All rights reserved. Contents of this publication may not be reproduced in any form without
the written permission of Spacelabs Healthcare. Products of Spacelabs Healthcare are
covered by U.S. and foreign patents and/or pending patents. Printed in U.S.A. Specifications
and price change privileges are reserved.
Spacelabs Healthcare considers itself responsible for the effects on safety, reliability and
performance of the equipment only if:
• assembly operations, re-adjustments, modifications or repairs are carried out by persons
authorized by Spacelabs Healthcare, and
• the electrical installation of the relevant room complies with the requirements of the
standard in force, and
• the equipment is used in accordance with the operations manual.
Spacelabs Healthcare will make available, on request, such circuit diagrams, component part
lists, descriptions, calibration instructions or other information which will assist appropriately
qualified technical personnel to repair those parts of the equipment which are classified by
Spacelabs Healthcare as field repairable.
Spacelabs Healthcare is committed to providing comprehensive customer support beginning
with your initial inquiry through purchase, training, and service for the life of your Spacelabs
Healthcare equipment.
CORPORATE OFFICES
Corporate Headquarters
Spacelabs Healthcare
35301 SE Center Street
Snoqualmie, WA 98065
U.S.A.
Telephone: (1) 800-287-7108
Telephone: (1) 425-396-3300
Authorized EC Representative
Spacelabs Healthcare, Ltd.
43 Moray Place
Edinburgh, EH3 6BT
United Kingdom
Telephone: 44 (0) 131 240 6481
Fax: 44 (0) 131 240 6459
Please refer to http://www.spacelabshealthcare.com/en/company/trademarks for a full listing of
Spacelabs Healthcare trademarks. Other brands and product names used herein are trademarks of their
respective owners.
Caution:
US Federal law restricts the devices documented herein to sale by, or on the
order of, a physician.
Before use, carefully read the instructions, including all warnings and cautions.
The Ultraview® Digital Telemetry System is comprised of patientworn transmitters, a ceiling-mounted antenna system, receiver
modules, receiver module housings, central surveillance monitors,
and central strip recorders. Portable bedside patient monitors are
often incorporated into the telemetry system. A patient-worn
ambulatory blood pressure (ABP) monitor and its management
software may also integrate into the system.
Notes:
• Spacelabs Healthcare products and parts are designed and
manufactured in accordance with the Food and Drug
Administration’s (FDA) Quality System Regulation (QSR) and
in compliance with all applicable regulatory requirements. To
ensure proper operation in accordance with these guidelines,
Spacelabs products must be maintained by trained
technicians using only authorized replacement parts.
Spacelabs replacement parts have been thoroughly tested to
ensure reliable performance and include all of the latest
improvements and design changes available to ensure a
quality repair process.
• Prior to deployment of 90341/90343/90347/91341/91343/
91347 transmitters, hospital registration and deployment
registration must be performed with the WMTS Frequency
Coordinator. Refer to www.ashe.org for more information.
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1-1
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91341/91347 (ECG)
digital telemetry
transmitter
90341/90347
(ECG)
digital telemetry
transmitter
90343
(ECG and SpO
2
)
digital telemetry
transmitter
91343
(ECG and SpO2)
digital telemetry
transmitter
Diversity antenna
system
90478-Q receiver
module
90478-T/V
receiver module
SL2200/SL2400/SL2600
bedside or portable monitor
SL3800 central
monitor with SDLC
cabling (1)
90479-A/B/C Digital telemetry
receiver module housing
1
LTRAVIEW DIGITAL TELEMETRY -
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I NTRODUCTION
Figure 1-1 Ultraview Digital Telemetry system components
The patient-worn transmitter is a small, battery-powered device that
collects physiologic data and communicates it via radio frequencies
(RF) through a system of ceiling-mounted antennas to a receiver
and central monitoring station for viewing and analysis. The
transmitter must be in range of a receiver module or its ceilingmounted antenna system for surveillance monitors to display
waveforms and generate alarm events and patient data (trends).
Spacelabs offers several patient-worn transmitter models that vary
in frequency-operation and clinical functionality, described in Table
1-1 and in Table 1-2 on page 1-7.
