Pacemaker

  • Model / Serial
  • Product Description
    Pacemaker.Reply and Esprit models that have been interrogated with programmer containing software version 2.24.Manufactured by Sorin CRM.Model   Serial number configuration (where x is any alphanumeric character)         Reply DR   8xxZKxxx   9xxZKxxx   0xxZKxxx Reply D   8xxZLxxx   9xxZLxxx   0xxZLxxx Reply VDR   8xxZMxxx   9xxZMxxx   0xxZMxxx Reply SR   8xxZNxxx   9xxZNxxx   0xxZNxxx Esprit DR   8xxZPxxx   9xxZPxxx   0xxZPxxx Esprit D   8xxZRxxx   9xxZRxxx   0xxZRxxx Esprit SR   8xxZSxxx   9xxZSxxx   0xxZSxxx Esprit S   8xxZTxxx   9xxZTxxx   0xxZTxxx
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Ms Chantal Cadiou Sorin Group France Tel: +33 146013687 Fax: +33 149655451Email: Chantal.cadiou@sorin.com
  • Manufacturer Parent Company (2017)
  • Source
    MHRA

291 devices with a similar name

Learn more about the data here

  • Model / Serial
    NANOSTIM S1DLCP, specific serials.
  • Product Description
    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.
  • Manufacturer
  • Model / Serial
  • Product Description
    Indicated for patients with symptomatic congestive heart failure, including left ventricular dysfunction and a wide range of QRS, as well as one or more of the following conditions: - paroxysmal or permanent symptomatic second and third degree AV block. -blocking of bilateral symptomatic branch. - dysfunction of the paroxysmal or transient sinus-synomatic node with or without associated AV conduction disorder (eg sinus bradycardia, sinus arrest, neuroauricular block (SA) - bradycardia - tachycardia syndrome, to prevent symptomatic bradycardia or certain forms of symptomatic tachyarrhythmias.
  • Manufacturer
  • Model / Serial
  • Product Description
    These defibrillators for cardiac resynchronization therapy (CRT-D) are indicated for patients who are at risk of suffering a cardiac death due to ventricular arrhythmias and heart failure, including ischemic heart failure (NYHA class I), with ventricular dyssynchrony. CRT-D are also indicated to provide ventricular tachycardia and ventricular defibrillation for the automated treatment of life-threatening ventricular arrhythmias.
  • Manufacturer
286 more