Philips makes no warranty of any kind with regard to this material, including, but
not limited to, the implied warranties of merchantability and fitness for a particular
purpose. Philips shall not be liable for errors contained herein or for incidental or
consequential damages in connection with the furnishing, performance or use of
this material.
This document contains proprietary information that is protected by copyright. All
rights are reserved. No part of this document may be photocopied, reproduced or
translated to another language without prior written consent of Philips Medical
Systems. The information contained in this document is subject to change without
notice. Philips assumes no responsibility for the use or reliability of its software on
equipment that is not furnished by Philips.
United States federal law restricts these devices to sale by or on the order of a
physician.
2
Intended Use
DescriptionThe Philips M1032A VueLink module is a plug-in module for use with a Philips
IntelliVue, V24 or V26 Patient Monitor or a Philips CMS Patient Monitoring
System.
The Philips M1032A VueLink module is powered via the patient monitor.
PurposeThe Philips M1032A VueLink module transmits information from a connected
external device to a Philips IntelliVue, V24 or V26 Patient Monitor or a Philips CMS
Patient Monitoring System. The Philips M1032A VueLink module is not a
therapeutic device.
Environ-
ment
The Philips M1032A VueLink module is intended to be used in a clinical
environment by trained healthcare professionals. It is not intended for home use.
3
Indications for Use
ConditionThe use of a Philips M1032A VueLink module is generally indicated when the
clinician decides there is a need to include the physiological and device parameters
and waves and alarms generated by external devices into the Philips IntelliVue, V24
or V26 Patient Monitor or a Philips CMS Patient Monitoring System.
Part of Body
or Type of
Tissue with
Which the
Device Inter-
acts
Frequency
of Use
Physiologi-
cal Purpose
Patient Pop-
ulation
Prescrip-
tion Versus
Over-the-
Counter
The Philips M1032A VueLink module does not contact the body or tissue of the
patient. Signals are obtained from external devices.
The Philips M1032A VueLink module is indicated for use when prescribed by a
clinician.
The Philips M1032A VueLink module is indicated when the purpose is to gain
information for treatment, to assess adequacy of treatment, or to rule out causes
of symptoms. The Philips M1032A VueLink module is well suited for patient
monitoring.
Please refer to the documentation describing the external device.
The Philips M1032A VueLink module is a prescription device.
4
Warnings, Cautions and Notes
In this guide:
Warning
•A
warning
alerts you to a potential serious outcome, adverse event or
safety hazard.
Failure to observe a warning may result in death or serious injury to the
user or patient.
CautionA caution alerts you where special care is necessary for the safe and effective
use of the product.
Failure to observe a caution may result in minor or moderate personal injury
or damage to the product or other property, and possibly in a remote risk of
more serious injury.
NoteA note gives special instructions to highlight an operating procedure or practice.
Notes may precede or follow the applicable text.
5
Responsibility of the Manufacturer
Philips Medical Systems only considers itself responsible for any effects on safety,
reliability and performance of the equipment if:
•assembly operations, extensions, re-adjustments, modifications or repairs are
carried out by persons authorized by Philips, and
•the electrical installation of the relevant room complies with national
standards, and
•the Philips M1032A VueLink module is used in accordance with the
instructions for use contained in this document, and in the relevant chapter
of the user documentation for the patient monitor into which the module is
plugged (Philips IntelliVue, V24 or V26 Patient Monitor or a Philips CMS
Patient Monitoring System).
Warning
•Failure on the part of the responsible individual hospital or institution
employing the this equipment to implement a satisfactory maintenance
schedule may cause undue equipment failure and possible health
hazards.
The maintenance schedule is defined in the Testing and Maintenance
chapter of the IntelliVue Patient Monitor Service Guide, the Philips CMS
Patient Monitoring System Service Guide, or the Philips V24/V26
Component Monitoring System Service Guide, corresponding to your
monitor.
NoteNot all the device drivers are available in all countries.
The Instructions for Use for all drivers are translated into the following languages:
Czech, Danish, Dutch, Estonian, Finnish, French, German, Greek, Hungarian,
Italian, Japanese, Norwegian, Polish, Portuguese, Romanian, Russian, Simplified
Chinese (China), Slovak, Spanish, Swedish, Traditional Chinese (Taiwan), Turkish.
The driver software may not be available in all of these languages. Please refer to the
CMS-PM softserver (
subfolder Vuelink, subfolder Additional Information) for a list of the translated
drivers
that are available.
Please also check your local regulatory and business requirements for permission to
sell.
Philips authorized technical personnel are responsible for the setup, configuration
and repair of the VueLink module and all related Philips equipment. The
configuration, setup and repair of external devices furnished by manufacturers other
than Philips Medical Systems must be carried out by local site personnel, or by
representatives of the external device manufacturer.
Philips Medical Systems is not responsible for any problems arising from inaccurate
or erroneous data displayed on the Philips patient monitor that is received from
external devices furnished by manufacturers other than Philips Medical Systems.
