Manual WatchPAT 200

WatchPAT™200 Unified
Operation Manual
Itamar Medical REF OM2196335
Caution: Federal (U.S.) law restricts this device to sale by, or on the order of, a
physician. Not for pediatric use.
Copyright  2015 By Itamar Medical Ltd.

WatchPAT™ and PAT® are trademarks of Itamar Medical, Ltd.
This manual and the information contained herein are confidential and are the sole property
of Itamar Medical Ltd. Only Itamar Medical Ltd. or its licensees have the right to use
this information. Any unauthorized use, disclosure or reproduction is a direct violation of
Itamar Medical’s proprietary rights.
DISCLAIMER
Itamar Medical Ltd. shall not be held responsible in any manner for any bodily injury
and/or property damage arising from operation or use of this WatchPAT™200 Unified
other than that which adheres strictly to the instructions and safety precautions contained
herein and in all supplements hereto and according to the terms of the warranty provided in
the License Agreement in Appendix C.
Itamar Medical Ltd.

9 Halamish St., P.O. Box 3579
Caesarea Ind. Park, 3088900, Israel
Tel: International + 972-4-617-7000, US 1-888-7ITAMAR
Fax + 972 4 627 5598
www.itamar-medical.com
This product and/or method of use, is covered by one or more of the following US patents: 6319205,
6322515, 6461305, 6488633, 6916289, 6939304, 7374540, as well as any pending US patent applications and
corresponding patents and/or applications filed in other countries.
ISO 9001:2008 and EN ISO 13485:2012

See appendix D for contact information of the regulatory authorized representative
WatchPAT™200U System i Operation Manual

Record of Editions
Edition Date Description Chapter Pages Resp.

1 (based on Oct 2015  ARMS – correcting App.G 64 Orit
OM2196331 Ed.6 typo
and Ed.7)
Note: Latest version of the WatchPAT™ system Operation Manual is available at:
http://www.itamar-medical.com/Support/Downloads.html
WatchPAT™200U System ii Operation Manual

Table of Contents
1 GENERAL INFORMATION ..................................................... 1

1.1 Intended Use / Indications for Use ........................................................ 1
1.2 Restrictions for Use ................................................................................ 1
1.3 Exclusion Criteria.................................................................................... 2
1.4 Data Generated by the WatchPAT™200U ............................................. 2
1.5 Equipment Classification ....................................................................... 2
1.6 Quality Assurance System: ISO 9001 & EN ISO 13485 ........................ 3
1.7 CE and CSA Compliance ........................................................................ 4
1.8 Conventions Used in this Manual .......................................................... 4
1.9 Warnings, Cautions and Notes .............................................................. 5
1.10 Safety Precautions .................................................................................. 6
1.11 Symbols Used on the Product Labels ................................................... 7
1.12 WatchPAT™200U Device Labels ........................................................... 8
1.13 FDA information ...................................................................................... 8
2 OVERVIEW ............................................................................. 9
2.1 System Description............................................................................... 10
2.2 User Interaction with the WatchPAT™ Device Keys .......................... 11
2.3 WatchPAT™ Device Function .............................................................. 13
2.4 Built-In Self-Diagnostic Procedures .................................................... 14
3 PREPARATION FOR SLEEP STUDY ...................................18
3.1 Charging the Battery............................................................................. 18
3.2 Preparing the Snore and Body Position Sensor ................................ 19
3.3 Preparing the Wrist Strap ..................................................................... 19
3.4 Mounting the WatchPAT™ on the Wrist Strap ................................... 20
3.5 Replacing the uPAT Probe ................................................................... 20
3.6 Preparing the WatchPAT™ Device for a New Study .......................... 21
3.7 Testing the WatchPAT™ Device .......................................................... 21
3.8 WP200U Self-diagnostic Test Results and Trouble-shooting ........... 21
3.9 Packing the Carrying Case ................................................................... 22
4 OPTIONAL FUNCTIONS .......................................................23
4.1 Using the integrated Snore & Body Position Sensor......................... 23
4.2 Tamper-Proof Testing with WatchPAT™ Device ................................ 23
4.3 Multi-night study ................................................................................... 26
5 DATA DOWNLOAD AND ANALYSIS ...................................27
6 MAINTENANCE .....................................................................28
6.1 Cleaning ................................................................................................. 28
WatchPAT™200U System iii Operation Manual

6.2 Handling................................................................................................. 29
6.3 Replacing the uPAT Probe Cable ........................................................ 29
6.4 Replacing the Battery ........................................................................... 30
6.5 Setting the Time and Date of the WatchPAT™ device ....................... 31
6.6 Storing the WatchPAT™ device........................................................... 32
7 APPLYING THE WATCHPAT™ DEVICE ..............................33
7.1 Preparing for Use of the WatchPAT™ Device .................................... 33
7.2 Applying the WatchPAT™ Device ....................................................... 33
7.3 Attaching the uPAT Probe .................................................................... 34
7.4 Switching On the WatchPAT™ device ................................................ 36
7.5 When You Wake Up .............................................................................. 36
7.6 Important Notes..................................................................................... 37
8 PATIENT TRAINING – GUIDELINES ...................................38
8.1 Walk Through the Process of Using the WatchPAT™ device ........... 38
8.2 Product Introduction............................................................................. 38
8.3 Applying the WatchPAT™ device ........................................................ 38
8.4 Switching on the WatchPAT™ Device ................................................ 39
8.5 Removing the WatchPAT™ Device ..................................................... 39
8.6 Patient Training ..................................................................................... 39
8.7 Review Safety, General and Functional Issues .................................. 39
9 TROUBLESHOOTING GUIDE ...............................................40
9.1 Operator Error Messages ..................................................................... 40
9.2 Patient Error Messages ........................................................................ 41
10 SPECIFICATIONS .................................................................42
APPENDIX A: WP200U INTEGRATED SNORING + BODY
POSITIONING SENSOR OPERATING INSTRUCTIONS ..................43
APPENDIX B: TAMPER-PROOF TESTING WITH
WATCHPAT™200U ...........................................................................48
APPENDIX C: LICENSE AGREEMENT ...........................................52
APPENDIX D: REGULATORY REPRESENTATIVE ........................58
APPENDIX E: DESCRIPTION OF THE WATCHPAT™200U UPAT
PROBE ...............................................................................................59
APPENDIX F: MANUFACTURING DECLARATIONS ACCORDING
TO IEC 60601-1-2 ...............................................................................60
APPENDIX G: SPO2 ACCURACY IN THE WATCHPAT™200U ......64
WatchPAT™200U System iv Operation Manual

APPENDIX H: TRAINING RESOURCES ..........................................67
APPENDIX I: SPARE PARTS LIST ...................................................68
List of Figures
Figure 1 – Packed Device ................................................................................... 11
Figure 2 – WatchPAT™200U Device with Sensors ........................................... 11
Figure 3 – The Buttons and Display .................................................................. 12
Figure 4 – Service Ports and Peripherals .......................................................... 13
Figure 5 – WatchPAT™ Wrist Strap ................................................................... 13
Figure 6 – Charging the WatchPAT™ Device ................................................... 18
Figure 7 – Disconnecting the Probe .................................................................. 20
Figure 8 – Probe Disconnected .......................................................................... 20
Figure 9 – WatchPAT™ Fully Prepared ............................................................. 21
Figure 10 – WatchPAT™ Device with Tamper-Proof Bracelet ......................... 24
Figure 11 – Bracelet on Patient's Hand ............................................................. 24
Figure 12 – WatchPAT™ Device with Cable for Bracelet ................................ 25
Figure 13 – WatchPAT™ Device with Bracelet ................................................. 25
Figure 14 – Bracelet and WatchPAT™ Device on a Patient’s Hand ................ 25
Figure 15 – Cut the Bracelet on a Specified Location ...................................... 25
Figure 16 – Case for 3 Night Multi-night Study ................................................. 26
Figure 17 – uPAT Probe Cable with Screw........................................................ 29
Figure 18 – Replacing the uPAT Probe ............................................................. 30
Figure 19 – Replacing the Battery...................................................................... 31
Figure 20 – Finger Designation .......................................................................... 33
Figure 21 – Putting On The Wrist Strap ............................................................. 34
Figure 22 – Wearing the WatchPAT™ Device ................................................... 34
Figure 23 – Placing Finger In uPAT Probe ........................................................ 35
Figure 24 – Removing TOP Tab ......................................................................... 35
Figure 25 – Wearing the WP200U – Ready for Sleep ........................................ 35
List of Tables
Table 1 – Operator Troubleshooting .................................................................. 40
Table 2 – Patient Troubleshooting ..................................................................... 41
Table 3 – WatchPAT™200U Specifications ....................................................... 42
WatchPAT™200U System v Operation Manual

1 GENERAL INFORMATION
This manual is part of the WatchPAT™200 Unified system.
1.1 Intended Use / Indications for Use

The WatchPAT™200U (WP200U) device is a non-invasive home care device for use with
patients suspected to have sleep related breathing disorders. The WP200U is a diagnostic
aid for the detection of sleep related breathing disorders, sleep staging (Rapid Eye
Movement (REM) Sleep, Light Sleep, Deep Sleep and Wake), snoring level and body
position. The WP200U generates a peripheral arterial tonometry ("PAT") Respiratory
Disturbance Index ("PRDI"), Apnea-Hypopnea index ("PAHI"), PAT sleep staging
identification (PSTAGES) and optional snoring level and body position discrete states from
an external integrated snoring and body position (SBP) sensor. The WP200U's PSTAGES
and SBP provide supplemental information to its PRDI/PAHI. The WP200U's PSTAGES
and SBP are not intended to be used as the sole or primary basis for diagnosing any sleep
related breathing disorder, prescribing treatment, or determining whether additional
diagnostic assessment is warranted.
The WatchPAT™200U device is not indicated for children less than 12 years old.
1.2 Restrictions for Use

1. The WP200U should be used only in accordance with physician’s instructions. For
exclusion criteria see Section ‎1.3.
2. Only qualified medical personnel may authorize the use of the WP200U.
3. Qualified medical personnel must instruct the patients (and accompanying
individual if needed) how to attach and use the WP200U prior to use.
4. In the event of equipment malfunction all repairs should be executed by authorized
Itamar Medical Ltd. personnel or licensed service agents.
5. The eligibility of a patient for a PAT® study is entirely at the discretion of a
physician, and is generally based upon the patient’s medical status.
6. The WP200U system in whole, or in part, may not be modified in any way.
7. The WP200U is used as an aid for diagnostic purposes only, and should not be used
for monitoring.
8. Only suitably trained and qualified personnel should be authorized to prepare the
WP200U equipment prior to use.
9. The WP200U Operation Manual should be carefully studied by the authorized
operators, and kept where it is easily accessible. Periodic review of the Manual is
recommended.
10. Itamar Medical Ltd. makes no representation whatsoever, that the act of reading the
Manual renders the reader qualified to operate, test or calibrate the system.
11. The tracings and calculations provided by the WP200U system are intended as tools
for the competent diagnostician. They are explicitly not to be regarded as a sole
incontrovertible basis for clinical diagnosis.
WatchPAT™200U System 1 Operation Manual

12. In the event that the system does not operate properly, or if it fails to respond to the
controls in the manner described in this Manual, the operator should refer to the
Troubleshooting section. If necessary, contact our service office to report the
incident, and to receive further instructions.
13. The step by step instructions for the patient should be carefully followed when
attaching the unit to the patient.
14. The WP200U is not indicated for children less than 12 years old.
1.3 Exclusion Criteria

The WatchPAT™200U should not be used in the following cases:
1. Use of one of the following medications: alpha blockers, short acting nitrates (less
than 3 hours before the study).
2. Permanent pacemaker: atrial pacing or VVI without sinus rhythm.
3. Sustained* non-sinus cardiac arrhythmias.
* In cases of patient having accumulative time of regular R-R intervals of less than 1.5
hours, the WatchPAT™200U system will not have sufficient valid PAT® signal as required
to generate a sleep report.
1.4 Data Generated by the WatchPAT™200U

The WatchPAT™200U generates a PAT respiratory disturbance index (“PRDI”) and its
derivative, the PAT Apnea-Hypopnea Index (“PAHI”) and PAT sleep staging identification
("PSTAGES"). The PAHI and PRDI are estimates of conventional RDI and AHI values and
REM, DEEP SLEEP, LIGHT SLEEP, and WAKE stages identification that are produced
by polysomnography (“PSG”). The WatchPAT™200U also generates optional acoustic
decibel detector used for snoring level and body position discrete states from an external
integrated snoring and body position (SBP) sensor.
1.5 Equipment Classification

The WP200U is a Class IIa medical device under MDD 93/42 EEC: 1993 & Amm.
2007/47/EC Annex IX rule 10.

