The NANOSTIM wireless pacemaker is indicated for: 1. Chronic atrial fibrillation with second-degree AV block or bifascicular branch block. 2. Inaugural rhythms with second or third degree AV block or branch block and a low level of physical activity or a low expected life expectancy. 3. Sinus bradycardia with pausasaislated or unexplained syncope with electrophysiological results. Uses: the wireless pacemaker NANOSTIM is a pulse generator designed for bradycardia stimulation that incorporates a battery and electrodes and must be implanted in the right ventricle. Since it is a cordless device, it does not need a connector, stimulation cable or pulse generator pocket. A non-retractable distal helix with a single twist fixes the device to the endocardium. In addition, three sutures in the outer part of the head of the device offer a secondary fixation. Detection and stimulation occur between a distal electrode near the helix and the external housing of the device. The proximal end of the device has a mechanism that allows coupling it to the decolocation and extraction catheters for repositioning and extraction. The device is communicated bidirectionally with the programmer by electrical signals that are processed between the electrodes of the implanted device and the skin electrodes attached to the patient's chest and connected to the programmer. Accordingly, the device transmits signals by circuits and electrodes previously designed for stimulation, with data encoded by pulses during the refractory period of the heart. The device detects the blood temperature of the right ventricle and increases the frequency of stimulation as the metabolic requirement increases.
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.
Neurostimulation system GENESIS: is indicated as an aid in the treatment of chronic pain, not treatable with other therapies of the trunk or extremities including unilateral or bilateral pain associated with any of the following cases: back surgery failure syndrome, as well as low back pain in lower extremities of difficultness. EON / EON MINI neurostimulation system: there are indicated extremities, including unilateral or bilateral pain associated with some of the following cases; syndrome of failure of back surgery, as well as lower back pain and pain in difficult extremities.System MULTIPROGRAM TRIAL STIMULATOR: used for the stimulation of the spinal cord (eme) in the treatment of chronic pain deltronco and extremities, either as an individual palliative method or other types of treatment in the case of multidisciplinary therapy. This modular stimulation system is indicated as an adjuvant in the treatment of chronic refractory pain of the trunk and extremities, including unilateral or bilateral pain associated with angina and chest pain. peripheral vascular disease. Addition of indications for use: "PRODIGY MRI implantable implant model 3772 and PENTA 3228 and OCTRODE 3186 electrodes are conditional magnetic resonance.The use of these devices is conditionally safe in the MRI environment (magnetic resonance imaging) if a complete MRI system is used. and according to the instructions