I NTRODUCTION
1-4
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U LTRAVIEW DIGITAL TELEMETRY
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Table 1-1 Patient-Worn Transmitter Specifications: 90341, 90347, and 90343
I NTRODUCTION
Model,
frequency
(MHz), &
country
Regulatory
approvals
ECG onlyECG only
90341-74: 174.0125 to
197.9875 MHz (US)
90341-16: 198.0125 to
216.9875 MHz (US)
90341-16-IEC: 202.6875
to 205.1375 MHz
(Netherlands)
90341-50: 458.525 to
458.0875 MHz (UK)
90341-32: 433.0625 to
434.7875 MHz (Germany,
Austria, Czech Republic,
France, Italy, Spain,
Portugal, Belgium,
Netherlands, Australia)
90341-34: 433.075 to
433.350 MHz (Spain)
90341-52: 468.625 to
468.675 MHz (Finland)
90341-42: 438.025 to
439.975 MHz (Sweden)
90341-46: 440 to
441.975 MHz (Norway)
90341-40: 469.1625 to
469.850 MHz (Australia)
90341-53: 470 to
470.500 MHz (New
Zealand)
90341: 460 to 470 MHz
(US, Canada)
90341-05: 608 to
614 MHz
IncompatibilityNot compatible with 9034X telemetry processors
Output power<5 mW EIRP, max
Multiparameter
(ECG & SpO
A patient-activated RECORD button can be used to initiate an event
recording at the system printer (this feature must first be enabled at
the monitor using the ECG TM SETUP menu). All four telemetry
patient-worn transmitters incorporate a low battery indicator that
flashes when the battery capacity has approximately three hours of
remaining energy.
• Wideband (50 kHz) 90343, 90347, 91343, and 91347 ECG
transmission enables you to view two of seven available leads
(from four vectors with a synchronized RF digital signal).
• Narrowband (25 kHz) 90341/91341 ECG transmission enables
you to view either two of two or two of four available leads
(from two vectors with a synchronized RF digital signal).
• The 91341, 91343, and 91347 transmitter provides functionality
for local lead fault indicators and user-configurable transmit
frequency operation.
The front labels on the transmitters are color coded to their
compatible receivers.
• The 90341, 90343, and 90347 transmitter labels are blue.
• The 91341, 91343, and 91347 transmitter labels are green.
)
2
Selecting Options for the 90341/91341/91347 Lead Display
There are two operational modes available with the 90341 dual-lead
transmitter: (1) the standard mode which offers a choice of one V
lead (V1-6), plus lead II, or (2) the limb lead mode which offers
choices of the leads I, II, III, AVR, AVL, or AVF. The standard mode is
available if the chest lead is applied. The limb lead mode is available
when there is not a chest lead applied. Loss of the chest electrode
changes the ECG - LEAD SELECT menu to the limb lead mode if the
left arm, left leg, and right arm electrodes are intact.
Note:
Both modes work correctly with or without the right leg
electrode attached. However, for optimum performance, the
right leg electrode should always be used.
1-8
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U LTRAVIEW DIGITAL TELEMETRY
Lead fault indicators
(91341 and 91347)
ERVICE MANUAL
- S
I NTRODUCTION
Table 1-3 90341/91341 Lead Options
Connected Electrodes (X)
C
(C)
LA
(L)
XXXXV1-6 and II (standard mode)
XXXIII (standard mode)
XXXI (standard mode)
XXTotal lead failure (standard mode)
XXXII (standard mode)
XXNone (lead failure)
XXNone (lead failure)
XNone (lead failure)
LL
(F)
RA
(R)
XNone (lead failure)
Val id Le ad Vecto rs
XNone (lead failure)
XNone (lead failure)
None (lead failure)
XXIII (limb lead mode)
XXI (limb lead mode)
XXII (limb lead mode)
XXXI, II, III, AVR, AVL, AVF (limb lead mode)
Notes:
• If one of the leads fails, a lead fault message will display in the
upper-left corner of the waveform zone. If there is not a valid
lead vector, the message LEADS OFF displays and an alarm
tone sounds.
