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-5
2001989-134
CE Marking Information
Radio and Telecommunication Terminal Equipment Directive
The ApexPro telemetry system transmitters bear the CE mark CE 0123
indicating conformity with the provisions of the Council Directive 1999/5/
EC of 9 March 1999 concerning R&TTE as tested by MKES BABT
Services GmbH Notified Body TUV (0123).
The product complies with the requirements of standard EN 300 220-1
[ETSI 300 220-1 v1.3.1]: “Electromagnetic Compatibility and Radio
Spectrum Matters (ERM); Short Range Devices (SRD); Part 1: Technical
Characteristics and Test Methods”.
Accutracker DX NBP Monitor
36.202.1 Immunity: ESD Air — Discharges in excess of ±6 Kv may
cause the cuff to deflate and the unit to lock
up. By turning the power switch off, then back
on (manual reset), the unit will be restored to
the user-defined settings and normal
operation.
The Accutracker DX blood pressure monitor
should be kept in the carrying pouch
supplied with each unit.
Care should be taken to minimize the ESD
potential when the Accutracker DX blood
pressure monitor is removed from the
pouch. This includes:
Handling the unit in an ESD-protected
area.
Maintaining humidity levels of 50%
relative humidity or greater.
Discharging ESD potentials on human
hands prior to handling the unit out of the
pouch.
CE Exception Table
EN60601-1-2 Clause 36 Exception Electromagnetic Environment Guidance