Mortara Instrument X12+ User manual

P/N 9515-164-50-ENG
X12+
User
Manual
__________________________________________________________________________________________
CAUTION: Federal law restricts this device for sale to and use by or on the order of a physician.

®
Copyright © 2004
by Mortara Instrument, Inc.
7865 N. 86th Street
Milwaukee, Wisconsin 53224
This document contains confidential information that belongs to Mortara Instrument, Inc. No part of this document
may be transmitted, reproduced, used, or disclosed outside of the receiving organization without the express written
consent of Mortara Instrument, Inc. Mortara is a registered trademark of Mortara Instrument, Inc. Ambulatory
X12+ is a trademark of Mortara Instrument, Inc.
REF NEW

i
Technical Support and Service
Headquarters
Mortara Instrument, Inc.
7865 North 86th Street
Milwaukee, WI 53224
Tel: [phone]
Tel: [phone]
Fax: [phone]
Internet: http://www.mortara.com
Europe Economic
Community Representative
Mortara Rangoni Europe, Srl
(European Headquarters, Italy)
Via Oradour 7
40016 S. Giorgio di Piano, BO
Tel: [phone]
Fax: [phone]
Service/Technical
Support Group
Mortara Instrument, Inc.
7865 North 86th Street
Milwaukee, WI 53224
Tel: [phone]
Service: 888.MORTARA
(888.667.8272)
Fax: [phone]
E-mail: [email protected]
24 Hour Technical Support
Same Day Shipment of Replacement Parts
Biomedical Training Classes
Extended Warranties/Service Contracts
Sales Support/
Supplies & Accessories
Mortara Instrument, Inc.
7865 North 86th Street
Milwaukee, WI 53224
Tel: [phone]
Fax: [phone]
E-mail: [email protected]
Mortara Instrument GmbH
(Germany)
Kaninenberghöhe 50
45136 Essen
Tel: [phone]
Fax: [phone]
Mortara Instrument B.V.
(The Netherlands)
H. Dunantplein 6
3731 CL De Bilt
Postbus 131
3720 AC Bilthoven
Tel: [phone]
Fax: [phone]

ii
Notices
Manufacturer’s Responsibility
Mortara Instrument, Inc., is responsible for the effects on safety and performance only if:
•Assembly operations, extensions, readjustments, modifications or repairs are carried out only by persons
authorized by Mortara Instrument, Inc.
•The device (Ambulatory X12+) is used in accordance with the instructions for use.
Responsibility of the Customer
The user of this product is responsible for ensuring the implementation of a satisfactory maintenance schedule.
Failure to do so may cause undue failure and possible health hazards.
Equipment Identification
Mortara Instrument, Inc. equipment is identified by a serial and reference number on the back of the device. Care
should be taken so that these numbers are not defaced.
Copyright and Trademark Notices
This document contains 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
Mortara Instrument, Inc.
Other Important Information
The information in this document is subject to change without notice.
Mortara Instrument, Inc. makes no warranty of any kind with regard to this material including, but not limited to,
implied warranties of merchantability and fitness for a particular purpose. Mortara Instrument, Inc. assumes no
responsibility for any errors or omissions that may appear in this document. Mortara Instrument Inc. makes no
commitment to update or to keep current the information contained in this document.