• The 91341 and 91347 dual-lead transmitters have blue
indicators near the ECG connector block. Each indicator
provides the status of its respective lead wire and flashes if its
lead wire is disconnected from the skin electrode or if the skin
electrode makes poor electrical contact with the patient.
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Figure 1-2 91341/91347 transmitter
1-9
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Multiparameter Transmission (90343/91343)
The following data can be transmitted by the multiparameter,
patient-worn transmitter:
•SpO
• NIBP (with the model 90217 ABP monitor)
Battery Compartment SIP switches
(with Nellcor pulse oximetry sensors)
2
-saturation
-SpO
sensor status
2
-pulse rate
-systolic
-diastolic
-mean pressure
-measurement time
-alarm conditions
I NTRODUCTION
SpO2 data averaging is used to smooth the oximetry saturation
value by averaging the patient input values over 4, 8, or 16 seconds.
This selection is made by setting the SIP switches 1 and 2 beneath
the battery compartment in the multiparameter, patient-worn
transmitter. The default value is 8 seconds. Refer to Figure 1-3 on
page 1-11.
Caution:
Avoid using pencils or sharp instruments to configure the SIP
switches.
Notes:
• Setting both SIP switches 1 and 2 to ON disables SpO
transmission.
•To enable SpO
and re-install the battery.
• Disabling SpO
transmitter lengthens battery life.
SIP switch 1SIP switch 2Effect
OFFOFF4 seconds averaging enabled
, remove the battery, set the selected interval,
2
operation in the 90343/91343 patient-worn
2
Table 1-4 SIP switch 1 and 2 Settings
data
2
1-10
OFFON8 seconds averaging enabled (default)
ONOFF16 seconds averaging enabled
ONONDisable SpO
operation
2
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U LTRAVIEW DIGITAL TELEMETRY
1 2 3 4
SpO
2
averaging
period
SpO
2
reading
interval
5 6 7 8
ON
OFF
enable
normal
enabledisable
IABP
disable
NIBP
Adult
enable
NIBP
enable
IABP
enable
Neonate
enable
Service use
operation
ERVICE MANUAL
- S
I NTRODUCTION
The current setting of the SpO2 averaging period can be displayed
by pressing the ECG CHANNEL FORMAT key and enabling SpO
Figure 1-3 SIP switch setting in battery compartment
The sampling interval selection enables you to determine how often
an SpO
measurement will be taken. Less frequent SpO2 readings
2
can extend the usable life of the battery. (Refer toTransmitter
Battery Service Life1(hours) on page 1-12 for more information.) This
selection is made by setting SIP switches 3 and 4 beneath the
battery compartment. The default setting is CONTINUOUS.
Caution:
No SpO2 monitoring occurs between episodic sampling intervals.
Clinical practice or medical judgement should be used in selecting
continuous or episodic SpO
patient.
Table 1-5 SIP switch 3 and 4 Settings
monitoring mode for each specific
2
.
2
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SIP switch 3SIP switch 4Effect
Caution:
SIP switch 8 must remain OFF for normal operation.
OFFOFFContinuous sampling (default)
OFFON2-minute sampling interval
ONOFF5-minute sampling interval
ONON30-minute sampling interval
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Additional Data Transmitted
The following information is also transmitted:
• Patient record
• Low battery indicator
•Pacer flag
• Transmitter type and channel number codes
•Electrode connection status
Transmitter Batteries
The patient-worn transmitters use a 9V lithium or alkaline battery. A
yellow LED flashes when battery level is low.
Table 1-6 Transmitter Battery Service Life1(hours)
I NTRODUCTION
Battery
Type
Load
Conditions
90343,
91343
90341,
90347,
91341,
91347
9 Volt Alkaline (ANSI/NEDA 1604A)9 Volt Lithium (ANSI/NEDA 1604LC)
ECG
2
Only
ECG and
Continuous
SpO
2
ECG and 2minute
Episodic
SpO
2
ECG and 5minute
Episodic
SpO2
482436384012060100104106
5 2N /AN /AN /AN /A1 32N /AN /AN /AN /A
1 Operational service life (in hours) assuming a new alkaline battery
(minimum 580 mAH capacity) or lithium battery (minimum 1200
mAH capacity) used until the local low battery indicator begins to
flash.