Philips Medical Systems makes every effort to ensure that signal names are
maintained between the Philips patient monitor and any interfaced external devices.
However, signal names within the Philips patient monitor also need to remain
consistent. This means that in some cases the wave and numeric labels used on the
Philips monitor may be different from those used on the interfaced external device.
Philips Medical Systems will not be held responsible for any errors in the
configuration of the VueLink module for connection to free-analog devices.
If manufacturers other than Philips Medical Systems make changes to any VueLink
supported device, Philips Medical Systems will try to ensure that interfacing to that
device remains possible. However, Philips Medical Systems reserves the right to
discontinue interfacing to any device.
7
Introduction
This Service Guide contains technical details for the connection of external devices
to the VueLink module. It is not a comprehensive, in-depth explanation of the
product architecture or technical implementation.
Who Should
Use This
Guide
How to Use
This Booklet
This guide is for biomedical engineers or technicians responsible for connecting
external devices to Philips patient monitoring systems using the VueLink module.
This booklet provides information on the worldwide external devices that can be
connected to the VueLink module. It should be printed and inserted into Appendix
A of the VueLink Module Handbook, completely replacing the existing worldwide
driver information.
The information contained in this document is subject to change without notice.
There are two different ways to connect your Device to VueLink:
•Connection via a Supported Device driver.
This uses one of the following device outputs:
–Analog
– RS-232 Digital
– Analog/Digital combination
•Connection via a Free Analog Device driver.
This only uses device analog outputs.
Supported Device Drivers
Supported Device Drivers are preconfigured in the VueLink module. A dedicated
ready-prepared VueLink cable is available for connecting the external device to the
module. (Please refer to page A-4 for cable part numbers).
Connecting your Device to VueLink
Free Analog Device Drivers
Free Analog Device Drivers must be manually configured into the module at
installation. A Free Analog VueLink cable is available for connecting the Free
Analog external device to the VueLink module. One end of the cable is
unterminated and must be prepared for connection to the external device on-site.
(Please refer to page B-4 for cable option part numbers).
This appendix contains information about the supported devices that can be
connected to the VueLink module. The following information is provided for each
supported device:
•The part number of the corresponding device driver.
•The configuration settings required on the external device.
•The placement of the output connectors on the external device.
A cable matrix has also been compiled, detailing the cable part numbers for each
supported device.
CautionOnly use cables specified by Philips Medical Systems when connecting
supported devices to the VueLink module. Use of unauthorized or incorrect
cables may result in damage to supported devices and may cause incorrect
data to be displayed on the Philips patient monitor.
The configuration settings required on the external devices are detailed on the
following pages. Procedures on how to configure the external devices are not
provided. Configuration procedures can be found in the documentation supplied
with the external devices. Philips personnel are only responsible for configuring
Philips manufactured external devices.
NoteThe signal labels used on the Philips patient monitor may be different from those
given on the external device. The labels used on the Philips patient monitor are
listed in the Philips M1032A VueLink External Device Instructions for Use.
Supported Device Information15
Driver Part Numbers for Supported Devices
Driver Part Numbers for Supported Devices
Each driver is allocated a part number, using the driver key detailed below:
16Supported Device Information
VueLink Cable Overview
3 Separate part numbers are assigned to each VueLink Cable:
M1032A KXX optionTo order a cable with a new module.
M1182A KXX optionTo order a cable for an existing module or for
M1032-XXXXX optionTo order a cable for an existing module from
The Supported Device cable options are detailed in the matrix opposite:
1. Old cable only available for support in case an existing cable fails.
2. NAD = North American Dräger
Supported Device Information21
VueLink Cable Overview
22Supported Device Information
Auxiliary Devices
Abbott Oximetrix 3 - SO2 Monitor
Device Driver Name: Abbott Oximetrix 3
Device Driver P/N:M1032-A07rl
Supported Devices:Oximetrix (R)3 SO
Connection:RS-232 Digital (Fixed configuration)
Switch Settings:Factory default
where:
r = revision
l = language
Monitor (version 104 and
2
105)
Baud Rate:1200
Word Length:8 bits
Stop Bits:1
Start Bits:1
Parity:None
A2
Auxiliary Devices23
Abbott Oximetrix 3 - SO2 Monitor
Abbott Oximetrix 3 - SO2 Monitor Rear Panel
Note
Please refer to the Philips M1032A VueLink External Device Instructions for Use
for exact details of waves, numerics, INOPs and alarms available from the external
device and via Philips
Please refer to the Philips M1032A VueLink External Device Instructions for Use
for exact details of waves, numerics, INOPs and alarms available from the external
device and via Philips
Please refer to the Philips M1032A VueLink External Device Instructions for Use
for exact details of waves, numerics, INOPs and alarms available from the external
device and via Philips
30Auxiliary Devices
patient monitoring network.
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