iii
Warranty Information
Your Mortara Warranty
MORTARA INSTRUMENT, INC. (hereinafter referred to as “Mortara”) hereby warrants that Mortara products
(hereinafter referred to as “Products”) shall be free from defects in material and workmanship under normal use,
service and maintenance for the warranty period of such Product from Mortara or an authorized distributor or
representative of Mortara. The warranty period is defined as twelve (12) months following the date of shipment
from Mortara. Normal use, service and maintenance means operation and maintenance in accordance with
appropriate instructions and/or information guides. This Warranty does not apply to damage to the Products caused
by any or all of the following circumstances or conditions:
a) Freight damage;
b) Parts and/or accessories of the Products not obtained from or approved by Mortara;
c) Misapplication, misuse, abuse and failure to follow the Product instruction sheets and/or information
guides;
d) Accident, a disaster affecting the Products;
e) Alterations or modifications to the Products not authorized by Mortara;
f) Other events outside of Mortara’s reasonable control or not arising under normal operating
conditions.
THE REMEDY UNDER THIS WARRANTY IS LIMITED TO THE REPAIR OR REPLACEMENT WITHOUT
CHARGE FOR LABOR OR MATERIALS, OR ANY PRODUCTS FOUND UPON EXAMINATION BY
MORTARA TO HAVE BEEN DEFECTIVE. This remedy shall be conditioned upon receipt of notice by Mortara
of any alleged defects promptly after discovery thereof within the warranty period. Mortara’s obligations under the
foregoing warranty will further be conditioned upon the assumption by the purchaser of the Products (i) of all
carrier charges with respect to any Products returned to Mortara’s principal place or any other place as specifically
designated by Mortara or an authorized distributor or representative of Mortara, and (ii) all risk of loss in transit. It
is expressly agreed that the liability of Mortara is limited and that Mortara does not function as an insurer. A
purchaser of a Product, by its acceptance and purchase thereof, acknowledges and agrees that Mortara is not liable
for loss, harm or damage due directly or indirectly to an occurrence or consequence therefrom relating to the
Products. If Mortara should be found liable to anyone under any theory (except the expressed warranty set forth
herein) for loss, harm or damage, the liability of Mortara shall be limited to the lesser of the actual loss, harm or
damage, or the original purchase price of the Product when sold.
EXCLUDED FROM THE LIMITED WARRANTY SET FORTH ABOVE ARE CONSUMABLE ITEMS SUCH
AS PAPER, BATTERIES, ELECTRODES, PATIENT CABLES, LEAD WIRES AND MAGNETIC STORAGE
MEDIUMS.
EXCEPT AS SET FORTH HEREIN WITH RESPECT TO REIMBURSEMENT OF LABOR CHARGES, A
PURCHASER’S SOLE EXCLUSIVE REMEDY AGAINST MORTARA FOR CLAIMS RELATING TO THE
PRODUCTS FOR ANY AND ALL LOSSES AND DAMAGES RESULTING FROM ANY CAUSE SHALL BE
THE REPAIR OR REPLACEMENT OF DEFECTIVE PRODUCTS TO THE EXTENT THAT THE DEFECT IS
NOTICED AND MORTARA IS NOTIFIED WITHIN THE WARRANTY PERIOD. IN NO EVENT,
INCLUDING THE CLAIM FOR NEGLIGENCE, SHALL MORTARA BE LIABLE FOR INCIDENTAL,
SPECIAL OR CONSEQUENTIAL DAMAGES, OR FOR ANY OTHER LOSS, DAMAGE OR EXPENSE OF
ANY KIND, INCLUDING LOSS OF PROFITS, WHETHER UNDER TORT, NEGLIGENCE OR STRICT
LIABILITY THEORIES OF LAW, OR OTHERWISE. THIS WARRANTY IS EXPRESSLY IN LIEU OF ANY
OTHER WARRANTIES, EXPRESS OR IMPLIED, INCLUDING, BUT NOT LIMITED TO THE IMPLIED
WARRANTY OF MERCHANTABILITY AND THE WARRANTY OF FITNESS FOR A PARTICULAR
PURPOSE.

iv
User Safety Information
Warning
Means there is the possibility of personal
injury to you or others.
Caution
Means there is the possibility of damage to
the equipment.
Note Provides information to further assist in the
use of the device.
Federal law restricts this device for sale to and use by or on the order
of a physician.
Warning
•Device (Ambulatory X12+) transmits data reflecting a patient’s physiological condition to a properly
equipped electrocardiograph and when reviewed by a trained physician or clinician can be useful in
determining a diagnosis. However, the data should not be used as a sole means for determining a patient’s
diagnosis.
•To maintain designed operator and patient safety, peripheral equipment and accessories used that can come
in direct patient contact, must be in compliance with UL 2601-1, IEC 601-1 and IEC 601-2-25.
•FCC Warning (Part 15.21): Changes or modifications not expressly approved by the party responsible for
compliance could void the user’s authority to operate the equipment.
•To maintain designed operator and patient safety, only use parts and accessories supplied with the device
and available through Mortara Instrument, Inc.
•To avoid the possibility of serious injury or death during patient defibrillation, do not come into contact
with device or patient cables. Additionally, proper placement of defibrillator paddles in relation to the
electrodes is required to minimize harm to the patient.
•A possible explosion hazard exists; do not use the device in the presence of flammable mixtures with air,
oxygen or nitrous oxide.
•Defibrillation protection is guaranteed only if the original patient cable is used.
•Simultaneous connection to other equipment may increase leakage current.
•Some stimulators may cause interference with the signal.
•ECG electrodes could cause skin irritation and should be examined daily. Reposition and change
electrodes every 24 hours, though it may be necessary to do so sooner if signs of irritation or inflammation
occur.
•Before attempting to use the device for clinical applications the operator must read and understand the
contents of the manual and any documents accompanying the device.