1.6 Quality Assurance System: ISO 9001 & EN ISO 13485
The Itamar Medical WP200U is compliant to the following standards.
STANDARD #
1. Medical electrical equipment – Part 1: General requirements IEC 60601-1
for basic safety and essential performance
2. Medical electrical equipment – Part 1-2: General IEC 60601-1-2
requirements for basic safety and essential performance -
Collateral standard: Electromagnetic compatibility -
Requirements and tests
3. Medical Device Software – Software Life Cycle Processes IEC 62304
4. Medical electrical equipment - Part 1-4: General IEC 60601-1-4
requirements for safety – Collateral Standard:
Programmable electrical medical systems
5. Medical electrical equipment -- Part 1-11: General IEC 60601-1-11
requirements for basic safety and essential performance --
Collateral standard: Requirements for medical electrical
equipment and medical electrical systems used in the home
healthcare environment
6. Degrees of protection provided by enclosures (IP Code) – IEC 60529
IP22
7. Quality management systems - requirements ISO 9001:2008
8. Medical devices. Quality management systems. EN ISO 13485:2012
Requirements for regulatory purposes
9. Medical devices - Quality management systems - CAN/CSA-ISO
Requirements for regulatory purposes (Health Canada) 13485:2003
10. Medical devices. Application of risk management to ISO 14971
medical devices
11. Medical devices. Symbols to be used with medical device ISO 15223-1
labels, labelling and information to be supplied. General
requirements
12. Symbols for use in the labelling of medical devices EN 980
13. Graphical symbols for electrical equipment in medical IEC TR 60878
practice
14. Graphical symbols - Safety colours and safety signs -- ISO 7010-M002
Registered safety signs; refer to instruction manual/ booklet
15. Information supplied by the manufacture with medical EN 1041
devices
16. Biological evaluation of medical devices - Part 1: ISO 10993-1
Evaluation and testing
17. Medical devices - Application of usability engineering to BS EN 62366
medical devices

18. Medical Device Directive MDD 93/42 EEC
MDD 2007/47/EC
19. FDA Quality Systems Regulation (QSR) 21 CFR part 820
20. UL standard for safety UL 60601-1
21. CSA Standard for safety CSA 22.2 No.601.1
22. Canadian Medical Devices Regulation SOR/98-282
23. Medical electrical equipment - Part 2-61: Particular ISO 80601-2-61
requirements for basic safety and essential performance of
pulse oximeter equipment
1.7 CE and CSA Compliance
The product complies with MDD 93/42 EEC: 1993 &

Amm. 2007/47/EC (Medical Device Directive)
requirements and CE approved.
The product is marked with the CE logo.
The product is certified by CSA.
1.8 Conventions Used in this Manual

Note: Throughout this document, the references WatchPAT™, WatchPAT™200U and
WP200U device are used to refer to the WatchPAT™200 Unified device.
Warnings are used to identify conditions or actions, which - if the

instructions are ignored - may violate patient safety, or cause
damage/malfunction to the system, resulting in non recoverable loss of
data.
Les avertissements sont utilises pour identifier les conditions ou les

actions qui- si elles sont ignorées- peuvent porter atteinte à la sécurité
des patients ou causer des dommages au système et résulter à une
perte irréversible des données.

Cautions are used to identify conditions or actions, which could cause
interference with data acquisition and/or impair study results.
Les précautions sont utilisées affin d’identifier les conditions ou les

actions qui peuvent interférer avec le ramassage de données et
provoquer des résultats équivoque.
Notes are used to identify an explanation, or to provide additional

information for purposes of clarification.
Les notes sont utilisées pour identifier les explications et pour donner des
informations supplémentaires dans le but de clarifier.
1.9 Warnings, Cautions and Notes

The WP200U is internally powered from a 4.2 V battery.
The WP200U is portable with continuous operation.
The WP200U uses BF patient applied parts.
The WP200U uses UL listed power supply (USA & Canada only).
The power supply is used in a non-patient environment only.
The WP200U should only be transported in its original case.
There are no serviceable parts inside the WP200U.
Environmental conditions during transportation & storage: See Specifications section.
Environmental conditions during operation: See Specifications section.
Sleep professionals (other than patients) using the WP200U should read the Operation
Manual.

1.10 Safety Precautions
WARNINGS
Use only the AC adapter provided (5V DC, 5W maximum capacity power
supply). Only authorized personnel may charge the WP200U. Failure to heed
this warning may cause permanent damage to the equipment.
Do not let the unit get wet.
Avoid placing food or water on any part of the system.
In the event of fire use only fire extinguishers approved for use on electrical
fires.
Handle unit with care. This unit is sensitive to extreme movements and to
falling.
Do not attempt to connect or disconnect any part of the unit.
Do not try to introduce any foreign object into the unit.
The WP200U MUST be charged ONLY after being removed from the
patient!
The WP200U MUST be removed from the patient BEFORE connecting it to
a PC!
AVERTISSEMENTS
Utiliser seulement un 5V DC, 5W alimentation d'énergie. Seul les techniciens
autorisés peuvent charger la montre PAT. Ignorer cet avertissement peut
causer des dommages irréparables a l’équipement. Ne pas mouiller l’unité.
L’unité est sensible au mouvement extrême est à la chute. L’utiliser avec
précaution. Ne pas essayer de brancher ou débrancher une des parties de
l’unité.
Ne pas introduire un objet étranger a l’intérieur de l’unité.
Le système WP200U doit être rechargé uniquement après avoir été retiré de
la main du patient.
Il est impératif de retirer le système WP200U de la main du patient avant de le
relier a l'ordinateur pour faire fonctioner les programmes.

1.11 Symbols Used on the Product Labels
Follow instructions for use
Type BF applied part
The product is certified by CSA
The product is marked with the CE logo

0473 for Intertek
Date of manufacture
2015
3.7V DC
Battery Operating Voltage
Single use, do not re-use
Temperature limit
Use-by date
Medical device Manufacturer
Catalogue Number
Serial Number
IP22 Ingress protection

The device is protected against insertion of fingers and vertically
dripping water shall have no harmful effect when the device is tilted
at an angle up to 15° from its normal position

Authorized representative in the European Community
1.12 WatchPAT™200U Device Labels
Located on WatchPAT™200U device
Located on WatchPAT™200U device
1.13 FDA information

The WatchPAT200U is cleared by the FDA under K133859, trade name Watch-PAT
200U (WP200U).

2 OVERVIEW
Obstructive sleep apnea syndrome (OSAS) is considered a major public health problem.
The prevalence of the syndrome is estimated at 2% to 5% in the adult population. It is
characterized by recurrent events of complete or partial obstruction of the upper airways
during sleep, often leading to hypoxemia, and/or arousals associated with sympathetic
nervous system activation. The diagnosis and assessment of the sleep apnea patient is based
on the Respiratory Disturbance Index (RDI), the number of Apneas, Hypopneas and
Respiratory Effort Related Arousals (RERA) per hour of sleep, along with sleep
architecture. The common consequences of this sleep disruption are daytime sleepiness,
poor daytime performance and increased vulnerability to accidents. Cardiovascular
complications such as systemic/pulmonary hypertension, ischemic heart disease and
arrhythmias are the major sequel of OSAS in the adult population.
The WP200U is worn on the wrist and is utilizing a plethysmographic based finger–
mounted probe that measures the PAT® (Peripheral Arterial Tone) signal. The PAT® signal
is a measurement of the pulsatile volume changes in the fingertip arteries which reflects the
relative state of the arterial vasomotor activity, and thus indirectly the level of sympathetic
activation. Peripheral arterial vasoconstriction, which mirrors sympathetic activation, is
shown as attenuation in the PAT® signal amplitude.
The same probe measures RED and IR channels used for the measurement of SpO2 signal.
The PAT®and SpO2 signals are recorded continuously and stored on an embedded micro
SD card, together with data from a built-in actigraph (embedded in the WP200U).
Following the sleep study, the recordings are automatically downloaded and analyzed in an
offline procedure using the proprietary zzzPAT software.
The zzzPAT algorithms use the four WP200U channels (PAT®, Pulse Rate, Oxygen
saturation and actigraphy) for the detection of sleep related breathing disorders and sleep
staging (Rapid Eye Movement (REM), Light Sleep, Deep Sleep and Wake). The zzzPAT
uses WP200U's snoring and body position channels (SBP) to generate snoring level and
body position discrete states. The use of SBP is optional and according to physician
preference.
The software issues comprehensive reports of the study, with statistics and graphic
presentation of the results. The whole night data can be viewed and the automatically
detected events can be revised manually.

