Inventek Systems 341 Manuel D’Utilisation

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  When the S2 initially powers on, the screen will illuminate if the battery is installed properly and charged. 

Remove the S2 from service and contact Mortara if the screen does not activate when a new or fully charged 
battery is initially installed. 

 

  Batteries are known to leak their contents when stored for an extended period of time in unused equipment. 

Always remove the battery after completing operating the telemetry device. Always place rechargeable 
batteries in the battery charger when not in use. This ensures that the battery is recharged for the next time the 
telemetry device is operated. 

 

  There is a potential pinch hazard when applying the battery compartment cover to the device that could result in 

minor injury. Care should be taken to avoid entrapment of fingers when performing this operation. 

 

  The S2 is designed to meet applicable specifications when using Mortara-approved patient cables and 

accessories. Use of non-approved cables and accessories may result in reduced performance or electromagnetic 
interference, and may pose possible patient and user safety concerns. 

 

  Do not use excessive force on any of the connection cables and handle all accessories with care. 

 

  Conductive parts of the ECG patient cables, electrodes, and associated connections of type CF applied parts, 

including the neutral conductor of the patient cable and electrode should not come into contact with other 
conductive parts including earth ground. 

 

  To avoid the possibility of serious injury or death during patient defibrillation, do not come into contact with 

telemetry device or patient cables. 

 

  Accessories may be provided with separate user manuals. Read these manuals thoroughly and refer to them for 

specific functions.  It is recommended to keep all manuals together. 

 

  To avoid potential for spread of disease or infection, single-use components and accessories (e.g., electrodes, 

, pouches, etc.) must not be reused. To maintain safety and effectiveness, ECG electrodes and sensors must 
not be used beyond their expiration date or useful life. 

 

  All accessories including cables, connectors and other patient-applied parts supplied with the S2 do NOT 

contain any latex. If the patient develops an allergic reaction or rash, immediately remove the accessory and 
inform Mortara. 

 

  The S2 has not been designed for use together with electrosurgery equipment. 

 

  The S2 is defibrillator protected in compliance with IEC 60601-2-27 standards if used with Mortara-approved 

patient cables. Defibrillation while using non-approved patient cables may damage the device beyond repair 
and cause a safety hazard to the patient. 

 

  Excessive patient movement could interfere with the operation of the system. 

 

  Proper clinical procedure must be employed to prep the electrode and sensor sites, and to monitor the patient for 

excessive skin irritation, inflammation, or other adverse reactions. Electrodes and other sensors that are 
intended for short-term use should be removed from the patient promptly following use.