v
Caution(s)
•To prevent possible damage to the keypad, do not use sharp or hard objects to depress keys, only use
fingertips.
•Do not attempt to clean the device or patient cables by submersing into a liquid, autoclaving, or steam
cleaning.
•Wipe the exterior surface of the device and patient cables with a sterilizing disinfectant, and then dry with
a clean cloth.
•Conductive parts of the patient cable, electrodes and associated Type CF connections, including the neutral
conductor of the patient cable and electrode, should not come into contact with other conductive parts,
including earth ground.
•The Ambulatory X12+ and Patient Cable should be cleaned between each use.
•Do not pull or stretch patient cables as this could result in mechanical and/or electrical failures. Patient
cables should be stored after forming them into a loose loop.
•The Ambulatory X12+ will only work with electrocardiographs that are equipped with the appropriate
option.
•No user serviceable parts are inside. Any modification of this device may alter defibrillator protection.
Any modification to any part of this device is to be performed by qualified service personnel only.
•The following equipment may cause interference with the RF channel: microwave ovens, diathermy units
with LANs (spread spectrum), amateur radios and government radar.
•To prevent possible damage to the device during transport and storage (while in original packaging) the
following environmental conditions must be adhered to:
Ambient Temperature Range:
-20°C to 65°C (-4°F to 149°F)
Relative Humidity Range:
5% to 95% (non-condensing)
Atmosphere Pressure:
700 hPa to 1060 hPa
•Allow the device to stabilize within its intended operating environment for a minimum of two hours prior
to use. The allowable operating environment is as follows:
Ambient Temperature Range:
0°C to 45°C (32°F to 113°F)
Relative Humidity Range:
5% to 95% (non-condensing)
Atmosphere Pressure:
700 hPa to 1060 hPa

vi
Warning(s)
In some countries the use of the X12+ transmitter (2400 MHz version) has been limited as follows:
Spain: use is limited to channels in the range 8B to E6 (inclusive).
France: use is limited to channels in the range 8E to A5 (inclusive).
The channel setting of the X12+, when used in the above listed countries, must be set accordingly, as explained
in this manual at section 2.
FCC Compliance Statement
In the United States, use of the X12+ transmitters is regulated by Federal Communications Commission
(FCC).
FCC ID: HJR-X12-600-15
FCC ID: HJR-X12P-2500
These devices comply with Part 15 of the FCC rules.
Operation is subject to the following conditions:
1. This device may not cause harmful interference, and
2. This device must accept any interference received, including interference that may cause
undesired operation.
•The X12+ (600) must be used solely on the premises of health care facilities (see Part 15, section
15.242a).
•A health care facility operating the X12+ (600) must coordinate with the directors of existing
nearby TV stations and Radio Astronomy Observatories to ensure compatible use. Minimum
separation distances from such facilities may apply. It may be necessary to obtain written
authorization from such facilities prior to installation and use of the X12+ (Part 15, section
15.242d,e).
Industry Canada Compliance Statement
In Canada, use of the X12+ (600) transmitter is regulated by Industry Canada.
Canada ID: 3758104616
This device complies with RSS-210 of the Industry Canada rules.
This telemetry device is only permitted for installation in hospitals and health care facilities. Devices shall
not be operated in mobile vehicles (even ambulances and other vehicles associated with health care
facilities). The installer/user of this device shall ensure that it is at least 80 km from the Penticton radio
astronomy station (British Columbia latitude: 49o 19' 12" N, longitude: 118o 59'56" W). For medical
telemetry systems not meeting this 80 km separation (e.g. the Okinagan valley, British Columbia) the
installer/ user must coordinate with and obtain the written concurrence of the Director of the Penticton
radio astronomy station before the equipment can be installed or operated. The Penticton contact is
Tel: [phone]/ fax: [phone].