2.1 System Description
The WP200U system is comprised of the following items:
 WP200U device that includes:
o Embedded actigraph
o Embedded pulse oximeter
o Embedded CPU and electrical circuit card
o Embedded micro SD card drive
o Rechargeable Lithium Ion Battery
o LCD display
 uPAT probe (includes oximetry)
 uPAT probe connection cable
 Wrist Strap
 Snore and Body Position sensor – optional
 Cable for Tamper-Proof Bracelet – optional
 Tamper-Proof Bracelet - optional
 AC adapter
 USB cable
 Step-by-Step Reference Guide (to be used in conjunction with Section 7)
 Quick Reference Cards (to be used in conjunction with Section 8)
 Carrying case

Figure 1 – Packed Device
Optional Snore & Body

Position sensor
uPAT probe
Figure 2 – WatchPAT™200U Device with Sensors
An additional item required for the operation of the system is the zzzPAT kit. zzzPAT is a
proprietary PC software for initializing the study, retrieving, analyzing and displaying the
data. For more information, refer to the zzzPAT Operation Manual.
2.2 User Interaction with the WatchPAT™ Device Keys

The WatchPAT™ has the following keys (see Figure 3):

 Central On/Enter key to power on the WatchPAT™ (the only key
visible to the patient)
 Outer ring containing four keys (left, right, up, down) that may be used
by the Operator for entering the diagnostic mode and navigating
through the diagnostic menu. These keys are hidden from the patient.
UP
LCD
RIGHT
ON/ENTER
DOWN
LEFT
Figure 3 – The Buttons and Display
LCD Display
The display is used for reading status and error messages. The display is divided
to three sections: Title, Info and Status.
 Title (first line): Current operational mode and time
o PATIENT mode while recording night study
o DIAGNOSTIC mode while testing device
o PC HOST while connecting to PC
o CHARGER mode while connecting to AC adapter
 Info (2nd-5th line): Specific information depending on
operational mode
 Status (last line): Message indicating device status depending
on operational mode
Service Ports and Peripherals

The WatchPAT™ device has 4 ports that are used either for sensor connections
or for servicing and charging (see Figure 4).
 The bracelet port is used for connecting the tamper-proof
bracelet.
 The uPAT probe port is used for connecting the uPAT probe

 A port for connecting the optional Snore & Body Position
sensor
 The USB port is used for charging or connecting to the PC
uPAT probe port
Bracelet port
Port for optional Snore
& Body Position
sensor
USB port for charging

and communication
Figure 4 – Service Ports and Peripherals
Wrist strap
Figure 5 – WatchPAT™ Wrist Strap
2.3 WatchPAT™ Device Function

The WatchPAT™ records the following channels:
 PAT® Signal
 Oxygen saturation

 Actigraphy (movement)
 Acoustic decibel detector for Snoring evaluation (optional)
 Body Position (optional)
The overnight sleep study data is stored on an embedded micro SD card in the
WatchPAT™ device. After the study is recorded, the data is downloaded from the
WatchPAT™ device through the USB cable using the zzzPAT software. The zzzPAT
software, utilizing automatic algorithms, detects respiratory and other events that occurred
during sleep as well as periods of REM, deep sleep, light sleep and wakefulness. The pulse
rate signal is derived from the PAT® signal and used in the automatic analysis. The
software issues comprehensive detailed reports of the study. The whole night data can be
viewed on the PC screen and the automatically detected events can be revised manually.
An optional tamper-proof patient identification function is available using a custom

bracelet whose presence during the night verifies that the identified patient is indeed the
one sleeping with the device (see Tamper-Proof Testing with WatchPAT™ Device
Tamper-Proof Testing with section).
The patient normally sleeps only one night with the WatchPAT™ device unless an optional
multi-night option is selected which enables an up to 3 nights study with the same device
(see Multi-night study section).
2.4 Built-In Self-Diagnostic Procedures

2.4.1 Operator Tests
The WatchPAT™200 unified contains a comprehensive built-in self-diagnostic procedure.
This procedure is available to the operator and hidden from the patient. The procedure can
be accessed if the UP and DOWN keys (see Figure 3) are pressed simultaneously after the
device is powered ON (during the first 30 seconds only after the device is powered ON).
The procedure performs the following test:
 Device Test – tests the WatchPAT™ for errors before performing a night study
(make sure all sensors are connected before initiating this test)
Note
In all times, the current time is shown in the upper right hand corner of the
LCD display.
To run the self-diagnostic procedure:

 Press the ENTER button (Center key) for 2 seconds till the Itamar medical logo
appears on the LCD screen
 Immediately press the UP + DOWN keys (see Figure 3) simultaneously for 1
second

The following screen will be displayed:
DIAGNOSTIC 22:40
2.2140 20-Jul-08
*device test (30001)
end testing
Select test ↑↓
 First line displays title and current time

 Second line displays current embedded S/W version (2.2139) and current date
 Third line displays option for running device test (serial number of device in
parenthesis)
 Fifth line indicates option for end testing (turn device off). If no test is selected
within 3 minutes the WatchPAT™ device will automatically shut down
 The Up, Down keys (↑↓) navigate between the lines.
 An asterisk will indicate current selection. When moving the ↑↓ keys, the asterisk
will move to indicate the current selection. Press the central Enter key to make the
desired selection.
It is recommended that you perform the Device every time you prepare the WatchPAT™
for a night study.
2.4.2 Device Test

At the completion of the device test, a TEST PASSED indicates that the device is ready
for the night study.
DEVICE TEST 22:50

ID=111-11-1111
sbp=missing
<-Back
TEST PASSED 2:54
At the completion of the device test, a TEST FAILED indicates a problem that should be
taken care of before the device is released for a night study.
DEVICE TEST 22:50

ID=111-11-1111
pat=missing

<-Back More->
TEST FAILED 2:54
The following are the possible error, warning or information messages:
 File error: not loaded, missing – the study file was not loaded or somehow
the file was deleted
 File error: used x/3 x=1..3 – only when multi-night option is selected
 Battery error: low – needs charging
 Probe error: used, missing, bad – connect an unused probe
 Hardware (H/W) error: error code - contact customer support
 SBP (Snore and Body Position sensor) warning: sensor missing – does not
affect PASSED status
 RTC (Real Time Clock) warning: faulty – indicates problem with internal
clock but does not affect PASSED status
 Bracelet error: missing – the study file was chosen with the bracelet option
but the bracelet is not connected during the device test
 Information messages:
o multi-night=on - when a multi night study is required
o bracelet=on - when a study with tamper-proof patient
identification bracelet is required
More-> indicates that there are more error/warning messages and will be displayed if the
Right (->) button is pressed.
<-Back will move to the previous screen if the Left (<-) button is pressed.
2.4.3 Patient Test

When the patient (and accompanying individual if needed), turns on the WatchPAT™
device by pushing the On/Enter key (center button) for about 2 seconds a self-diagnostic
test is automatically performed and the following screen is displayed:
PATIENT 22:51
Please wait
Testing…
If the WatchPAT™ device passes this self-diagnostic test, the following screen will be
displayed:
PATIENT 22:51
GOOD NIGHT!!!

Time elapsed=9:50
Recording…
Note
During recording the LCD display turns off to conserve battery life. Any
key pressed during Recording will turn on the LCD for 30 seconds.
If the WatchPAT™ device fails this self-diagnostic test, the following screen will be
displayed:
PATIENT 22:51
Error=xxxx
Device S/N=xxxxx
Call Help Desk

TEST ABORTED
 The error message will be displayed for 1 minute and then the WatchPAT™ device
will shut off.
 If this is a study with the tamper-proof bracelet and the wrong bracelet is connected
the "wrong bracelet" error message appears.
 If this is study with the tamper-proof bracelet and the bracelet is not connected the
"connect bracelet" error message appears in order to remind the patient to connect
the bracelet.
The following are the possible error/warning messages:
xxx1 - battery low

xx2x – uPAT probe error (used probe)
xx4x – File error (no new file)
xx8x - uPAT probe error (bad probe)
x4xx - SBP (Snore and Body Position sensor) missing warning
Note
The "x" stands for 0-F value (Hexadecimal code)

Error codes are additive, i.e. both uPAT probe and File errors will produce
error code xx6x.

3 PREPARATION FOR SLEEP STUDY
3.1 Charging the Battery

The battery must be charged every time the WatchPAT™ device is prepared for use. The
battery may be charged using the AC adapter provided.
To charge the WatchPAT™ device:

1. Gently slide the WatchPAT™ device out of the wrist strap until a click is
heard and the USB port is exposed.
2. Connect the USB port of the WatchPAT™ device to the AC adapter provided
(see Figure 6).
Warning
For charging use only an AC adapter having a 5V DC output, with 5W

minimum capacity. Using any other AC adapter may cause permanent
damage to the WatchPAT™ and may jeopardize the operator.
Figure 6 – Charging the WatchPAT™ Device
3. The LCD will blink slowly and the following screen will be displayed:
CHARGER 22:51
Bat=3.12 V
Charging…

 The display will show “CHARGER” if you are charging with the AC
adapter or “PC HOST” if you are charging with a computer.
 The current battery voltage is shown.
 Charge the battery the first time for approximately three hours.
Thereafter recharging takes approximately 1-1.5 hours.
4. When charging is complete, the LCD will stop blinking and the following
screen will be displayed:
CHARGER 22:51
Bat=4.2 V
Charging complete
5. Disconnect the AC adapter or communication cable. The WatchPAT™ device

will switch off in 30 seconds.
6. Reseat the WatchPAT™ device in the wrist strap by gently sliding it back in
until a click is heard.
Should a charging error arise the LCD will blink rapidly and the following screen will be
displayed.
CHARGER 22:51
Bat=4.2 V
Charger fault
3.2 Preparing the Snore and Body Position Sensor

Attach the small round double sided adhesive sticker to the Snore and Body Position sensor
on the back side (front side has a man image), by peeling off the cover on one side of the
sticker.
For more details see Appendix A: WP200U Integrated snoring + Body Positioning Sensor
Operating
3.3 Preparing the Wrist Strap

The wrist strap requires no special preparation other than ensuring its cleanliness. You may
clean it if needed. See section ‎6.1 for detailed cleaning instructions.

3.4 Mounting the WatchPAT™ on the Wrist Strap
To mount the WatchPAT™ device on the wrist strap:
Gently slide the WatchPAT™ device into the wrist strap until a click is heard
indicating that it is properly seated.
3.5 Replacing the uPAT Probe

Warning
The uPAT probe connector is very sensitive and therefore should

never be left exposed. Keep the connector connected to the probe at
all times, especially during cleaning. Replace the probe just before
performing the Device test.
Remove a used probe by pressing the small tab (clip) marked by the arrow in Figure 7, and
then, holding the connector’s slider, gently slide it away from the probe – do not pull the
slider off by pulling the cord, as it may damage the wiring. Properly dispose of used probes.
Figure 7 – Disconnecting the Figure 8 – Probe Disconnected

Probe
Connect a new probe by inserting the blue slider to the probe until the blue tab of the probe
clicks into its place.
Note
Take care when inserting the blue slider to insure proper seating in the
probe.

uPAT probe
Snore and Body

Position sensor
Figure 9 – WatchPAT™ Fully Prepared
3.6 Preparing the WatchPAT™ Device for a New Study

Refer to the zzzPAT Software Manual for preparation of the WP200U for a new study.
3.7 Testing the WatchPAT™ Device

Run the built-in self-diagnostic facility as described in Section ‎2.4 above.
The WatchPAT™ device is now ready for performance of a sleep study by the patient
(Figure 9).
3.8 WP200U Self-diagnostic Test Results and Trouble-shooting

Should any of the self-diagnostic tests fail or report error messages refer to the trouble-
shooting guide in Section ‎9.

3.9 Packing the Carrying Case
The following items must be placed inside the carrying case, in their respective
compartments (see Figure 1 – Packed Device):
 The WatchPAT™ device mounted in the Wrist strap with the uPAT probe
attached.
 Step-by-Step Reference Guide to the WatchPAT™ device.
 Body Position and Snore sensor (optional)
 Cable for bracelet (optional for patient identification)
 2 extra uPAT probes and AC adapter (optional for multi-night)
Note
Demonstrating the use of the WatchPAT™ device to the patient (and

accompanying individual if needed), is important for obtaining reliable
recordings and improving patient confidence.

