biosense webster carto 3 manual

that the patient has been moved and prompts to rebuild the map. System configuration must meet the requirements of the IEC 60601-1-1, safety standard for medical electrical systems. According to BWI, CARTO 3 is deployed across the healthcare and public health sector. for Use (IFU) to obtain information relevant to that specific catheter. As in all mapping procedures, ensure that the location reference does, not move during the study. 130 Seiten. The chart lists the minimum distance. CARTO 3 advanced 3D mapping system, integration, scalability and insights for electrophysiology diagnosis and treatment. Current. Biosense Webster Inc. to service the CARTO® 3 System. This equipment should be connected to the common protective ground, The ECG patient cable and the patch cable supplied by Biosense, Webster are designed to be defibrillation proof in accordance with, IEC 60601-2-27 and tested to comply with all applicable regulatory, standards. findings. CARTO® THERMOCOOL® Bi-Directional Catheter. For protection against electrical shock, the PIU power supply unit is, provided with double isolation. This manual provides information on the following topics: • Disconnecting/reconnecting system components when necessary • Relevant service information and issues • Troubleshooting tips and procedures for the CARTO® 3 System. For, example, "Press " means "Press the Ctrl button on the keyboard. of all labeled equipment with this label. Instructions for accessing shortcut menus are written as follows: "Right-click and select xxx", where xxx is the command option in the, Instructions for accessing a particular command on a toolbar are, written as follows: "Click X on the Standard toolbar", where X is a, System Setup Standards ..................................................................................... 6, Patient Indications ............................................................................................ 6, Qualified Users and Training ............................................................................. 6, Warnings ........................................................................................................... 7, General ...................................................................................................... 7, Preventing Fire, Explosion, and Electrical Shock ....................................... 8, Defibrillation ............................................................................................. 9, Location ................................................................................................... 10, CARTOSOUND™ Module ........................................................................... 11, Equipment ............................................................................................... 12, Annual Service Activity ................................................................................... 13, Electromagnetic Compatibility (EMC) ............................................................ 13, Legend to Accompanying Labels ..................................................................... 15, This chapter provides important information regarding the safe function of, • Failure to observe the guidelines and instructions, provided in this chapter could result in faulty, • Physicians may use the CARTO 3 System on patients only.

Electromagnetic propagation is affected by absorption and. Do not use a cellular telephone inside the EP room during a CARTO® 3, Use only parts and accessories manufactured or recommended by, Biosense Webster. Table 4 displays the symbols used on the system hardware and in the. The system can be used on patients who are, eligible for a conventional electrophysiological procedure. The affected product, the CARTO 3 V4 System, is an imaging device that uses electromagnetic technology to create real-time three-dimensional (3D) maps of a patient’s cardiac structures. Biosense Webster Inc. to service the CARTO® 3 System. In such cases, contact the fluoroscopic system supplier to. When the magnets are in the Reduced or Applied. Unauthorized software should not be installed on the system.

documentation supplied with each software module. IRVINE, CA – August 27, 2020 – Johnson & Johnson Medical Devices Companies* today announced the launch of Biosense Webster, Inc.’s CARTO ® 3 System Version 7 and the CARTO PRIME ® Mapping Module. positions, ultrasound imaging is limited only to viewing.