vii
Note
•Proper patient preparation is important to proper application of ECG electrodes and operation of the
device.
•Patient cables should be checked for cracks or breakage in their exterior properties prior to use.
•As defined by IEC 601-1 and IEC 601-2-25, the device is classified as follows:
- Internally powered
- Type CF applied parts
- Ordinary equipment
- Not suitable for use in the presence of flammable mixtures with air, oxygen or nitrous oxide
- Continuous operation
•The X12+ is a UL classified device:
Medical Equipment
WITH RESPECT TO ELECTRIC SHOCK,
FIRE, AND MECHANICAL HAZARDS ONLY,
IN ACCORDANCE WITH UL 60601-1,
CAN/CSA C22.2 No. 601.1, IEC60601-1 AND
IEC60601-2-25.
5P35
Equipment Symbols
Symbol Delineation
Attention, consult accompanying
documents
Attention, consult accompanying
documents.
Compliance with Directive 1999/5/EC
Defibrillator-proof type CF input
Battery

viii
Indicates compliance to applicable EEC
Directives
Electromagnetic Compatibility (EMC)
Electromagnetic compatibility with surrounding devices should be assessed when using the
X12+ Transmitter.
An electronic device can either generate or receive electromagnetic interference. Testing for electromagnetic
compatibility (EMC) has been performed on the X12+ Transmitter according to the international standard for EMC
for medical devices (IEC 60601-1-2). This IEC standard has been adopted in Europe as the European Norm (EN
60601-1-2).
The X12+ Transmitter should not be used adjacent to, or stacked on top of other equipment. If the X12+
Transmitter must be used adjacent to or stacked on top of other equipment, verify that the X12+ Transmitter
operates in an acceptable manner in the configuration in which it will be used.
Fixed, portable, and mobile radio frequency communications equipment can affect the performance of medical
equipment. See Table X-4 for recommended separation distances between the radio equipment and the X12+
Transmitter.
Accessories and Cables Warning
The use of accessories and cables other than those specified below, may result in increased emissions or decreased
immunity of the X12+ Transmitter.
Description Part Numbers
10-wire LeadForm Patient Cable/ Domestic
•Standard
•Large
10-wire LeadForm Patient Cable/ International
•Standard
•Large
9293-017-50
9293-026-50
9293-017-51
9293-026-51

ix
Table X-1 Guidance and Manufacturer’s Declaration: Electromagnetic Emissions
The X12+ Transmitter is intended for use in the electromagnetic environment specified in the table below. The
customer or the user of the X12+ Transmitter should assure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment: guidance
RF Emissions
CISPR 11
Group 2 The X12+ Transmitter must emit electromagnetic energy
in order to perform its intended function. Nearby
electronic equipment may be affected.
RF Emissions
CISPR 11
Class B
Harmonic
Emissions
IEC 61000-3-2
Not Applicable
Voltage
fluctuations/
flicker emissions
IEC 61000-3-3
Not Applicable
The X12+ Transmitter is suitable for use in all
establishments, including domestic establishments and
those directly connected to the public low-voltage power
supply network that supplies buildings used for
domestic purposes.

x
Table X-2 Guidance and Manufacturer’s Declaration: Electromagnetic Immunity
The X12+ Transmitter is intended for use in the electromagnetic environment specified below. The customer or the
user of the X12+ Transmitter should assure that it is used in such an environment.
Emissions Test Compliance Compliance
Level
Electromagnetic Environment:
guidance
Electrostatic
Discharge (ESD)
IEC 61000-4-2
+/- 6 kV contact
+/- 8 kV air
+/- 6 kV contact
+/- 8 kV air
Floors should be wood, concrete, or
ceramic tile. If floors are covered with
synthetic material, the relative humidity
should be at least 30%.
Electrical Fast
transient/burst
IEC 61000-4-4
+/- 2 kV for
power supply line
+/- 1 kV for
input/output lines
Not Applicable
Surge
IEC 61000-4-5
+/- 1 kV
differential mode
+/- 2 kV common
mode
Not Applicable
Voltage dips,
short
interruptions and
voltage variations
on
power supply
input
lines
IEC 61000-4-11
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
Not Applicable
Power frequency
(50./60 Hz)
magnetic field
3 A/m 3 A/m Power frequency magnetic fields should
be at levels characteristic of a typical
location in a typical commercial or
hospital environment.
Note: UT is the a.c. mains voltage prior to application of the test level.

