload of the heart and improve ...
Tags: IABC, percutaneous coronary intervention, AMI, Maquet Cardiovascular
Maquet Cardiovascular has gained US and European marketing rights for its new SENSATION PLUS 7.5Fr. 40Cc intra-aortic balloon (IAB) catheter, following the US Food and Drug Administration (FDA) and CE mark approvals respectively. The ...
Tags: marketing rights, catheter, FDA
Klenk Holz is launching a new search for investors and has taken Dr Hans Peter Dohmen, the new chief restructuring officer (CRO), on board for this purpose. The declared aim of the procedure is to find a buyer in the framework of a share ...
Tags: market view, wood
Maquet Cardiopulmonary, a unit of Maquet Cardiovascular, has entered into an agreement to purchase Avalon Laboratories' Elite Bi-Caval Dual Lumen Catheter and complimentary vascular access kits for use during extracorporeal life support ...
Tags: Maquet, cardiopulmonary, ECLS