2
NIBP operations from a 90217 ABP monitor sending readings to
the 90343/91343 multiparameter telemetry transmitter. The
90217 ABP monitor will inflate a standard size adult cuff at least
240 times with alkaline batteries.
ECG and
30-minute
Episodic
SpO2 and
NIBP
ECG
Only
ECG and
Continuous
SpO
2
ECG and 2minute
Episodic
SpO2
ECG and
5-minute
Episodic
SpO
2
ECG and
30-minute
Episodic
SpO
2
1-12
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I NTRODUCTION
Warning:
Medical telemetry spectrum allocations may be assigned to
frequencies already allotted to other priority users. This means
that telemetry operations may be exposed to radio frequency
interference that may disrupt or impede telemetry patient
monitoring. Customers are urged to regularly consult with
applicable local and federal regulatory agencies (e.g., FCC, FDA,
etc.) regarding the locations and frequencies of other spectrum
users in the customer’s geographic area. Spacelabs Healthcare
Service Representatives may be able to assist you in reconfiguring
your equipment frequencies to reduce this risk of potential
interference. Spacelabs cannot, and does not, guarantee
interference-free telemetry operation.
Cautions:
• This device has a limited bandwidth from .05 to 30 Hz, which
may adversely affect the recording of high frequency
components in the ECG signal, especially when the morphology
of the ECG changes rapidly.
• This device has a limited dynamic range of ±4 mV, which may
render the device vulnerable to saturation by ECG signals with
amplitudes higher than 4 mV.
• Use only the following solutions per the manufacturer’s labeling:
Isopropyl Alcohol (70%), Hydrogen Peroxide, Cidex, Betadine,
and chlorine bleach. Use of cleaning solutions other than those
listed will VOID the warranty on the equipment cases.
• Refer to Cleaning/Disinfecting on page 4-2 for additional
instructions.
Receiver Module (90478)
The 90478 telemetry receiver module analyzes the waveform sent
by a patient-worn transmitter. This analysis consists of evaluating
dual-lead arrhythmias and ST segments. The receivers also retain
patient data such as alarm events, arrhythmia and ST-segment
trends. On the central monitor’s display, each ECG waveform zone
generally represents the user interface for one receiver module.
Receiver modules are generally inserted into a 90479-A/B/C
receiver housing. The receiver housing allows each receiver module
to be directly connected to the antenna system via input connectors
(BNC) labelled ANT 1 and ANT 2. The receiver housing is connected
to a central monitor by an SDLC cable.
The 90478-Q receiver module can also reside in a bedside monitor.
Small whip antennas attach directly to the receiver’s input
connectors. In this case, the patient-worn transmitter may wirelessly
communicate directly with the receiver module and is not required
to connect to the ceiling-mounted antenna system.
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I NTRODUCTION
Each receiver module operates within a specific frequency band. A
receiver module can be tuned to any patient-worn transmitter’s
channel (operating frequency), provided the channel falls within the
same frequency band.
Monitor options provide 24 hours of trended data that can be
displayed in 2-, 6-, 12-, and 24-hour segments. Data is stored in 1minute resolution.
The receiver module counts as 1 or 2 parameters when computing
parameter capacity for monitors:
• 1 displayed ECG lead = 1 parameter
• 2 displayed ECG leads = 2 parameters
Signal reception requires the use of a different frequency (channel)
assigned to each receiver. In the U.S.A., these transmission
frequencies are regulated by the Federal Communications
Commission (FCC). In other countries, these transmissions are
regulated by the local communications authority.
Telemetry use is managed through the operation of the Ultraview
Care Network Module Configuration Manager. Refer to the Module Configuration Manager System Administration Guide (P/N 0701245-xx), located on CD-ROM P/N 084-1101-xx.
