Physio Control LIFEPAK 9 - Page 60

Testing 3
Table 3-1 PIP Test Equipment (cont.)
Equipment Specifications Manufacturer
Patient Cable 3-lead, AHA or Physio-Control PN 9-10418-02
3-lead, IEC Physio-Control PN 800947-01
Recorder paper SOmm (use only Physio-Control pa- Physio-Control PN 804700
Metric ruler or
recorder paper
per)
Resolution: 1mm divisions
Timer
1 second resolution Aristo or equivalent
*Equivalent equipment is required to meet the specifications listed in the specifications column.
Caution Possible Equipment Damage. Be sure to use only recorder paper from
Physio-Control (PN 804700). Other paper may damage the printhead and
may not print legibly.
PIP-Test Equipment All test equipment used in performing the PIP must have a current calibration
Verification label affixed to its exterior. The calibration label must be issued by a
certified calibration facility.
PIP-Workstation The ac line power for this workstation must be connected to a grounded
PIP-Personnel
power source.
Personnel performing this PIP must be thoroughly familiar with the operation
of the LIFEPAK 9 defibrillator/monitor. In addition, personnel performing
this PIP must meet at least one of the following levels of education or
experience:
e Associate of applied science degree with a major emphasis in
biomedical electronics
e Certificate of technical training in electronics with a major emphasis in
biomedical electronics
e Equivalent biomedical electronics experience.
Warning
SHOCK HAZARD. When charged and discharged during this PIP, the
LIFEPAK 9 defibrillator/monitor discharges up to 360J of electrical energy
through the defibrillator paddles. Unless discharged properly as described
in this PIP, this electrical energy may cause injury or death. Do not
attempt to perform this procedure unless you are thoroughly familiar with
the operation of the LIFEPAK 9 defibrillator/monitor.
170008-000 A
© August 1993 Physio-Control
All Rights Reserved 3-3