9650-0904-01 Rev. N 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.......................................................................................................1-13
ECG Monitoring ................................................................................................................ 1-13
Recorder Function (Manual Mode Only)...........................................................................1-13
Paddles and Electrodes.................................................................................................... 1-14
Batteries............................................................................................................................1-14
Code-Ready System......................................................................................................... 1-15
Safety Considerations....................................................................................................... 1-15
Warnings........................................................................................................................... 1-16
Operator Safety ........................................................................................................1-18
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
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