4 OPTIONAL FUNCTIONS
4.1 Using the integrated Snore & Body Position Sensor

The integrated sensor consists internally of two sensors: a snore sensor and a body position
sensor.
A - Integrated sensor Sensor Attachment
The integrated sensor is powered by the WatchPAT™ device and does not require a
battery. It is automatically activated by the WatchPAT™ device when plugged into the
Snore & Body position port.
The snore sensor is an acoustic decibel detector. It uses a very sensitive microphone that
responds to snoring and other sounds in the audio range and converts them to a small
analog voltage that provides a clear, reliable indication of the presence of these sounds.
The body position sensor uses a 3-axis accelerometer that provides a signal directly
proportional to the patient's sleeping posture (supine, prone, right, left and sit).
See Appendix A: WP200U Integrated snoring + Body Positioning Sensor Operating .
4.2 Tamper-Proof Testing with WatchPAT™ Device

The WatchPAT™ device Tamper-Proof bracelet is an add-on accessory used to
authenticate the patient doing a sleep study and assure the study is recorded from the right
person.
The bracelet is a single use small plastic band designed to be worn around the wrist of the
hand. It contains an electronic circuit that signals to the WatchPAT™ device the integrity
of the bracelet and a unique identification. During the night the bracelet is connected to the
WatchPAT™ device using a small cable (see Figure 10).

Cable for bracelet
Bracelet
Figure 10 – WatchPAT™ Device with Tamper-Proof Bracelet
Before the device is given to the patient for home sleep study, the technician identifies the
patient and secures the bracelet to the patient’s wrist by a tamper-proof connector that
ensures the bracelet will not be removed without cutting the Bracelet.
Figure 11 – Bracelet on Patient's Hand
When preparing the WatchPAT™ device for a sleep study, the technician pairs the Tamper-
Proof Bracelet and the device and registers the bracelet's unique ID in the WatchPAT™
device (see Appendix B: Tamper-proof testing with WaTCHPAT™200U).
The patient can wear the Bracelet for several days, continuing normal day-to-day activity
until he is ready to record his sleep study. Before starting the recording, the patient will
need to connect the Bracelet, via the bracelet's cable 2 connectors, to the WatchPAT™
device. The device will not start without connection to the paired Bracelet.

Figure 12 – WatchPAT™ Device Figure 13 – WatchPAT™ Device
with Cable for Bracelet with Bracelet
Figure 14 – Bracelet and WatchPAT™ Device on a Patient’s Hand
During the recording the device will periodically check the Bracelet connectivity. The
recording will be stopped if the connection to the Bracelet will be lost for the time
exceeding a predefined limit.
After the recording is completed the patient can cut the Bracelet along the dotted line and
return it with the device for study analysis.
.
Figure 15 – Cut the Bracelet on a Specified Location

4.3 Multi-night study
A patient study may be defined as multi-night study and the patient can sleep up to 3 nights
with the same WatchPAT™ device. The multi-night option may be selected during New
Study function (see zzzPAT Operation Manual).
If a 3 night multi-night option is selected the patient must replace the uPAT probe and
charge the device between nights. Two extra uPAT probes and a WatchPAT™ device AC
adapter must be added to the WatchPAT™ device case.
If a 2 night multi-night option is selected the patient must replace the uPAT probe only
after the first night without the need to charge the device between nights. One extra uPAT
probe must be added to the WatchPAT™ device case.
In case of multi-night study all of the patient studies will be loaded automatically to the
zzzPAT during the upload (see zzzPAT Operation Manual).
Charger
2 extra probes
Figure 16 – Case for 3 Night Multi-night Study

5 DATA DOWNLOAD AND ANALYSIS
Following the sleep study the WatchPAT™ device is returned to the referring sleep clinic
for data downloading and analysis by the zzzPAT software.
To download and analyze the study data:

1. Connect the USB port of the WatchPAT™ device to the computer
(see Figure 4) The WatchPAT™ device will switch off and then
switch on in charging mode.
2. Activate the zzzPAT software to download and analyze the study data.
See the zzzPAT Software User Manual for detailed instructions.

6 MAINTENANCE
The WatchPAT™ device has been designed and manufactured to meet all safety
requirements applicable to medical equipment. To ensure maximum safety of operation, the
system should be used and maintained in strict compliance with the safety precautions,
warnings and operating instructions provided in this Manual.
The system contains no user-serviceable parts. It should be maintained and serviced only by
qualified service personnel, authorized by Itamar Medical Ltd.
Note
Please refer to the Service Manual or the support section of the Itamar
Medical web site for preventive maintenance recommendations.
6.1 Cleaning
The various components of the WatchPAT™ device have different cleaning requirements:
 The WatchPAT™ device
 The wrist strap
 The Snore & Body Position sensor
6.1.1 Cleaning the WatchPAT™ Device

There is no need to clean the unit during ordinary operation. Should it become necessary to
clean the WatchPAT™ device, proceed as follows:
Wipe parts with a clean, dry, lint-free cloth.
Clean casing with lint free cloth lightly moistened with 70% ethyl alcohol or isopropyl
alcohol (IPA).
Warning
Clean the WatchPAT™ device only with the uPAT probe attached.
6.1.2 Cleaning the Wrist Strap

You may clean the wrist strap with lint free cloth lightly moistened with
70% ethyl alcohol or isopropyl alcohol (IPA).
In order to disinfect the wrist strap by immersing into disinfecting liquid
follow the steps:
Remove WatchPAT™ device from wrist strap
Immerse wrist strap in 70% ethyl alcohol or isopropyl alcohol (IPA)

6.1.3 The uPAT Probe
The uPAT probe is designed for a single use only. It may not be cleaned and
must be discarded and replaced before each study.
6.1.4 The Snore & Body Position Sensor

Using 70% ethyl alcohol, thoroughly clean both sensor and cable.
6.2 Handling
Handle with care:
 Use only the designated case for transportation
 Store at room temperature, and avoid direct sun light
 Do not expose the WatchPAT™ device to extreme temperature or
humidity conditions (such as storing in a car or bathroom)
Note
6.3 Replacing the uPAT Probe Cable
To replace the uPAT probe cable:
1. Carefully disconnect the uPAT probe cable from the WatchPAT™

device. Make sure you remove the screw prior to disconnecting the
uPAT cable.
Figure 17 – uPAT Probe Cable with Screw
2. Connect a new uPAT probe cable by gently inserting the connector

into the WatchPAT™ device. Make sure you secure back the screw.

Figure 18 – Replacing the uPAT Probe
Warning
Use only the original screw that belongs to the WatchPAT™ device.
Using different screw could harm the device.
Note
6.4 Replacing the Battery

Warning
Replace the battery only with an authorized battery provided by Itamar

Medical Ltd.
In the event of a battery error message during the self-diagnostic tests or after charging, it
may be necessary to replace the battery.
To replace the battery:
1. Open the battery compartment cover with a Phillips screwdriver.
2. Gently open the battery connector by disconnecting the 2 parts (you will need to
remove the transparent tape that secures the battery connector closed).
3. Remove the battery.
4. Insert the new battery into the battery compartment.
5. Insert the 3 pin connector into the corresponding battery connector (one pin is
longer so it may properly be inserted in only one direction). Secure the battery
connector closed with a small piece of transparent tape.
6. Close the battery compartment cover and secure back the screw.
Battery compartment cover
Phillips screw
Battery
Battery Connector -
Closed
3 pin Connector
Figure 19 – Replacing the Battery
Note
6.5 Setting the Time and Date of the WatchPAT™ device

The WatchPAT™ device Time and Date can be set through the zzzPAT application. Refer
to the zzzPAT Software Manual for preparation of the WatchPAT™ device for a new
study.
6.6 Storing the WatchPAT™ device
 The WatchPAT™ device should be stored in its carrying case at room temperature
and low humidity.
 In order to preserve battery performance when the WatchPAT™ device is not in
use, store with the battery fully discharged.
 Before storing the WatchPAT™ device allow it to deplete the battery charge until it
shuts down automatically.

7 APPLYING THE WATCHPAT™ DEVICE
Note
These instructions are designed to help the patient use the WP200U after
seeing a demonstration by trained personnel of how to mount the probes
on his/her fingers and correctly operate the WatchPAT™ device .
The following detailed instructions are summarized in the patient’s step-by-step reference
guide. They are written as if the reader is the patient using the WatchPAT™ device.
7.1 Preparing for Use of the WatchPAT™ Device

Before using the WP200U, review the following notes:
 Remove tight clothing, rings, watches and jewelry from your non-dominant hand
and wrist and from your neck and chest.
 We recommend that the uPAT probe be attached to the index finger of your non-
dominant hand (Figure 20). The following instructions relate specifically to this
finger. Patients with very large fingers may use their small finger (pinky) for the
uPAT Probe.
 Ensure that fingernail of finger that will be monitored are well trimmed, (less than
1mm from nail bed) with no jagged edges. Clip and file nail, if necessary.
 Remove artificial fingernail or dark nail polish from the monitored finger.
 You may need some assistance putting on the WatchPAT™ device. If needed have
someone present to assist you.
 Make sure the room you are sleeping in is as quiet as possible during the night, turn
off any possible noise sources. When using the Snore & Body Position sensor it is
advised to sleep alone in the room.

Index finger
Small (pinky) finger
Figure 20 – Finger Designation
7.2 Applying the WatchPAT™ Device

To apply the WatchPAT™ device to your wrist:

1. Open the carrying case and take out the wrist strap with the WatchPAT™ device
mounted. All parts should already be connected, as illustrated in Figure 9.
2. Ensure that the WatchPAT™ device is firmly seated in the wrist strap. If not, gently
seat the WatchPAT™ device in the strap by sliding it into its seating position. You
will hear a click when the WatchPAT™ device is properly seated in the strap.
3. Place the wrist strap with the WatchPAT™ device on the non-dominant arm and
close it snugly but not tightly. Ensure that the rounded end is towards the body and
the open end towards the fingers. You may find it convenient to place the wrist strap
with the WatchPAT™ device face down on the table and then place the back of the
wrist over the wrist strap in order to fasten the straps (Figure 21).
4. At this point the uPAT probe is hanging loose (Figure 22Figure 22 – Wearing the
WatchPAT™ Device).
Figure 21 – Putting On The Wrist Strap Figure 22 – Wearing the WatchPAT™ Device
7.3 Attaching the uPAT Probe

Proper probe placement is critical for good performance.
Note
The tab inside the probe should be removed only AFTER the finger is
inserted into the probe.
To attach the uPAT probe:

1. Insert your index finger (or other if so instructed) gently into the probe until
it reaches the end (see Figure 23 – ).
2. Make sure that the paper tab marked TOP is above your nail.
3. Detach and gradually remove the tab marked TOP slowly and firmly while
pressing the tip of probe against a hard surface (WatchPAT™ case, table,

etc.) until the tab is completely removed from the probe (Figure 24). You
might feel a slight suction once the tab is removed.
The uPAT probe is now attached (Figure 25).
Figure 23 – Placing Finger In uPAT Probe
Figure 24 – Removing TOP Tab
Figure 25 – Wearing the WP200U – Ready for Sleep
Note
DO NOT remove the uPAT probe before the night study is terminated.
Once the probe is removed it cannot be re-attached.