The high level analog output has the following characteristics:
ECG 1Used for defibrillator synchronization
Connector:3-conductor TT phone jack
Dynamic Range±5 mV, ±10% (rti)
GainECG × 1000, ±5%
Bandwidth0.05 to 30 Hz, ±10% (-3 dB)
Table 1-7 Transmitter/Receiver Compatibility
Transmitter
Model
90341-05
90343-05
90347-05
90343-16202.65 - 205.1590478-N, 90478-O
91347
91341
91343
91347
91341
1
91343
1
The 91341/91343/91347 ECG telemetry is used in conjunction with
the Multi-Band Active Antenna system to down-convert 1400
MHz emissions into the 600 MHz band for detection.
Operating Frequency
Range (MHz)
608 - 61490478-Q
1395 - 140090478-T
1427 - 1431.590478-V
Compatible
Receiver Module
1-14
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U LTRAVIEW DIGITAL TELEMETRY
TIP — Analog ECG out
RING — defib sync. input
sleeve — ground
1
2
3
4
5
1
high level output (hlo)
2
LED
3
ANT 1
4
ANT 2
5
handle
ERVICE MANUAL
- S
I NTRODUCTION
Table 1-8 Monitor Software Compatibility
Monitor
PC Express®Yes3.6 7.0 5
PC Scout
UCW
Ultraview 1030/1050Yes1.02.01
Ultraview 1500Yes1.03.03
Ultraview 1600Yes1.03.03
Ultraview 1700Yes1.06.61
Ultraview SL2400Yes2.00.03
Ultraview SL2700/2800/3800Yes2.00.03
®, PC Ranger®Yes3.53.36
®Yes1.0 6. 61
Compatible with
Ultraview Telemetry?
Minimum Software Version
Needed for Compatibility
Receiver Electrical Requirements
Power Consumption≤ 5.0 watts
External IndicatorsLED lights when user accesses control
Receiver Physical Dimensions
Height11.33 cm (4.46 inches)
Width5.69 cm (2.24 inches)
Depth17.78 cm (7 inches)
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Weight1.09 kg (2.4 pounds)
Figure 1-4 Receiver module
1-15
U
1
2
3
4
1 receiver
module slot
(for eight
modules)
2 antenna cable
(pulled out)
3 antenna cable
(stowed)
LTRAVIEW DIGITAL TELEMETRY -
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I NTRODUCTION
Warnings:
• Telemetry systems may be more susceptible to interference than hardwired systems,
which may impact patient safety.
• Operation of hand-held, wireless telephone equipment (cordless telephones, cellular
telephones) near telemetry systems may cause interference and should be
discouraged. While personal communication devices are powered ON, a separation
of >6.5 feet (>2 meters) should be maintained between personal communication
devices and interior walls, the patient cables, and any electronic medical device to
which the patient may be connected. Patients should not use any type of electronic
communication equipment while connected to any electronic medical device without
an on-site evaluation by the biomedical staff. Two-way radio equipment and other
personal communication devices must be evaluated on site to determine if
additional space limitations are needed.
• Do not install a telemetry receiver module into a bedside which is currently equipped
with any other ECG module, hardwired or telemetry (or SpO
module if the 90343 or 91343 is operating with that specific receiver module). Doing
so may result in inaccurate patient data displays at remote monitors.
• Only 90478-Q modules may be installed in transport monitors.
module or NIBP
2
Receiver Housing (90479-A/B/C)
The receiver housing is used for centralized telemetry applications
and connects directly to a central monitor through an SDLC cable. It
provides up to eight plug-in slots for telemetry receiver modules.
Additional receiver modules may be utilized by connecting another
receiver housing to the SDLC bus (refer to SDLC Configurations on
page 2-6). A diversity antenna system connects to the back of the
housing. Special dual cable assemblies on the front panel plug into
each receiver’s antenna inputs (ANT 1 and ANT 2). Except for power
ON/OFF switches (AC mains and battery), there are no operator
controls. An indicator lamp on the front panel lights when the unit is
connected to AC power. An internal battery provides at least ten
minutes of operation when AC power is lost. (Refer to Receiver
Housing Power Operation on page 2-11.)
