Datex-Ohmeda Cardiocap™/5

Technical Reference Manual

Document Number M1031914

2nd edition
9 May 2007

Datex-Ohmeda, Inc. GE Healthcare Finland Oy

P.O. Box 7550, Madison Helsinki, Finland
WI 53707-7550, USA P.O. Box 900
Tel. +1-608-221-1551 FI-00031 GE
Fax +1-608-222-9147 Tel. +358 10 39411 Fax +358 9 146 3310
www.gehealthcare.com
Copyright © 2007 General Electric company. All rights reserved.
 Contents

Chapter 1. Overview
1.1 About this manual ................................................................ 1-1
Related documentation ............................................................................... 1-1
1.2 Cardiocap/5 models and features ......................................... 1-2
1.2.1 Options for hemodynamic model (F-MX) ....................................................... 1-2
1.2.2 Options for hemodynamic model with airway gas measurement (F-MXG)......... 1-2
1.2.3 Data collection and management options (for F-MX and F-MXG)..................... 1-2
1.3 Monitor structure ................................................................. 1-3
1.3.1 Measurement parameter units..................................................................... 1-3
NESTPR unit ............................................................................................... 1-3
PVX unit for Patient Spirometry (N-XV option)................................................. 1-4
CAiO unit (N-XC, N-XCO, and N-XCAiO options) .............................................. 1-4
Datex-Ohmeda enhanced pulse oximetry (N-XOSAT option)............................ 1-4
Nellcor® compatible pulse oximetry (N-XNSAT option)................................... 1-4
NeuroMuscular Transmission (N-XNMT option) .............................................. 1-4
1.3.2 Communication.......................................................................................... 1-4
1.3.3 CPU board.................................................................................................. 1-4
Distributed processing................................................................................. 1-5
1.3.4 Display ...................................................................................................... 1-5
1.3.5 I/O board................................................................................................... 1-5
1.3.6 DC/DC board ............................................................................................. 1-5
1.3.7 AC/DC unit................................................................................................. 1-5
1.3.8 Recorder (N-XREC option)............................................................................ 1-5
1.4 Symbol definitions................................................................ 1-6
Symbols on equipment................................................................................ 1-6
Symbols on screens .................................................................................... 1-7
Symbols on transport packaging .................................................................. 1-7
1.5 Safety precautions ............................................................... 1-8
1.5.1 Warnings.................................................................................................... 1-8
Installation ................................................................................................. 1-8
Power connection ....................................................................................... 1-8
External connection..................................................................................... 1-8
Electrical shock hazard ................................................................................ 1-9
Fuse replacement ....................................................................................... 1-9
Explosion hazard......................................................................................... 1-9
Patient safety.............................................................................................. 1-9
Temperature probes .................................................................................... 1-9
Cleaning and service ................................................................................... 1-9
Accessories .............................................................................................. 1-10
1.5.2 Cautions .................................................................................................. 1-10
General .................................................................................................... 1-10
Installation ............................................................................................... 1-10
Before use................................................................................................ 1-10
Cardiocap/5 Technical Reference Manual

Airway gas measurement ...........................................................................1-10

Autoclaving and sterilizing..........................................................................1-10
Cleaning and service .................................................................................1-10
Batteries...................................................................................................1-11
Special components and modifications ......................................................1-11
Storage and transport................................................................................1-11
1.5.3 ESD precautionary procedures ...................................................................1-11
ESD precautionary procedure training .........................................................1-12
1.5.4 Disposal...................................................................................................1-12
1.5.5 Points to note ...........................................................................................1-12
1.6 Specifications.................................................................... 1-12
1.6.1 F-MX and F-MXG frames ............................................................................1-12
Power supply ............................................................................................1-12
Environmental conditions...........................................................................1-12
Mechanics................................................................................................1-13
LCD display...............................................................................................1-13
Battery .....................................................................................................1-13
1.6.2 NIBP ........................................................................................................1-13
1.6.3 Temperature .............................................................................................1-13
1.6.4 ECG .........................................................................................................1-13
1.6.5 Impedance respiration ..............................................................................1-14
1.6.6 Pulse oximetry, standard............................................................................1-14
1.7 Specifications for options ................................................... 1-14
1.7.1 Classifications ..........................................................................................1-14
According to IEC 60601-1 .........................................................................1-14
Classification according to EU Medical Device Directive ...............................1-15
1.7.2 Pulse oximetry, Datex-Ohmeda enhanced (N-XOSAT) ...................................1-15
1.7.3 Pulse oximetry, Nellcor compatible (N-XNSAT) .............................................1-16
1.7.4 Invasive blood pressure (N-XP) ...................................................................1-16
1.7.5 Airway gases (N-XC, N-XCO, and N-XCAiO)...................................................1-16
General ....................................................................................................1-16
Respiration rate (RR)..................................................................................1-17
Carbon Dioxide (CO2), Oxygen (O2), and Nitrous Oxide (N2O) .........................1-17
Anesthetic agents (AA)...............................................................................1-17
Agent identification ...................................................................................1-17
MAC .........................................................................................................1-18
Normal conditions .....................................................................................1-18
Conditions exceeding normal .....................................................................1-18
1.7.6 Patient Spirometry (N-XV) ..........................................................................1-19
Conditions exceeding normal .....................................................................1-20
1.7.7 NeuroMuscular Transmission (N-XNMT).......................................................1-20
NMT stimulation modes .............................................................................1-20
Stimulator.................................................................................................1-21
Regional block mode .................................................................................1-21
1.7.8 Recorder (N-XREC) ....................................................................................1-21
 Contents

Table of Figures
Figure 1-1. Cardiocap/5 monitor structure........................................................................ 1-3