ZOLL R Series Monitor Defibrillator Rev J User Manual
Page 167
9650-0904-01 Rev. K
ZOLL R Series Operator’s Guide
i
Table of Contents
Chapter 1
General Information
Product Description ............................................................................................................ 1-1
R Series Model Features .................................................................................................... 1-3
How to Use This Manual..................................................................................................... 1-4
Operator’s Guide Updates .................................................................................................. 1-4
Unpacking ........................................................................................................................... 1-4
Symbols Used on the Equipment ....................................................................................... 1-4
Conventions ........................................................................................................................ 1-7
Defibrillator Function ........................................................................................................... 1-7
Intended Use — Manual Operation ............................................................................ 1-8
Intended Use — Semiautomatic Operation (AED) ..................................................... 1-8
Intended Use — ECG Monitoring ............................................................................... 1-8
Intended Use — Real CPR Help ................................................................................ 1-9
Semiautomatic Operation Contraindications for Use .................................................. 1-9
Defibrillator Complications .......................................................................................... 1-9
Defibrillator Output Energy ......................................................................................... 1-9
External Pacemaker (Optional)........................................................................................... 1-9
Intended Use — Pacemaker ..................................................................................... 1-10
Pacemaker Complications ........................................................................................ 1-11
Pediatric Pacing ........................................................................................................ 1-11
Intended Use — SpO
2
Monitoring .................................................................................... 1-11
Intended Use — EtCO
2
Monitoring................................................................................... 1-12
Intended Use — NIBP ...................................................................................................... 1-12
ECG Monitoring ................................................................................................................ 1-13
Recorder Function (Manual Mode Only)........................................................................... 1-13
Paddles and Electrodes .................................................................................................... 1-13
Batteries............................................................................................................................ 1-14
Code-Ready System......................................................................................................... 1-15
Safety Considerations....................................................................................................... 1-15
Warnings........................................................................................................................... 1-15
Operator Safety ........................................................................................................ 1-17
Patient Safety ........................................................................................................... 1-18
Cautions............................................................................................................................ 1-19
Restarting the Defibrillator ................................................................................................ 1-20
FDA Tracking Requirements............................................................................................. 1-20
Notification of Adverse Events .................................................................................. 1-21
Software License .............................................................................................................. 1-21
Service .............................................................................................................................. 1-22
The ZOLL Serial Number.................................................................................................. 1-23