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2ndLife Checklist:

2nd Life Series

11-Point AED Checklist

  1. AED will be upgraded to current AHA guidelines (if upgrade available from manufacturer) 
  2. Each unit is connected to a new Fluke Impulse 7000 defibrillator analyzer to simulate a shockable rhythm, and 3 shocks are delivered to assure the joule output is within FDA guidelines 
  3. All device and performance information is recorded and stored in both electronic and paper form 
  4. Visual inspection to ensure AED is in acceptable cosmetic condition 
  5. Device is thoroughly and meticulously cleaned (think Q-tips and toothpicks) 
  6. AED is accessorized and made patient-ready with electrodes and batteries installed 
  7. AED is turned on to initiate self-test that assures it is ready to be used in a rescue 
  8. Battery and Pad expiration dates are recorded to ensure you are notified 60 days before your accessories require replacement (end user ultimately responsible for replacement) 
  9. Packing slip is hand ‘checked’ to ensure all items are included 
  10. Order is professionally packed in accordance to Fedex/UPS regulations 
  11. AED tracing is submitted to the manufacture in accordance with FDA regulations

22-Point Defibrillator Checklist

  1. Unit is visually inspected to ensure device is cosmetically acceptable
  2. Software version is recorded
  3. Software is upgraded to latest version (if available from manufacturer)
  4. Time and Date are set
  5. Unit and customer info is entered into Ansur Software and stored in both electronic and paper form
  6. Device is tested on equipment regularly calibrated by the manufacturer
  7. Joule output is tested and recorded at intervals of: 10, 20, 50, 100, 200, 300, 360 (if applicable)
  8. Joule output is recorded and displayed on a sticker placed on the device
  9. Calibration sticker notes “Next Inspection” date according to manufacturer guidelines
  10. Pacing is tested (if applicable)
  11. Spo2 is tested (if applicable)
  12. Non-invasive Blood Pressure is tested (if applicable)
  13. Capnography is tested (if applicable)
  14. Printer is tested, and test strip is shipped with the unit to show functionality
  15. All testing results stored on server in case ever required and test summary is printed and filed
  16. Unit is fully accessorized and assembled patient-ready
  17. Packing slip is printed and hand checked it insure all items are included
  18. Device is thoroughly and meticulously cleaned (think Q-tips and toothpicks)
  19. Device is professionally packed using approved materials and insured
  20. Tracking # is recorded on SO/Invoice 
  21. Battery and Pad expiration dates are recorded to ensure you are notified 60 days before your accessories require replacement (end user ultimately responsible for replacement)
  22. Device information and destination are submitted to the manufacture in accordance with FDA regulations