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
Revision D ApexPro Telemetry System CE-7
2001989-134
CE Marking Information
General Information
This manual is an integral part of the product and describes its
intended use. It should always be kept close to the equipment.
Observance of the manual is a prerequisite for proper product
performance and correct operation and ensures patient and operator
safety.
The symbol means ATTENTION: Consult accompanying
documents.
Information which refers only to certain versions of the product is
accompanied by the model number(s) of the product(s) concerned.
The model number is given on the nameplate of the product.
The warranty does not cover damages resulting from the use of
accessories and consumables from other manufacturers.
GE Medical Systems Information Technologies is responsible for the
effects on safety, reliability, and performance of the product, only if:
assembly operations, extensions, readjustments, modifications,
or repairs are carried out by persons authorized by GE Medical
Systems Information Technologies;
the electrical installation of the relevant room complies with the
requirements of the appropriate regulations; and,
the device is used in accordance with the instructions for use.
All publications conform with the product specifications and
applicable IEC publications on safety and essential performance of
electromedical equipment as well as with applicable UL and CSA
requirements and AHA recommendations valid at the time of
printing.
The GE Medical Systems Information Technologies quality
management system complies with the international standards EN
ISO 9001 and EN 46001, and the Council Directive on Medical
Devices 93/42/EEC.