Note
If the Snore & Body position sensor is included in the WatchPAT™

device case see Appendix A: WP200U Integrated snoring + Body
Positioning Sensor Operating Instructions
7.4 Switching On the WatchPAT™ device

You are now ready to switch on the WatchPAT™ device.
Just before you lie down to go to sleep, firmly press the ON/Enter center button (Figure 3)
until the LCD display lights up. After a short delay the LCD will display “Good Night!
Recording…”
PATIENT 22:51
GOOD NIGHT!!!
Time elapsed=9:50
Recording…
Note
To conserve the battery the LCD display will switch off after a few
seconds. Pressing any button will restore the display for about 30
seconds.
7.5 When You Wake Up

When you awake, remove the WatchPAT™ device from your arm as follows:
1. Remove both probes from your fingers.
2. Take off the wrist strap.
3. Place all parts in the carrying case.
Note
Pressing the center button does not switch off the WatchPAT™ device.
Approximately ten hours after the WatchPAT™ device is turned on, it
will switch off. This is normal.

7.6 Important Notes
Wearing the WatchPAT™ device should not cause any discomfort or pain. If you
experience wrist or arm discomfort, loosen up the wrist strap. If the discomfort is not
alleviated immediately, call the service number.
 Do not attempt to connect or disconnect any part of the unit.
 Do not try to introduce any foreign object into the unit.
 Do not try to connect the unit to an electrical supply or any other unit,
machine or computer.
 If any part appears disconnected or does not resemble the illustrations, call
the service number for assistance.
 Do not, under any circumstances, attempt to fix the problem yourself.
If you have any questions about using the machine, before, during or after your at-home
recording session, call the service number.

8 PATIENT TRAINING – GUIDELINES
Instruct the patients (and accompanying individual if needed) how to attach
and use the WP200U prior to use.
8.1 Walk Through the Process of Using the WatchPAT™ device

 Product introduction – WatchPAT™ device, wrist strap, uPAT probe
 WatchPAT™ device and wrist strap attachment
 Probe and sensor attachment
 Switch on
 Ending the study
8.2 Product Introduction

 Open the Demo-case and introduce the ‘Quick guide step-by-step’
instruction manual.
 Introduce each component by its name and identify it as in the figures in the
manual.
8.3 Applying the WatchPAT™ device

Use the Demo Kit.
 Demonstrate how to apply the WatchPAT™ device on your wrist while
following the ‘step by step’ guidelines and referring to the relevant figures.
 Demonstrate the following:
1. Hand Preparation
 Remove rings, watches and jewelry from hand
 Remove fingernail polish and artificial nails
 Make sure index finger nail is closely trimmed
2. Attaching the Snore & Body Position Sensor (optional)
 The sensor is attached to the patient’s chest right under
the sternal notch. The sternal notch is the little U shape
where the collar bones meet at the top of the breast bone.
 Attach the round double sided adhesive sticker to the
blue side of the sensor. To position the sensor attach it
with the man image standing up, after peeling off the
round adhesive sticker and pressing against the skin.
 Make sure the sensor is tight against the skin.
 Secure the snoring sensor in place with medical tape.

3. Wearing the Wrist Strap
 Should be comfortable, not too tight.
4. Attaching the WatchPAT™ Device
 Make sure the WatchPAT™ device is properly mounted
on the wrist strap. If it is loose, gently slide it in until you
hear a click.
5. Attaching the uPAT Probe
 Insert finger all of the way into the probe
 Press tip of probe against a hard surface (WatchPAT™
device case, table, etc.) while removing tabs in order to
keep the finger from moving inside the probe
 Remove the Tab by pulling slowly and gradually
 The probe is limited to a SINGLE USE. Do not remove
probe during the night.
8.4 Switching on the WatchPAT™ Device

 Demonstrate switching on the WatchPAT™ device by pressing the round
center button
 Push button firmly until the LCD display lights up
8.5 Removing the WatchPAT™ Device

 Demonstrate how to remove the WatchPAT™ device and place it back in
the carrying case.
 The WatchPAT™ device doesn’t switch off – once turned on it will record
until the battery is exhausted.
8.6 Patient Training

 Following your demonstration have the patient attach the demo device by
himself or with the assistance of accompanying individual if needed.
 Verify that the attachment is properly done.
8.7 Review Safety, General and Functional Issues

 Avoid exposing the WatchPAT™ device to extreme conditions (high
temperature, high humidity)
 Provide a telephone number to call in case of questions or problems.

9 TROUBLESHOOTING GUIDE
9.1 Operator Error Messages

If an error message is displayed while performing the self-diagnostic tests, take the actions
specified below. If the problem persists contact Itamar or an authorized representative.
Table 1 – Operator Troubleshooting

Error Possible Reason Action
File error
Not loaded Study not initialized for new Connect device to PC and perform New
patient Study in zzzPAT
Battery error % full Battery defective or Charge battery or replace
uncharged
Probe error
Used Probe previously used Replace probe
Missing Probe absent Attach probe
Bad Probe is defective Replace probe
Hardware status error code WatchPAT™ device Consult Itamar or authorized representative
defective
SBP disconnected even if it WatchPAT™ device or Consult Itamar or authorized representative
is connected SBP sensor defective
RTC faulty WatchPAT™ device Consult Itamar or authorized representative
defective
Short recording time Patient removed the WP200U Explain proper use to patient
or probe from hand
prematurely
Insufficient battery charge Recharge battery and try again
caused early termination of
recording
Damaged WatchPAT™ Contact your authorized sales representative
device

9.2 Patient Error Messages
If an error message is displayed when the patient powers on the WatchPAT™ device, the
patient should take the actions specified below. If the problem persists the patient may
contact Itamar or an authorized representative directly.
Table 2 – Patient Troubleshooting

Error Possible Reason Action
WatchPAT™ device ON button not activated Press the ON button firmly for at least 3
doesn’t switch on seconds
uPAT probe not connected Ensure probe is connected and try again
Probe disconnected Probe may not be connected, Check connection of probe to cable and cable to
or may be a used probe the WatchPAT™ device; check if probe has
been previously used and replace with new
probe if necessary
Hardware code WatchPAT™ device Contact Itamar or authorized representative
failure

10 SPECIFICATIONS
Table 3 – WatchPAT™200U Specifications
Properties Description
uPAT Probe Itamar’s proprietary probe. Measures PAT and
Oximetry.
Recording Time 10 hours (minimum)
Channels Measuring 6 signals: PAT, Pulse rate, Oximetry,

Actigraphy, Snoring (optional), Body Position
(optional)
Sample Resolution PAT and Actigraph – 12 bit; oximetry – 1%
Snoring – 12 bit, Body Position – 5 discrete states
User Interface LCD display
Oximetry Arms ≤ 3% (in range 70%-100%)
Accuracy Pulse rate 30-150 ± 1 bpm

Amplitude 0-0.5V ± 10%
PAT Channel Bandwidth 0.1-10 Hz
Data Storage Media Micro SD card
Capacity 64 MB (minimum)
Format type Formatted to FAT 32
Power Supply Battery Proprietary, rechargeable Lithium Ion Battery

Capacity > 500-700 mAh
Cell Type Lithium Ion cell type

Internal Charger Proprietary Lithium Ion battery charger
External Power Supply 5V DC, 5W with USB connector
Operating Voltage 3.3 V
Temperature Operation 00C to 40 0C
Storage (Device) -200C to 40 0C
Transport (Device) -200C to 60 0C
Storage & Transport 00C to 40 0C
(Probe)
Humidity Operating 10% – 93% (non-condensing)
Storage & Transport 0% – 93% (non-condensing)

Atmospheric Operating & Storage 10 – 15 psi
pressure
Transport 8 – 15 psi
Dimensions LxWxH 80 x 50 x 20 mm
Weight 130 gr (excluding uPAT probe weight of 20 gr)

APPENDIX A: WP200U Integrated snoring + Body Positioning Sensor
Operating Instructions
Must be used with zzzPAT v 4.3 and above and WatchPAT™200
Thank you for purchasing an Integrated Snore & Body Position Sensor.
Description
The integrated sensor consists internally of two sensors: a snore sensor and a body position
sensor.
A B
A
A - Integrated sensor A - Sensor attachment

B - Sternal notch
The integrated sensor is powered by the WatchPAT™ device and does not require a
battery. It is automatically activated by the WatchPAT™ when plugged into the Snore &
Body position port.
The snore sensor is an acoustic decibel detector. It uses a very sensitive microphone that
responds to snoring and other sounds in the audio range and converts them to a small
analog voltage that provides a clear, reliable indication of the presence of these sounds.
The body position sensor uses a 3-axis accelerometer that provides a signal directly
proportional to the patient's sleeping posture (supine, prone, right, left and sit).
Indications of use
The integrated Snoring & Body position sensor is an accessory of the WatchPAT™ home
care device for use with patients suspected to have sleep related breathing disorders. The
integrated sensor monitors the snoring level, which aids in the evaluation of the severity of
sleep related breathing disorders, and the body position which aids in the evaluation of the
type of sleep related breathing disorders.
Preparing the sensor

 Attach the round double sided adhesive sticker to the blue side of the sensor.

Applying the sensor
Make sure the room you are sleeping in is as quiet as possible during the night, turn off any
possible noise sources. When using the SBP it is advised to sleep alone in the room.
 The sensor is attached on the patient’s chest right under the sternal notch. The sternal
notch is the little U shape where the collar bones meet at the top of the breast bone.
 To position the sensor attach it with the man image standing up, after peeling off the
round adhesive sticker and pressing against the skin.
 Make sure the sensor is tight against the skin.
 Secure the sensor in place with medical tape.
Cleaning the sensor

Using 70% ethyl alcohol, thoroughly clean both sensor and cable.
SPECIFICATIONS
Snoring Sensor Technology Sensitive microphone
Body Position Sensor 3-axis Accelerometer
Technology
Signal Amplitude 0-3.3 V
Connector Type 1 mm medical safety connector plug from Plastics1
Wire Length: 3.2 foot (100 cm)
Physical Size 1.3 inch diameter (32 mm diameter)
Weight 12 gr
Warranty 6 months
Temperature Operation 0 to 40 0C
Storage -20 to 40 0C
Transport -20 to 60 0C
Humidity Operating, Storage & 0% – 93% (non-
Transport condensing)
Atmospheric pressure Operating, & Storage 10 – 15 psi
Transport 8 – 15 psi

Snoring and Body Position Accuracy
This section gives statistical performance measure for Itamar SBP sensor, when used with
the WatchPAT™ device.
I. Body Position
The body position measured by the WatchPAT™ device with Itamar SBP sensor was
compared to the gold standard, manual scoring of the video recording of 31 patients, in 1
minute’s epochs (total of 7111 epochs) during sleep.
The Agreement between the device and the video recording was 90%.
Simple Kappa agreement value was 0.8185 (95% confidence level of 0.8059 and 0.8311).
II. Snoring
The snoring level measured by the WatchPAT™ device with Itamar SBP sensor was
compared to a gold standard PSG dB-meter placed 1 meter from patient’s head. The study
included 26 patients, and the analysis was done in 30sec epochs.
The correlation coefficient was calculated using Pearson method, assuming a linear relation
between the results of the two devices. A statistically significant correlation was calculated
between the two devices: r=0.65 p value<0.0001.
The next figure shows a scatter plot of sleep disturbance Index produced by WatchPAT™
device and dB-meter, with linear regression line.
An estimation of the error in each snoring level was calculated by looking at the
WatchPAT™ device measurement cut by the results of dB-meter in intervals of 1 dB in the
range of above 40dB (below 40 dB was considered not clinically significant being
background noise). A high correlation was observed between the results of the two devices
for the range of 40-70dB (where sufficient data points were gathered), meaning the
resemblance in the results uniformly existed for all the snore levels measured.
The next table presents the statistics of WatchPAT™ device measurements per dB-meter
calculation at that range.