xi
Table X-3 Guidance and Manufacturer’s Declaration: Electromagnetic Immunity
The X12+ Transmitter is intended for use in the electromagnetic environment specified below. The customer or the
user of the X12+ Transmitter should assure that it is used in such an environment.
Emissions Test IEC 60601
Test Level
Compliance
Level
Electromagnetic Environment: guidance
Conducted RF
IEC 61000-4-6
3 Vrms
150 kHz to
80 MHz
3 Vrms
150 kHz to
80 MHz
Radiated RF
IEC 61000-4-3
3 Vrms
80 MHz to
2.5 GHz
3 Vrms
80 MHz to
2.5 GHz
Portable and mobile RF communications
equipment should be used no closer to any part of
the X12+ Transmitter, including cables, than the
recommended separation distance calculated
from the equation applicable to the frequency of
the transmitter.
Recommended separation distance
P
Vrms
d





=
3
5.3
P
mV
d





=
/3
5.3 80 MHz to 800 MHz
P
mV
d





=
/3
7800 MHz to 2.5 GHz
Where P is the maximum output power rating of
the transmitter in watts (W) according to the
transmitter manufacturer and d is the
recommended separation distance in meters (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site surveya,
should be less than the compliance level in each
frequency rangeb.
Interference may occur in the vicinity of
equipment marked with the following symbol:
a. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radios, amateur radios, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with
accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey
should be considered. If the measured field strength in the location in which the X12+ Transmitter is used exceeds
the applicable RF compliance level above, the X12+ Transmitter should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the
X12+ Transmitter.
b. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than [3] V/m.

xii
Table X-4 Recommended Separation Distances Between Portable and Mobile RF
Communications Equipment and the X12+ Transmitter.
The X12+ Transmitter is intended for use in the electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the X12+ Transmitter can help to prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the
X12+ Transmitter as recommended below, according to the maximum output power of the communications
equipment.
Rated
Maximum
Output Power of
Transmitter W
Separation Distance According to Frequency
of
Transmitter (m)
150 KHz to 800 MHz 800 MHz to 2.5 GHz
Pd 2.1=Pd 3.2=
0.01 0.1 m 0.2 m
0.1 0.4 m 0.7 m
1 1.2 m 2.3 m
10 4.0 m 7.0 m
100 12.0 m 23.0 m
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in
meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 800 MHz, the separation distance for the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by the absorption
and reflection from structures, objects, and people.

xiii
Table of Contents
1 Introduction
Manual Purpose ..............................................................................................................................................1-1
Audience..........................................................................................................................................................1-1
System Description..........................................................................................................................................1-1
Equipment Included.........................................................................................................................................1-1
X12+ Front View ..............................................................................................................................................1-2
LeadForm Patient Cable..................................................................................................................................1-2
X12+ Transmitter in Carrying Pouch ...............................................................................................................1-3
X12+ Ambulatory Transmitter Part Numbers ..................................................................................................1-4
Supplies Contact .............................................................................................................................................1-4
Ambulatory X12+ Specifications......................................................................................................................1-5
Operation
2
Read Instructions ............................................................................................................................................2-1
Battery Installation/Removal/Battery Door .....................................................................................................2-2
Turning the Ambulatory X12+ ON ..................................................................................................................2-3
Turning the Ambulatory X12+ OFF ................................................................................................................2-3
LCD Display Battery Voltage Indicator ...........................................................................................................2-3
Attaching the Patient Cable ............................................................................................................................2-4
Patient Hook-Up .............................................................................................................................................2-4
Skin Preparation ................................................................................................................................2-4
Positioning the Electrodes .................................................................................................................2-5
Using the Keypad ...........................................................................................................................................2-6
Main Menu ......................................................................................................................................................2-6
Top Level Menu Options ................................................................................................................................2-7
Lead Check ....................................................................................................................................................2-8
Checking Impedances ....................................................................................................................................2-8
Displaying ECG Leads ...................................................................................................................................2-9
Configuring the Ambulatory X12+ Transmitter ...............................................................................................2-9
Setting the Transmission Channel Number ......................................................................................2-11
Setting the Number of Patient Cable Leadwires ...............................................................................2-11
Setting Language ..............................................................................................................................2-12
Viewing Software Version Number ....................................................................................................2-12
Viewing Battery Voltage ....................................................................................................................2-12
Starting a Patient Transmission Session ........................................................................................................2-12
Sending (Optional) Call Signals .....................................................................................................................2-13
Ending a Transmission Session .....................................................................................................................2-13
3 Maintenance
Cleaning the Ambulatory X12+ Transmitter and Patient Cable ......................................................................3-1
Periodic Maintenance ......................................................................................................................................3-1
Disposal of Waste Material..............................................................................................................................3-1