1-16
Figure 1-5 90479-A receiver housing front view
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U LTRAVIEW DIGITAL TELEMETRY
1
2
3
1 receiver
module slot
(for eight
modules)
2 antenna cable
(stowed)
3 AC line status
light
ERVICE MANUAL
- S
Figure 1-6 90479-B/C receiver housing front view
Receiver Housing Physical Dimensions
Height30.5 cm (12.0 inches)
I NTRODUCTION
Width34.3 cm (13.5 inches)
Depth44.5 cm (17.5 inches), includes protective cover
Weight14.6 kg (32 pounds), without modules loaded
23.6 kg (52 pounds), with eight modules loaded
Receiver Housing Power Requirements
100 to 120 VAC, 50/60 Hz, 2 A
220 to 240 VAC, 50/60 Hz, 1 A
Receiver Housing Environmental Requirements
Operating
Temperature10° to 40° C (50° to 104° F)
Humidity95% (non-condensing)
Altitude0 m to 3048 m (0 to 10,000 feet)
BTU Out256 BTU/h with eight modules loaded
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Cooling50 CFU
1-17
U
1
2
3
7
6
4
5
1
23
6
5
7
4
90479-B/C
90479-A
LTRAVIEW DIGITAL TELEMETRY -
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S
Storage
Temperature-40° to 65° C (-40° to 149° F)
Humidity95% (non-condensing)
Altitude-152.4 m to 12,192 m (-500 to 40,000
Receiver Housing Rear Panel
I NTRODUCTION
feet)
1-18
Figure 1-7 Receiver housing rear panel
1 SDLC cable
2 SDLC connectors (4)
3 High level outputs
4 AC power switch and fuse assembly
5 Inputs for diversity antennas (ANT 1, ANT 2)
6 SDLC terminator
7 DC power ON/OFF switch
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U LTRAVIEW DIGITAL TELEMETRY - SERVICE MANUAL
Setup
Unpacking
Each patient-worn transmitter, receiver module, and receiver
housing are packaged individually. Unpack the transmitter and its
accessories, the SpO
Unpacking the Patient-Worn Transmitter on page 2-2). Carefully
unpack the receiver housing (refer to Unpacking the Receiver
Housing on page 2-3). When removing the packing material around
the front panel take care not to damage the antenna cables. These
cables should be properly stowed in the appropriate cable ports on
the front bezel [refer to Receiver Housing (90479-A/B/C) on
page 1-16].
Ensure that you do not turn the rear panel DC power switch ON. This
unnecessarily drains the battery. Remove the accessories from the
packing carton (e.g., power cord, power cord retainer, SDLC cable,
and manual) to inspect each for damage. Also inspect the air filter
on the bottom of the receiver housing.
Unpack each receiver module from its shipping container for
inspection (refer to Unpacking the Receiver on page 2-3). Save all
packing materials in case a part must be returned.
adapter cable, and its accessory kit (refer to
2
Caution:
Open containers carefully to prevent any damage to equipment.
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Note:
If your equipment shows evidence of shipping damage,
immediately notify the carrier and Spacelabs Healthcare.
2-1
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Unpacking the Patient-Worn Transmitter
To unpack the transmitter
Notes:
• For the 90341 illustration, refer to Drawing 1, Sheet 3 of 3,
right side.
• For the 90343/91343 illustration, refer to Drawing 2, Sheet 3
of 3, right side.
• For the 90347 illustration, refer to Drawing 5, Sheet 3 of 3,
right side.
• For the 91341/91347 illustration, refer to Drawing 6, Sheet 1 of
2, right side.
1 Cut the white label using a knife (with the transmitter’s serial
number) that holds the container flap shut, along the edge of
the container.
2 Pull the container flap open. Pull from the edge cut-outs of the
cardboard insert to expose the transmitter.
3 Pull the transmitter out of the container, by holding the
transmitter from opposite ends at the cut-outs in the
cardboard insert.
4 Remove transmitter from its bag. The 90343/91343 transmitter
includes two connector caps.