PSG Coef. Of Lower Upper
DB N Mean Std Variation Min Max Median 95% 95%
Value [%] CI CI
40 2033 41.10 1.89 4.60 40 54 40 41.01 41.18
41 1319 41.61 2.67 6.43 40 54 41 41.47 41.76
42 908 42.68 3.79 8.88 40 62 41 42.44 42.93
43 746 44.12 4.49 10.19 40 58 42 43.80 44.44
44 719 44.75 4.65 10.39 40 65 43 44.41 45.09
45 643 45.90 5.07 11.04 40 59 45 45.51 46.30
46 602 46.45 5.17 11.13 40 59 46 46.04 46.86
47 590 47.39 5.31 11.21 40 66 47 46.96 47.82
48 568 48.03 5.17 10.76 40 61 49 47.60 48.45
49 414 48.56 5.33 10.97 40 64 49 48.05 49.08
50 369 49.07 5.27 10.75 40 61 49 48.53 49.60
51 334 49.68 5.66 11.39 40 63 50 49.07 50.28
52 335 50.00 5.58 11.17 40 64 51 49.39 50.59
53 311 51.18 5.56 10.86 40 63 51 50.56 51.79
54 253 51.71 5.78 11.19 40 66 52 51.00 52.42
55 209 51.85 5.49 10.59 40 66 52 51.11 52.60
56 182 51.91 5.62 10.82 40 64 52 51.09 52.72
57 129 52.29 5.91 11.30 41 64 52 51.26 53.32
58 95 54.94 5.94 10.82 42 67 55 53.73 56.15
59 66 55.53 6.37 11.47 42 66 55.5 53.97 57.10
60 72 57.82 5.92 10.24 44 66 58 56.43 59.21
61 58 58.48 6.31 10.78 43 68 58.5 56.82 60.14
62 43 59.47 6.56 11.02 46 68 60 57.45 61.48
63 32 59.63 4.15 6.96 50 67 59 58.13 61.12
64 15 62.53 3.93 6.28 56 68 64 60.36 64.71
65 22 64.41 6.21 9.64 49 70 67 61.66 67.16
66 48 66.90 3.66 5.48 59 70 68.5 65.83 67.96
67 42 65.76 3.28 4.99 60 71 67 64.74 66.78
68 27 64.56 2.67 4.13 55 68 65 63.50 65.61
69 6 67 2.37 3.53 64 70 67 64.52 69.48
The results are also presented in the next figure. The figure presents the mean WatchPAT™
device with SD error bar.

Summary statistics (mean ± SD) of WatchPAT™200U device by dB-meter levels

APPENDIX B: TAMPER-PROOF TESTING WITH WATCHPAT™200U
t Action Comment
Important This short guide is designed to instruct a Make sure the zzzPAT version is:
Notes trained operator of the WatchPAT™ 4.2.58 or higher
Important Notes
device how to perform a Tamper-Proof Make sure the WatchPAT™ device

Testing with the bracelet & the embedded software version is:
WatchPAT™ device. For complete 2.2176 or higher
WatchPAT™ training & instructions Make sure you enabled the
please refer to the WatchPAT™ device “Tamper-Proof Testing” option
user manual and to the zzzPAT user from the zzzPAT “Setup” menu 
manual. “General Settings”
1. Preparing a While preparing the new study on the

New Study on zzzPAT (refer to the user manual for
Study Preparation
zzzPAT detailed instructions), check the box

“Study with Tamper-Proof Testing” at
the bottom of the “New Study” screen.
Note: Once you enable this option you

will HAVE to use a bracelet for the
night study. The WatchPAT™ device
will NOT function without a bracelet
connected to it.
2. Bracelet Select a Tamper-Proof Bracelet for the
study.
Bracelet Preparation
3. Connecting the Connect the gray cable with the red and
Cable to the white connectors to the WatchPAT™
WatchPAT™ device socket.
device

t Action Comment
4. Connecting the Connect the red and white connectors

Bracelet
(other side of the gray cable) to the red
and white snaps on the bracelet
respectively.
5. Pairing the Perform the regular site diagnostic test

Bracelet Preparation
WP200U (“device test” as described in the user

device and the manual).
Bracelet: Make sure the bracelet is connected
Site-Diagnostic before starting the test.
Test After tests passed successfully,
disconnect the bracelet from the
WatchPAT™ device and store them
together.
Note: Once the device testing has been

done with the bracelet connected – the
SPECIFIC bracelet must be used with
the specific WP200U. NO OTHER
BRACELET WILL WORK WITH
THIS WatchPAT™ device. (A unique
ID of this bracelet is registered in the
WatchPAT™ device.)

t Action Comment
1 Placing the Make sure you have all 3 parts: the 1

Bracelet on the bracelet and two white plastic parts.
Subject Place the bracelet upside down on a flat
surface (white side facing up).
Insert the white plastic part into the two
separated holes (flat side facing up).
Wrap the bracelet around the wrist of the

non-dominant arm (tested arm) of the
subject.
2
Insert the white plastic parts into the 2
holes. Make sure it is snug but not too
tight.
Subject Setup
If there is some loose strap left, fold it

and re-insert it into the holes.
DO NOT CUT LOOSE STRAP –
CUTTING IT WILL RENDER 3
3 BRACELET UNUSABLE
Secure the bracelet by placing the

second white plastic part on-top of the
first.
4 Make sure it is secured tightly. 4

t Action Comment
6. Explain to The subject may choose to perform the

Subject night study during any night during the
next week.
It’s OK to shower with the bracelet.
Instruct subject to turn on the

WatchPAT™ device only after it is
connected to the bracelet.
Explain to Subject
THE BRACELET IS NOT TO BE

REMOVED UNTIL THE NIGHT
STUDY IS COMPLETED. Removing
the bracelet before or during the night
will cause the device to shut down.
In the morning, instruct to cut the

bracelet along the dotted line, using
small scissors and to put it in the
WatchPAT™ device case along with all
the other parts (DO NOT THROW
BRACELET AWAY).
Do not try to connect ANY other device

to the bracelet.

APPENDIX C: LICENSE AGREEMENT
License To Operator From Itamar

IMPORTANT – PLEASE READ THIS LICENSE AGREEMENT CAREFULLY
BEFORE INSTALLING OR OTHERWISE USING THE LICENSED SOFTWARE (AS
DEFINED BELOW) OR THE PRODUCT WITH WHICH YOU RECEIVED THIS
LICENSE AGREEMENT. THIS LICENSE AGREEMENT APPLIES TO (a) ALL
LICENSED SOFTWARE, (b) ALL LICENSED PRODUCTS (AS DEFINED BELOW),
AND (c) ALL THIRD PARTY PRODUCTS INTO WHICH A LICENSED PRODUCT
OR LICENSED SOFTWARE IS INCORPORATED. SHOULD YOU HAVE ANY
QUESTIONS CONCERNING THIS LICENSE AGREEMENT, PLEASE CONTACT
THE VENDOR FROM WHICH YOU PURCHASED THE LICENSED SOFTWARE,
LICENSED PRODUCT, OR PRODUCT INTO WHICH A LICENSED PRODUCT OR
LICENSED SOFTWARE IS INCORPORATED. YOU MAY ALSO CONTACT
ITAMAR AT THE ADDRESS PROVIDED AT THE END OF THIS LICENSE
AGREEMENT.
This License Agreement is a legal agreement between you (as an individual, company,
organization or other entity) and Itamar Medical Ltd. (“Itamar”). By installing, copying, or
otherwise using the Licensed Software, and/or by using the Licensed Product or third party
product into which a Licensed Product or Licensed Software is incorporated (“Third Party
Product”), you agree to be bound by the terms of this License Agreement with respect to
the Licensed Software and Licensed Products. If you do not agree to the terms of this
License Agreement, including, without limitation, the Restrictions on Use as provided in
Section 2 do not install, use or copy the Licensed Software or use the Licensed Product or
the Third Party Product.
The Licensed Software and the Licensed Products are protected by US patent laws, trade
secret laws, copyright laws, and international treaty provisions as well as other intellectual
property laws and treaties. Therefore, you must treat the Licensed Software and the
Licensed Products like any other copyrighted and protected material or product. All title to
the Licensed Software and all intellectual property rights in and to the Licensed Software
and the Licensed Products shall remain with Itamar.
1. DEFINITIONS
1.1. “Licensed Product(s)” means the Watch_PAT200 (Watch-PAT200), the
Site_PAT200, the uPAT Probe and the corresponding components of any
Third Party Product with which this License Agreement was received.
Some Licensed Products are stand-alone products and some Licensed
Products are incorporated as components within Third Party Products, in
each case sold or otherwise made available, by Itamar and/or third
parties. If you have received this License Agreement with a Third Party
Product, this License Agreement applies only to the Licensed Product
incorporated as a component within such Third Party Product.
1.2. “Licensed Software” means the zzzPAT software, the associated media
and accompanying materials provided to you with such zzzPAT software.
Some Licensed Software is a stand-alone product and some Licensed
Software is incorporated as a component within a Licensed Product, in
each case sold or otherwise made available, by Itamar and/or third
parties. If you have received this License Agreement with a Licensed
Product which incorporates the Licensed Software as a component within
such Licensed Product, this License Agreement applies to the Licensed
Software.
2. GRANT OF LICENSE AND RESTRICTIONS ON USE

2.1 Itamar hereby grants you a non-exclusive right to use the Licensed Software , solely
for its intended use in sleep medicine (with the term "sleep medicine" including
Cheyne-Stokes respiration as well as research in sleep medicine and Cheyne-Stokes
respiration) (i) with the Licensed Product(s) and (ii) in accordance with the provisions
of this License Agreement and the instructions provided in the documentation
accompanying the Licensed Software and the Licensed Product You may make one
copy of the Licensed Software solely for backup or archival purposes, or transfer the
Licensed Software to a single hard disk, provided you keep the original solely for
backup or archival purposes. However, you may not cause any Licensed Software
which is not designed for use on a server, to execute or be loaded into the active
memory or media of more than one computer at any one time.
2.2 Any use of the Licensed Software and/or Licensed Product other than as set forth in
Section 2.1 above is strictly forbidden. Without derogating from the generality of the
above, you may not:
 distribute, reproduce, copy, assign, rent, lease, or otherwise transfer the rights
granted to you under this License Agreement to any third party except explicitly as
set forth in this License Agreement;
 reverse engineer, decompile, or disassemble, as applicable, the Licensed Software
or the Licensed Product, except as expressly permitted by applicable law; or
 modify in any manner the Licensed Software and/or the Licensed Product unless
obtaining the prior written consent of Itamar.
3. TRADEMARKS
Cardio-PAT™, Sleep-PAT™ and all trademarks and logos, which appear on or in
connection with the Licensed Software and/or the Licensed Products, as may be amended
from time to time, are, unless stated otherwise, trademarks of Itamar. No right, license, or
interest to such trademarks are generated or granted hereunder other than the limited right
to use provided herein, and you agree that no such right, license, or interest shall be
asserted by you with respect to such trademarks. You may not remove or destroy any