xiv
Appendix Messages and Information
A
Table of Messages ..........................................................................................................................................A-1
System Information Log...................................................................................................................................A-2
Serial Number and Part Number Location ......................................................................................................A-3
Appendix Channel Assignments
B
600MHz ...........................................................................................................................................................B-1
2500MHz .........................................................................................................................................................B-2
Appendix Translations
C
Table of Translations .......................................................................................................................................C-1
Glossary ..................................................................................................................................................G-1
Index ...........................................................................................................................................................I-1

_____________________________________________________________________Section 1
1-1
1 Introduction
X12+ Overview
Manual Purpose
The X12+ User Manual explains how to operate the Ambulatory X12+ Transmitter. It shows how to
•Acquire and transmit 12-Lead ECG signals to a receiving device
•Setup device configurations
Audience
This manual is written for clinical professionals who are expected to have a working knowledge of medical
procedures and terminology as required for monitoring cardiac patients.
Conventions
Keys, such as Enter, appear in bold Arial font.
Text on the LCD screen of the X12+ appears in regular Arial font.
System Description
The Mortara Instrument Ambulatory X12+ Telemetry Module represents the state-of-the-art in Wireless
Electrocardiographic Technology. It provides a means to acquire and transmit 12-lead cardiac signals without
direct connections to an electrocardiograph. Design innovations implemented in the X12+ Telemetry Module
achieve real-time acquisition, RF transmission of simultaneous 12-lead ECG data with diagnostic quality to the
Mortara Receiver Module while allowing the patient to be ambulatory.
In addition, by using a very high monitoring frequency to transmit cardiac signals, the diagnostic bandwidth of
the signals is maintained.
The Ambulatory X12+ affords the patient complete freedom of movement. Unlimited range can also be
obtained with addition of the Mortara Antenna Network Box(s).
The X12+ Transmitter uses a single AA alkaline battery.
Equipment Included
The following equipment is necessary to use the Ambulatory X12+ Telemetry Module:
•Ambulatory X12+ (transmitter),
•One AA battery, 1.5V,
•Mortara Receiver Module with Antennas,
•Patient cable
•Antenna Network (optional)

X12+_________________________________________________________________________
1-2
X12+ Transmitter with Patient Cable
Front View, Figure 1-1
LeadForm Patient Cable, Figure 1-2
Patient Cable

_____________________________________________________________________Section 1
1-3
X12+ Transmitter in Carrying Pouch, Figure 1-3
Carrying Pouch
with Neck Strap

X12+_________________________________________________________________________
1-4
Mortara Part Numbers/ X12+ Ambulatory Transmitter
X12+ Transmitter
Description Part Numbers
X12+ Transmitter
X12+ Battery Door
X12+ Carrying Pouch with Belt and Neck Strap
10-wire LeadForm Patient Cable/ Domestic
•Standard
•Large
10-wire LeadForm Patient Cable/ International
•Standard
•Large
X12+ User Manual / English
X12+ Short Form Instruction Card / English
Monitoring Hook-up Kit
•10 Monitoring Electrodes
•1 Abrasive Pad
•1 4x4 Gauze wipe
•1 Razor
•2 Alcohol Prep Pads
X12PLUS-XXX-XXXXX
8346-003-50
8485-020-50
9293-017-50
9293-026-50
9293-017-51
9293-026-51
9515-164-50-ENG
NEW
9294-009-50
To order additional supplies, contact a Mortara Instrument customer service representative at:
Mortara Instrument, Inc.
7865 N. 86th Street
Milwaukee, WI 53224
Phone: 1-888-MORTARA (667-8272)
Fax: [phone]
Internet: http://www.mortara.com