5 Remove the cardboard insert from the container to expose the
SpO
adapter cable assembly (90343/91343 only), the
2
connector cap kit (90343/91343 only) and the transmitter
accessory kit.
6 Open the accessories bag (except for the connector cap kit
which includes four spare caps), to verify its contents: SpO
adapter cable, ECG lead wire set (5 lead wires), transmitter
pouch, two 9-volt batteries, belt clip, and related screws.
7 Retain the Wireless Medical Telemetry Service (WMTS)
registration card.
8 Save all packing materials in case the transmitter must be
returned.
S ETUP
2
2-2
Notes:
• Prior to deployment of 90341/90343/90347/91341/91347/
91343 transmitters, hospital registration and deployment
registration must be performed with the WMTS Frequency
Coordinator.
• Refer to www.ashe.org for more information.
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ERVICE MANUAL
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Unpacking the Receiver Housing
To unpack the receiver housing (refer to the
Drawing 12, Sheet 1 of 1)
1 Cut the tape that holds the container flaps shut using a knife at
the container top end.
The container top end is up when the writing on the sides of the
box reads right-side-up.
2 Remove the two bagged accessories situated on the top foam
insert and set them aside.
3 Carefully turn the container upside down with all four flaps out
of the way.
4 Gently pull the container up and out of the way, to expose its
contents.
5 Remove the top foam insert exposing the receiver housing
bottom end.
6 Set aside the third bagged accessory containing the AC power
cord.
7 Turn the receiver housing right side up, on its feet.
8 Remove the foam insert at the top of the receiver housing and
the front panel foam rails protecting the protruding antenna
cables. Cables must remain properly stowed in the appropriate
front panel cable ports.
9 En sure t hat you do not turn t he r ea r pa nel DC pow er swi tch ON .
This is unnecessary and drains the battery.
10 Open the three bagged accessories and verify that the
contents include the power cord, the power cord retainer and
bracket, the related screws and washer, the SDLC terminator,
the cable adapter assembly (DB26HD male to DB9 male), and
the documentation.
11 Inspect the air filter on the bottom of the receiver housing.
12 Save all packing materials in case the receiver housing must be
returned.
S ETUP
Unpacking the Receiver
To unpack the receiver (refer to Drawing 3,
Sheet 2 of 2)
1 Cut the white label using a knife (with the receiver’s serial
2 Pull the container flap open.
3 Remove the receiver from the container.
4 Save all packing material in case the receiver must be returned.
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number) that holds the flap shut, along the edge of the
container.
2-3
U
SDLC terminator
free SDLC port
LTRAVIEW DIGITAL TELEMETRY -
ERVICE MANUAL
S
Receiver Housing Configuration
To ready the 90479-A/B/C receiver housing
for operation
1 Set the receiver housing in the area where it will be operated.
Choose a location that provides good ventilation, and ensure
that air flow for the air intake (bottom) and exhaust (rear top)
are not obstructed.
2 Verify that the receiver housing is configured for the correct AC
line voltage by inspecting the line voltage indicator on the rear
panel power entry module. The correct setting for input
voltages from 100 to 120 VAC is 115. The correct setting for
input voltages from 220 to 240 VAC is 230. If the line voltage
setting is incorrect, refer to AC Mains Voltage Selection on
page 2-8.
3 Attach the AC power cord and install the power cord retainer
(follow the instructions).
4 Cable the SDLC connections (for illustrations of other SDLC
connections, refer to SDLC Configurations on page 2-6).
aTo configure SDLC connections for a typical eight-receiver
housing, connect one end of the SDLC cable to the free SDLC
port on the rear of the unit. Ensure that the SDLC terminator
is in place.
S ETUP
Note:
An SDLC cable is not provided with the receiver housing. To
connect to the central monitor, contact Spacelabs Healthcare
customer service for instructions.
Figure 2-1 Rear panel
bWhen finished routing the SDLC cables, position the receiver
housing in its permanent location.
5 Connect the free end of the 9-pin SDLC cable to the SDLC port
on the central monitor or module housing.
6 Connect the diversity antenna down leads to the two antenna
ports on the rear panel.
2-4
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