Operator's Manual Part 1
Table Of Contents
- Contents
- 1 The Basics 1-1
- 2 Safety 2-1
- 3 Equipment Overview 3-1
- Introduction 3-3
- ApexPro Telemetry System 3-4
- Compatibility with Bedside Monitors 3-5
- ApexPro Transmitters 3-6
- ApexPro CH Transmitter (not for sale outside of the U.S. and Canada) 3-10
- ApexPro FH Transceiver (not for sale outside of the U.S.) 3-11
- Apex Oximeter SpO2 Module 3-12
- Xpod™ Oximeter 3-13
- Accutracker DX Noninvasive Blood Pressure (NBP) Monitor 3-14
- DINAMAP® PRO Series Monitors 3-16
- Antenna System 3-17
- Receiver System 3-17
- Unity Network 3-17
- CIC Pro Clinical Information Center 3-18
- 4 Connection 4-1
- 5 Maintenance 5-1
- 6 Telemetry Setup 6-1
- 7 Admit/View a Patient 7-1
- 8 Alarm Control 8-1
- 9 Printing 9-1
- 10 Patient Data 10-1
- 11 ECG Monitoring 11-1
- 12 SpO2 Monitoring 12-1
- 13 NBP Monitoring 13-1
- Introduction 13-3
- Safety Considerations 13-4
- Programming the Blood Pressure Monitor 13-5
- Patient Preparation 13-9
- NBP Monitoring 13-13
- Pressures Tab Sheet 13-15
- Troubleshooting 13-17
- Message Glossary A-3
- Contact Information B-3
- Abbreviations and Symbols C-3
- The Basics D-3
- Safety D-5
- Equipment Overview D-8
- Connections D-14
- Maintenance D-18
- Compliance D-26
- 1 The Basics
- 2 Safety
- 3 Equipment Overview
- Introduction
- ApexPro Telemetry System
- Compatibility with Bedside Monitors
- ApexPro Transmitters
- ApexPro CH Transmitter (not for sale outside of the U.S. and Canada)
- ApexPro FH Transceiver (not for sale outside of the U.S.)
- Apex Oximeter SpO2 Module
- Xpod™ Oximeter
- Accutracker DX Noninvasive Blood Pressure (NBP) Monitor
- DINAMAP® PRO Series Monitors
- Antenna System
- Receiver System
- Unity Network
- CIC Pro Clinical Information Center
- 4 Connection
- 5 Maintenance
- 6 Telemetry Setup
- 7 Admit/View a Patient
2-12 ApexPro Telemetry System Revision D
2001989-134
Safety: For Your Safety
Notes
Put the system in a location where you can easily see the screen and
access the operating controls.
This product is not likely to cause abnormal operation of other
patient-connected equipment such as cardiac pacemakers or other
electrical stimulators. Exceptions are noted in the pacemaker
monitoring section, if applicable.
This product is protected against the effects of cardiac defibrillator
discharges to ensure proper recovery, as required by test standards.
This equipment is suitable for connection to public mains as defined
in CISPR 11.
This equipment is suitable for use in the presence of electrosurgery.
Reference Literature
Medical Device Directive 93/42/EEC.
EN 60601-1/1990 + A1: 1993 + A2: 1995: Medical electrical equipment.
General requirements for safety.
EN 60601-1-1:2001: General requirements for safety. Safety
requirements for medical electrical systems.
IEC Publication 513/1994: Fundamental aspects of safety standards for
medical equipment.
ROY, O.Z.: Summary of cardiac fibrillation thresholds for 60-Hz currents
and voltages applied directly to the heart. Med. & Biol. Engn. &
Computing 18: 657...659 (1980).