Germany-based Raumedic has obtained 510(k) clearance from the US Food and Drug Administration (FDA) for its NEUROVENT-PTO device, a multimodal catheter for monitoring brain tissue oxygen partial pressure, intracranial pressure (ICP), and ...
Tags: Raumedic, Neurovent-PTO Device
Medical technology company Medtronic has introduced the Export Advance aspiration catheter, a new device to remove coronary thrombus, in the US. Export Advance aspiration catheter has a pre-loaded stylet, which increases the ...
Tags: Medtronic, Aspiration Catheter
Surefire Medical, a developer of infusion systems for the interventional radiology and interventional oncology markets, has introduced Surefire Infusion System mT, designed to treat vessels as small as 2–3.5mm in interventional ...
Israel-based Cardiosonic announced it is currently enrolling patients in the TIVUS II clinical trial, designed to assess the safety, efficacy and performance of its TIVUS system using a next generation multidirectional catheter. TIVUS ...
Tags: Cardiosonic, Clinical Trial
CardioFocus, developer of the HeartLight endoscopic ablation system (EAS) for the treatment of atrial fibrillation (AF), has concluded enrollment of its US pivotal trial evaluating the HeartLight system, for the treatment of symptomatic ...
US-based CardioKinetix has announced the successful treatment of first two Chinese heart failure patients with its Parachute ventricular partitioning device, a minimally invasive treatment for patients with heart failure caused by damage to ...
Tags: CardioKinetix, Partitioning Device
Ireland-based Crospon has obtained an approval from the US Food and Drug Administration for its EsoFLIP balloon dilation catheter. The device allows measurements of lumen diameter to be made electrically and it eliminates the patient's ...
Sotera Wireless, a medical device company, has obtained an approval from the US Food and Drug Administration (FDA) for its continuous non-invasive blood pressure (cNIBP) technology, a new feature of the ViSi Mobile wireless patient ...
Tags: cNIBP Technology, Sotera Wireless
Advanced Catheter Therapies (ACT), a US-based developer of medical devices, has obtained 510(k) approval from the US Food and Drug Administration (FDA) for its Occlusion Perfusion Catheter, designed to temporarily occlude a specific region ...
Tags: ACT, Occlusion Perfusion Catheter
Terumo Interventional Systems, a division of Terumo Medical, has announced the nationwide availability of the detachable AZUR CX peripheral coil system (AZUR CX), designed for endovascular occlusion of peripheral vasculature. It is ...
Tags: Terumo, Peripheral Coil System
Shanghai MicroPort EP MedTech, a wholly-owned subsidiary of Shanghai MicroPort Medical Group, has obtained CE Mark approval for its Columbus 3D EP navigation system, indicated for the diagnosis and treatment of complex arrhythmia diseases. ...
US-based Intact Vascular has completed the patient enrollment in the Tack Optimized Balloon Angioplasty (TOBA) study, a multi-center study designed to collect confirmatory data on the use of Tack-It Endovascular System in the superficial ...
Tags: Medicine, Patient Enrollment
TVA Medical, a medical device company focused on endovascular innovation, has announced that its vascular catheter-based Flex system for hemodialysis access has demonstrated success in the FLEX-1 pilot study. Recently, the company ...
Tags: TVA Medical, Medicine
Medical device company Teleflex has introduced ARROW JACC (jugular axillo-subclavian central catheter), a small-french size antimicrobial and antithrombogenic catheter designed for both acute and long-term use, with Chlorag+ard technology. ...
German-based JenaValve Technology has obtained CE Mark approval for its transapical transcatheter aortic valve implantation (TAVI) system, designed to treat aortic insufficiency (AI). AI, also known as aortic regurgitation, is a condition ...