Catheters for coronary dilatation are used for: 1. Balloon dilatation of the stenotic portion of a coronary artery from the stenosis of a bypass graft in order to improve myocardial perfusion. 2. Balloon dilatation of an occlusion in a coronary artery, in order to restore coronary flow in cases of myocardial infarction with ST-segment elevation. 3. Dilation with balloon of a stent after implanting it (balloon models from 2.00 mm to 5.00 mm only).
Designed to administer ventricular stimulation and ventricular defibrillation for the automatic treatment of ventricular arrhythmias that endanger the life of the patient.
Designed to administer ventricular antitachycardia and ventricular defibrillation for the automatic treatment of ventricular arrhythmias that endanger the life of the patient.
It is a rotational left ventricular axial flow assist system and can generate flows of up to 10 liters per minute (LPM) attached to the apex of the left ventricle and the ascending aorta, blood labomba HEARMATE II diverts the blood from the weakened left ventricle and pushes it towards the rest of the body. The controller of the system, through its internal software program regulates the pumping.
Used in the minimally invasive treatment of pathologies of the thoracic aorta, the ZENITH ALPHA thoracic stent is indicated for the treatment of patients with lesions isolated from the descending aortathoracic (excluding dissections), whose vascular anatomical configuration is suitable for endovascular repair, including: anatomical iliac / femorala adequate for access with the required introduction systems non-aneurysmal aortic segments (fixation sites) proximal and distal with respect to the thoracic lesion: with a minimum length of 20mm, and with a mean external wall diameter exterior wall not exceeding 42mm and not less than 15mm.
Indicated as a monitoring platform that indicates the intermittent and continuous hemodynamic measurements related to the evaluation of the essential components of the oxygen supply, as well as the equilibrium between the carrier and the oxygen consumption. The system helps evaluate the patient's condition and supports their clinical decisions related to the optimization of oxygen supply through the control of preload, afterload and contractility. It allows the evaluation of extravascular lung water.
The TRELLIS peripheral infusion system is designed for the controlled and selective infusion of liquids, includingtrolyolitics, inside the peripheral vasculature.
Hydrophilic microguide mod X-CELERATOR 0.010 "300cm, Hydrophilic microguide mod X-CELERATOR 0.014" 300cm, || MARATHON 1.5F / 2.7F microcatheter 165cm guide 0.010 "|| 25cm, ALLIGATOR recovery system 2mm 175cm || OD 0.40mm, ALLIGATOR recovery system 3mm || 175cm OD 0.40mm, ALLIGATOR RETRIEVALDEVICE. 4mm, || all batches with Expiration date between June 2017 and || August 2019.
They are designed to repair or replace the peripheral arteries. ORIGIN is double lumen vascular access catheters are indicated for use as a single cannula for both venous drainage and arterial re-infusion of blood into the internal jugular vein during vitalextracorporeal support procedures (ECLS or ECMO).
This equipment is indicated to be used in the patient in cardiopulmonary arrest. The patient must be unconscious, without spontaneous breathing, without signs of circulation (no pulse). It can be used additionally as a cardioverter / defibrillator according to medical criteria depending on the cardiac arrhythmia that the patient presents.
Recognized method of terminating certain life-threatening arrhythmias, such as ventricular fibrillation and symptomatic tachycardia-ventricular. Provides stimulation to the heart for the automatic treatment of ventricular arrhythmias that endanger the patient's life and when they exhibit symptoms of sudden cardiac arrest.