-, Suchen Sie unter 132.682 medizinischen Ausstattungen, CARTO® THERMOCOOL® Bi-Directional Catheter, QWIKSTAR DS 7F 26-pole with 8 mm Tip/Thermocouple, QWIKSTAR 7F 26-pole with 4 mm Tip/Thermocouple, 7F Quadrapolar Catheter with 8 mm Tip/Thermocouple, 6F Quadrapolar Pediatric Catheter with Non-Braided Tip/Thermocouple, 6F Quadrapolar Pediatric Catheter with Non-Braided Tip/Thermistor, Wittkampf (Posterioseptal) Catheter/Thermocouple, Wittkampf (Posterioseptal) Catheter/Thermistor, 7F and 8F Quadrapolar Catheter with 4 and 5 mm Long Reach Braided Tip/Thermocouple, 7F and 8F Quadrapolar Catheter with 4 and 5 mm Long Reach Braided Tip/Thermistor, 7F and 8F Quadrapolar Catheter with 5 mm Braided Tip/Thermocouple, 7F and 8F Quadrapolar Catheter with 5 mm Braided Tip/Thermistor, 7F and 8F Quadrapolar Catheter with 4 mm Braided Tip/Thermocouple, 7F and 8F Quadrapolar Catheter with 4 mm Braided Tip/Thermistor, 6F and 7F Quadrapolar Catheter with Non-Braided Tip/Thermocouple, 6F and 7F Quadrapolar Catheter with Non-Braided Tip/Thermistor, CELSIUS THERMOCOOL Irrigated Tip Catheter, NAVISTAR THERMOCOOL Irrigated Tip Catheter, QWIKCABLE Autoclavable Cable for Diagnostic Catheters with Redel Connector (RT), WEBSTER 4F, 5F, and 6F Hexapolar Pediatric Catheter, WEBSTER Compli Soft Tip Quadrapolar Catheter, WEBSTER Deflectable Octapolar Pediatric Catheter with Redel Connector for His Application, WEBSTER 5F and 6F Quadrapolar Pediatric Catheter, WEBSTER 5F Deflectable Bipolar Pediatric Catheter, CELSIUS® DS Temperature Sensing Ablation Catheters 7F Quadrapolar with 8mm Tip/Thermocouple, CARTOSound Image Integration Module with SOUNDSTAR Catheter, CARTO RMT Electroanatomical Navigation System Brochure, QWIKSTAR DS Navigation and Ablation Catheters, QWIKSTAR Navigation and Ablation Catheters, NAVISTAR THERMOCOOL? When the interference is major, a warning will be generated. your software; functionality, however, is the same. The system has, Physicians and medical staff designated to be CARTO® 3 System users must. holding down the previous key, press the next key."

THERMOCOOL® SMARTTOUCH® Catheter. incorrect target for ablation or perforation.

medical practices regarding patient care and safety should also be considered. Keep this manual available when making requests regarding service, as you It might be necessary to take mitigation, measures, such as re-orienting or relocating the CARTO® 3, Table 2: Guidance and Manufacturer’s Declaration — Electromagnetic, below. When, the relative position between the patches changes, the system warns.

All pictures of maps and signals used in this manual are computer simulations, Some pictures may differ slightly from the ones actually appearing in. About Biosense Webster’s CARTO ® 3 System The CARTO ® 3 System is an advanced imaging technology that utilizes electromagnetic technology to create real-time 3D maps of a patient’s cardiac structures. These types of notes provide examples, to help clarify. CARTO System, CARTO Smarttouch, Biosense Webster, Inc. Only licensed medical practitioners who have completed the. As soon as the disturbance ends, this, error disappears. 3 Seiten.

Es handelt sich um unverbindliche Preisangaben, die sich je nach Land, Rohmaterialkursen und Währungsvariationen ändern können. the customer’s site during the warranty period. allowable between the image intensifier and the patient table. * Die Preise verstehen sich ohne Lieferkosten und Zollgebühren und enthalten keine der Zusatzkosten, die aus Installationsoptionen oder Inbetriebnahme resultieren. include contours, and subsequent misinterpretation of contour maps. The CARTO® 3 System Location Technology is based on body, coordinates defined by three back patches. Failure to do so might result in incorrect placement of the, Color interpolation of electrical information between two relatively, distant images (ultrasound and CARTO® 3 System) can lead to user, misinterpretation of data when registering the two images.

Normal operation of a pacemaker is not, Verify the ICD programming after completing the CARTO® 3, The CARTO® 3 System might interfere with fluoroscopy systems that, use magnetic field based proximity sensors or with digital fluoroscopic, systems. The, "immediate vicinity" is within 5 cm of the catheter tip for, instruments the size of those used in the operation room (such as, scissors, scalpels, ECG nipples, other catheter electrodes, and, pacemakers). By refining the MEM experience, the CONFIDENSE ™ Module introduces a new degree of control over point acquisition and insight into your mapping procedures. after completing the CARTO® 3 System training course. Warranty compliance requires fulfilling all the above conditions. CARTO® 3 System training course may use the system. Installation and testing of the equipment should be performed. All menu options and fields that appear on the screen are in smaller, sized boldface Arial font. complete the training course prior to using the system. CARTO PRIME ® Mapping Module offers a suite of tools that may help to shorten ablation time 1. Parts and accessories used must meet the. may be referred to some of the information supplied herein. damage to the collected data or equipment.

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