copyright, trademark, logo or other proprietary marking or legend placed on or contained in
the Licensed Software or a Licensed Product.
4. LIMITED WARRANTIES AND DISCLAIMERS

a. Against Infringement. Itamar hereby warrants to you that it has the right to grant you
the license to use the Licensed Software and/or the Licensed Product and to enter into this
License Agreement and that neither the Licensed Software nor the Licensed Product(s)
infringes the intellectual property rights of any third party.
b. As to Licensed Product. Itamar warrants that the Licensed Product with which this
License Agreement was delivered, will be free from defects in design, materials and
workmanship for a period of one year from the date of delivery of the Licensed Product to
you. If the Licensed Product contains a defect in design, materials or workmanship and
such Licensed Product is returned to Itamar within one (1) year of delivery of the Licensed
Product to you, Itamar will repair or replace the Licensed Product, or issue a credit for the
purchase price of the Licensed Product, with the choice to repair, replace or credit being
within the sole discretion of Itamar. The foregoing repair, replacement or credit remedy
will be your sole remedy for breach of the warranty set forth in this Section 4(b).
c. As to Licensed Software. Itamar warrants that for a period of ninety (90) days from the
date of delivery of the Licensed Software to you, the Licensed Software will, under normal
use, be free from defects in materials and workmanship and will perform substantially as it
is intended to perform. If during such ninety (90) day period, the Licensed Software has a
defect in materials or workmanship or does not perform substantially as it is intended to
perform, Itamar shall (a) attempt to correct or assist you around errors with efforts which
Itamar believes suitable to the problem, (b) replace the Licensed Software with a
functionally equivalent software, or (c) issue a credit for the purchase price of the Licensed
Software, with the choice to correct or assist, replace or credit being within the sole
discretion of Itamar. The foregoing correct or assist, replacement or credit remedy will be
your sole remedy for breach of the warranty set forth in this Section 4(c).
d. Limitation of Warranties. The warranties contained in Sections 4(b) and 4(c) above do
not cover damage to the Licensed Products or the Licensed Software caused by accident,
misuse, abuse, negligence, failure to install in accordance with Itamar’s installation
instructions, failure to operate under conditions of normal use and in accordance with the
terms of the documentation accompanying the Licensed Product and/or the Licensed
Software, failure to maintain in accordance with applicable documentation accompanying
the Licensed Product and/or the Licensed Software, alteration or any defects not related to
materials or workmanship, or in the case of Licensed Products, design, materials or
workmanship. This warranty does not cover damage which may occur in shipment. This
warranty does not apply to Licensed Products and/or Licensed Software not purchased new.
This warranty does not apply to any Licensed Product or any individual parts of a Licensed
Product which have been repaired or altered by anyone other than Itamar or a person or
entity authorized by Itamar to repair Licensed Products.

While every reasonable effort has been made to ensure that you will receive Licensed
Software that you can use, Itamar does not warrant that the functions of the Licensed
Software will meet your requirements or that the operation of the Licensed Software will be
uninterrupted or error free. Itamar is not responsible for problems caused by changes in the
operating characteristics of the hardware or operating system software you are using, nor
for any problems in the interaction of the Licensed Software with non-Itamar software.
ITAMAR HEREBY DISCLAIMS, WITH RESPECT TO THE LICENSED PRODUCTS

AND THE LICENSED SOFTWARE, ALL OTHER WARRANTIES AND
CONDITIONS, WHETHER EXPRESS OR IMPLIED, INCLUDING, BUT NOT
LIMITED TO, ANY WARRANTIES OR CONDITIONS OF OR RELATED TO
MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, ACCURACY OR
COMPLETENESS OF INFORMATION, LACK OF NEGLIGENCE AND
CORRESPONDENCE TO DESCRIPTION.
5. LIMITATION OF LIABILITY
(A) TO THE MAXIMUM EXTENT PERMITTED BY APPLICABLE LAW, EXCEPT
FOR DAMAGES ARISING UNDER SECTION 4(A) ABOVE, IN NO EVENT SHALL
ITAMAR BE LIABLE TO YOU FOR DAMAGES IN EXCESS OF THE PURCHASE
PRICE YOU PAID FOR THE LICENSED SOFTWARE, THE LICENSED PRODUCT
OR THE APPLICABLE THIRD PARTY PRODUCT. THE FOREGOING LIMITATION
SHALL BE APPLICABLE REGARDLESS OF WHETHER THE ACTION GIVING
RISE TO SUCH DAMAGES IS IN TORT, CONTRACT, STRICT PRODUCTS
LIABILITY, OR OTHERWISE.
(B) IN NO EVENT SHALL ITAMAR BE LIABLE FOR ANY SPECIAL,

INCIDENTAL, INDIRECT OR CONSEQUENTIAL DAMAGES WHATSOEVER
ARISING OUT OF OR IN ANY WAY RELATED TO THE USE OF OR INABILITY TO
USE THE LICENSED SOFTWARE AND/OR THE LICENSED PRODUCT AND/OR
THE THIRD PARTY PRODUCT, OR THE PROVISION OF OR FAILURE TO
PROVIDE SUPPORT SERVICES BY ITAMAR, EVEN IF ITAMAR HAS BEEN
ADVISED OF THE POSSIBILITY OF SUCH CONSEQUENTIAL DAMAGES. THE
FOREGOING DISCLAIMER OF CONSEQUENTIAL DAMAGES SHALL BE
APPLICABLE REGARDLESS OF WHETHER THE ACTION GIVING RISE TO SUCH
DAMAGES IS IN TORT, CONTRACT, STRICT PRODUCTS LIABILITY, OR
OTHERWISE.
(C) IN ORDER TO BE ENTITLED TO INDEMNIFICATION HEREUNDER IN

CONNECTION WITH AN INFRINGEMENT CLAIM, YOU MUST (i) NOTIFY
ITAMAR IN WRITING PROMPTLY UPON BECOMING AWARE OF AN
INFRINGEMENT CLAIM OR THE POSSIBILITY THEREOF, (ii) GRANT ITAMAR
SOLE CONTROL OF THE SETTLEMENT, COMPROMISE, NEGOTIATION AND
DEFENSE OF ANY SUCH ACTION, AND (iii) PROVIDE ITAMAR WITH ALL
INFORMATION RELATED TO THE ACTION THAT IS REASONABLY REQUESTED
BY ITAMAR. NOTWITHSTANDING THE FOREGOING, ITAMAR SHALL HAVE
NO INDEMNIFICATION OBLIGATIONS WITH RESPECT TO ANY INFRINGEMENT
CLAIM TO THE EXTENT ARISING FROM YOUR USE OF THE LICENSED
PRODUCT AND/OR LICENSED SOFTWARE IN CONJUNCTION WITH OTHER
HARDWARE OR SOFTWARE WHERE USE WITH SUCH OTHER HARDWARE OR
SOFTWARE GAVE RISE TO THE INFRINGEMENT CLAIM.
6. TERMINATION
Without prejudice to any other rights or remedies, Itamar may terminate this License
Agreement immediately if you fail to comply with any of its terms and conditions. In the
event of such termination, you must, within ten (10) business days of receiving notice of
termination from Itamar, cease all use of the Licensed Software and destroy all copies
thereof, and cease all use of the Licensed Product (including Licensed Product incorporated
within Third Party Product).
7. TRANSFERABILITY
You may only transfer or assign the rights and obligations hereunder together with the
Licensed Software and/or the Licensed Product or Third Party Product as a whole, without
retaining any rights or, subject to Sections 2 and 3 above, any obligations arising after the
date of such transfer or assignment, or retaining any installed or uninstalled copy of the
Licensed Software, the Licensed Product or the Third Party Product. Any attempt by you to
rent, lease, sublicense, assign or transfer any of the rights, duties or obligations hereunder in
any other way is forbidden and shall be null and void.
8. SEVERABILITY
Should any term or provision of this License Agreement be declared void or unenforceable
by any court of competent jurisdiction in any country or countries, such declaration shall
have no effect on the remainder of this License Agreement in such country or countries, or
on this License Agreement in other countries.
9. NO WAIVER
The failure of either party to enforce any rights granted to it hereunder or to take action
against the other party in the event of any breach hereunder shall not be deemed a waiver
by that party as to subsequent enforcement actions in the event of future breaches.
10. GOVERNING LAW AND JURISDICTION

This License Agreement is governed by the laws of the State of New York, excluding its
conflict of laws principles. The United Nations Convention on Contracts for the
International Sale of Goods shall not apply to any of the transactions contemplated by this
License Agreement.
11. ENTIRE UNDERSTANDING

This License Agreement represents the complete and exclusive understanding between you
and Itamar concerning the license by Itamar to you of Licensed Software and Licensed
Products and supersedes all prior agreements and representations between the parties with
respect to the subject matter hereof, unless specifically stated otherwise in a writing signed
by Itamar and you. This License Agreement may not be amended other than by a written
agreement specifically intended for this purpose and signed by Itamar and you.
Note: Should you have any questions concerning this License Agreement, or if you desire
to contact Itamar for any reason, please write to: Itamar Medical Ltd., 9 Halamish St.,
Caesarea Ind. Park, 3088900, Israel, Facsimile: +972-4-627 5598, or visit Itamar’s web
site at www.itamar-medical.com.

APPENDIX D: REGULATORY REPRESENTATIVE
Itamar Medical’s authorized regulatory representative is:
MEDES Ltd.
5 Beaumont Gate, Shenley Hill,

Radlett, Hertfordshire WD7 7AR.
England
Tel: +44 208123 8056
Tel / Fax: +44 1923859810

APPENDIX E: DESCRIPTION OF THE WATCHPAT™200U UPAT
PROBE
The WatchPAT uPAT probe is an opto-pneumatic finger-mounted probe.

Its role is to continuously measure the relative state of the vasomotor activity in the distal
part of the finger based on a plethysmographic method. The uPAT probe is designed to
cover the distal part of the finger with a uniform pressure field extending to the tip of the
finger. This design prevents venous blood pooling, engorgement and stasis, which inhibits
retrograde venous shock wave propagation, and allows partial unloading of arterial wall
tension that significantly improves the dynamic range of the measured signal. The optic
component of the probe measures the optical density related changes of the arterial blood
volume in the digital arteries, associated with each heartbeat. Peripheral arterial
constrictions, when present, are shown by attenuation in the PAT signal amplitude, a
marker of sympathetic activation.
The uPAT probe also measures the changes in absorbance of the finger at both red and
infrared light at peak wavelengths of 660nm and 910nm respectively. The maximum
optical output power is 65mW. These measurements are used to calculate the oximetry
signal in an offline program according to the pulse oximetry principles.
The uPAT probe is an integral part of the WatchPAT™ device and is to be used only with
the WP200U device.

