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-1
2001989-134
CE Marking Information
CE Marking Information
Compliance
The ApexPro telemetry system bears CE mark CE-0459 indicating
conformity with the provisions of the Council Directive 93/42/EEC
concerning medical devices, and fulfills the essential requirements of
Annex I of this directive. The product is radio-interference protection
class A in accordance with EN 55011.
The country of manufacture can be found on the equipment labeling.
The product complies with the requirements of standard EN 60601-1-2
“Electromagnetic Compatibility-Medical Electrical Equipment.”
The safety and effectiveness of this device has been verified against
previously distributed devices. Although all standards applicable to
presently marketed devices may not be appropriate for prior devices (i.e.
electromagnetic compatibility standards), this device will not impair the
safe and effective use of those previously distributed devices. See user's
information.