APPENDIX F: MANUFACTURING DECLARATIONS ACCORDING
TO IEC 60601-1-2
Electromagnetic Compatibility
Notes
• The WatchPAT™200U (WP200U) requires special precautions with regard to electromagnetic
compatibility.
• It must be installed and prepared for use as described in section 11 - Preparation for Sleep Study.
• Certain types of mobile telecommunication devices such as mobile telephones are likely to
interfere with the WP200U.
• The recommended separation distances in this section must therefore be complied with.
• The WP200U must not be used near or on top of another device. If this cannot be avoided, it is
necessary – before clinical use – to check the equipment for correct operation under the conditions
of use.
• The use of accessories other than those specified or sold by Itamar Medical as replacement parts
may have the consequence of increasing the emissions or decreasing the immunity of the unit.
Electromagnetic Emissions
 WP200U is intended for use in the electromagnetic environment specified in the following tables 1,
2, 4 and 6 below.
• The user and/or installer of the unit must ensure that it is used in such an environment.
Table 1 – from IEC 60601-1-2:2007

Guidance and manufacturer's declaration – electromagnetic emissions – WP200U
The WP200U is intended for use in the electromagnetic environment specified below; The customer or the user of the WP200U
should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance

RF emissions The WP200U uses RF energy only for its internal function. Therefore, its RF
Group 1 emissions are very low and are not likely to cause any interference in nearby
CISPR 11 electronic equipment.
RF emissions
Class B
CISPR 11
Harmonic emissions
The WP200U is suitable for use in all establishments, including domestic
Class B
establishments and those directly connected to the public low-voltage power
IEC 61000-3-2 supply network that supplies buildings used for domestic purposes.
Voltage fluctuations/
flicker emissions
Complies
IEC 61000-3-3

Table 2 - from IEC 60601-1-2:2007
Guidance and manufacturer's declaration – electromagnetic immunity – WP200U
The WP200U is intended for use in the electromagnetic environment specified below; The customer or the user of the WP200U
IEC 60601-1-2
Immunity test Compliance level Electromagnetic environment - guidance
Test level
 
Electrostatic 6 kV contact 6 kV contact
discharge (ESD) IEC
61000-4-2 8 kV air 8 kV air
 
Electrical fast 2 kV for power 2 kV for power
Mains power quality should be that of a typical public
transient/burst supply lines supply lines
low-voltage power supply network that supplies
buildings used for domestic purposes, commercial or
1 kV for input/output ot Applicable hospital, clinic environment.
IEC 61000-4-4 lines
 
Surge 1 kV differential 1 kV differential Mains power quality should be that of a typical public
mode mode low-voltage power supply network that supplies
buildings used for domestic purposes, commercial or
IEC 61000-4-5 2 kV common mode 2 kV common mode hospital, clinic environment.
Voltage dips, short <5 %UT <5 %UT Mains power quality should be that of a typical public
interruptions and (>95 %dip in UT) (>95 %dip in UT) low-voltage power supply network that supplies
voltage variations for 0,5 cycle for 0,5 cycle buildings used for domestic purposes, commercial or
on power supply hospital, clinical environment.
input lines 40 %UT 40 %UT If the user of the WP200U requires continued
(60 %dip in UT) (60 %dip in UT) operation during power mains interruptions; it is
for 5 cycles for 5 cycles recommended that WP200U be powered from a
IEC 61000-4-11 <5 %UT <5 %UT separate power supply (UPS, etc.).
. 70 %UT 70 %UT
(30 %dip in UT) (30 %dip in UT)
for 25 cycles for 25 cycles
<5 %UT <5 %UT
<5 %UT <5 %UT

(>95 %dip in UT) (>95 %dip in UT)
for 5 s for 5 s
Power frequency 3 A/m 3 A/m Power frequency magnetic fields should be at levels
(50/60 Hz) characteristic of a typical public low-voltage power
magnetic field supply network that supplies buildings used for
domestic purposes, commercial or hospital, clinic
IEC 61000-4-8 environment.
NOTE: UT is the a.c. mains voltage prior to application of the test level.

Table 4 - from IEC 60601-1-2:2007
Guidance and manufacturer's declaration – electromagnetic immunity – WP200U
The WP 200U is intended for use in the electromagnetic environment specified below; The customer or the user of the WP200U
IEC 60601-1-2
Compliance
Immunity test Electromagnetic environment - guidance
level
Test level
Portable and mobile RF communications equipment
should be used no closer to any part of the
WP200U, including cables, than the
recommended separation distance calculated from
the equation applicable to the frequency of the
transmitter
.
Recommended separation distance
d = 1.17√P
Conducted RF 3 Vrms 3 Vrms
IEC 61000-4-6 150 k Hz to 80 MHz

d = 1.17√P 80 M Hz t o 800 MHz
Radiated RF 3 V/m 3 V/m

d= 2.3√P 800 MHz t o 2,5 GHz
IEC 61000-4-3 80 MHz to 2,5 GHz
where P i s the maximum output power rating of the

transmitter in watts (W)according to the transmitter
manufacturer and d i s the recommended separation
Distance in meters (m).
Field strengths from fixed R F transmitters, as

determined by an electromagnetic site survey ,a should be
less than the compliance level in each frequency
range .d
Interference may occur in the vicinity of equipment

marked with the following symbol:
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations .Electromagnetic propagation is affected by absorption
And reflection from structures objects and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, 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 WP200U is used exceeds the applicable RF compliance level above, the WP200U should
be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-
orienting or relocating the WP200U.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

Recommended Separation Distances
The WP200U is intended for use in an electromagnetic environment in which radiated

radiofrequency disturbances are controlled.
The user and/or installer of the unit can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile radiofrequency communications equipment
(emitters) and the WP200U, according to the maximum output power of the equipment, as
recommended in the table below.
Table 6 - from IEC 60601-1-2:2007

Recommended separation distances between
portable and mobile RF communications equipment and the WP200U
Separation distance according to frequency of transmitter (in meters)
Rated maximum output power Meters [m]

of transmitter
150kHz to 80MHz 80MHz to 800MHz 800MHz to 2.5GHz
Watts [W]
d = 1.17√P d = 1.17√P d= 2.3√P
0.01 0.12 0.12 0.23

0.1 0.37 0.37 0.73
1 1.17 1.17 2.3
10 3.7 3.7 7.3
100 11.7 11.7 23
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 80 MHz and 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 absorption and reflection from
structures, objects, and people.

APPENDIX G: SPO2 ACCURACY IN THE WATCHPAT™200U
The WatchPAT™200U device uses Itamar Medical Pulse Oximetry system for the
measurement of functional oxygen saturation of arterial haemoglobin (SpO2). This
appendix includes information regarding the accuracy of these measurements following a
clinical study of Itamar Medical Pulse Oximetry.
1. Overall, the Arms is estimated to be 2.1 for the range 70-100%
2. The next table shows SpO2 Accuracy Results:
Test Device SpO2 67-100% SpO2 90-100% SpO2 80-90% SpO2 70-80%
ARMS / Bias ARMS / Bias ARMS / Bias ARMS / Bias
WatchPAT™200U
Finger Sensor Set ARMS 2.1 (726 pts) ARMS 1.4 (255 pts) ARMS 1.9 (227 pts) ARMS 2.7 (225 pts)
2 – H series Bias 0.6 Bias -0.6 Bias 0.9 Bias 1.5
3. The next table shows the Bland-Altman plot for Itamar-Medical WP200U:

Reference: CO-Oximetry Range 68-99%
Linear Regression (Bland Altman) y = -0.0931x + 8.7875
Mean Bias 0.51
# pts 726
Upper 95% Limits of Agreement 4.3
Lower 95% Limits of Agreement -3.3
*Source of data:
Title: Itamar SpO2 Accuracy Validation vs Reference CO-
Oximetry, PR2013-062
Date: 2013-08-20
Clinical Investigator(s): Clinimark
80 Health Park Drive, Suite 20
Louisville, Colorado 80027, USA
Sponsor: Itamar Medical, Ltd. 9 Halamish St POB 3579, Caesarea
3088900 Israel
Device(s): Non-Motion: Itamar Medical WatchPAT 200 Pulse Oximetry
Study Date(s): May 8-10, 2013
Note
A Functional tester cannot be used to assess the accuracy of the internal

pulse oximeter.

APPENDIX H: TRAINING RESOURCES
WatchPAT™ device training materials can be found and downloaded from:

www.itamar-medical.com/training
These files can also be viewed through any smartphone running QR code reader or optical
scanner application, by scanning the code next to each resource.
The following resources can be found on this page:
Technician Training Presentation
Step-by-Step Card – English
zzzPAT User Manual
WatchPAT™ Device Patient Video
zzzPAT Manual Editing of Sleep Scoring

APPENDIX I: SPARE PARTS LIST
The following items can be ordered and purchased individually:
 uPAT probe (a box of 12 uPAT probes)

 uPAT probe connection cable
 Wrist Strap
 Snore and Body Position sensor
 Adhesive for Snore and Body Position sensor (a package of 12 units)
 Cable for Tamper-Proof Bracelet
 Tamper-Proof Bracelet (a box of 24 bracelets)
 AC adapter
 USB cable
 Rechargeable Lithium Ion Battery
 Step-by-Step Reference Guide WP200 Unified + Itamar SBP
 Quick Reference Cards WP200 Unified
 Carrying case

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WatchPAT™200 Unified

Itamar Medical REF OM2196335

Copyright  2015 By Itamar Medical Ltd.

Itamar Medical Ltd.

ISO 9001:2008 and EN ISO 13485:2012

WatchPAT™200U System i Operation Manual

Edition Date Description Chapter Pages Resp.

WatchPAT™200U System ii Operation Manual

1 GENERAL INFORMATION ..................................................... 1

WatchPAT™200U System iii Operation Manual

WatchPAT™200U System iv Operation Manual

WatchPAT™200U System v Operation Manual

1.1 Intended Use / Indications for Use

1.2 Restrictions for Use

WatchPAT™200U System 1 Operation Manual

1.3 Exclusion Criteria

1.4 Data Generated by the WatchPAT™200U

1.5 Equipment Classification

WatchPAT™200U System 2 Operation Manual

WatchPAT™200U System 3 Operation Manual

1.7 CE and CSA Compliance

The product complies with MDD 93/42 EEC: 1993 &

The product is certified by CSA.

1.8 Conventions Used in this Manual

Warnings are used to identify conditions or actions, which - if the

Les avertissements sont utilises pour identifier les conditions ou les

WatchPAT™200U System 4 Operation Manual

Les précautions sont utilisées affin d’identifier les conditions ou les

Notes are used to identify an explanation, or to provide additional

1.9 Warnings, Cautions and Notes

WatchPAT™200U System 5 Operation Manual

WatchPAT™200U System 6 Operation Manual

Follow instructions for use

Type BF applied part

The product is certified by CSA

The product is marked with the CE logo

Single use, do not re-use

Medical device Manufacturer

IP22 Ingress protection

WatchPAT™200U System 7 Operation Manual

1.12 WatchPAT™200U Device Labels

Located on WatchPAT™200U device

Located on WatchPAT™200U device

1.13 FDA information

WatchPAT™200U System 8 Operation Manual

WatchPAT™200U System 9 Operation Manual

WatchPAT™200U System 10 Operation Manual

Optional Snore & Body

Figure 2 – WatchPAT™200U Device with Sensors

2.2 User Interaction with the WatchPAT™ Device Keys

WatchPAT™200U System 11 Operation Manual

Figure 3 – The Buttons and Display

Service Ports and Peripherals

WatchPAT™200U System 12 Operation Manual

uPAT probe port

USB port for charging

Figure 4 – Service Ports and Peripherals

Figure 5 – WatchPAT™ Wrist Strap

2.3 WatchPAT™ Device Function

WatchPAT™200U System 13 Operation Manual