CM676A91343-60091343-05, 91347-05

Exhibit G: User Manual 1 FCC ID: CM676A91343-600 Page 1 of 6 Ultraview Digital Telemetry 91341, 91343, 91347, 90478, 90479-A
Operation in the Wireless Medical Telemetry Service (WMTS) bands (608-614, 1395-1400, 1427-1429.5, 1429-1431.5 MHz).
Approved to operate under FCC Part 95 rules.
ECG and multiparameter transmitter.
ECG, SpO 2 , and NIBP (optional) for ambulatory patients.
Touchscreen control of all module functions and compatible with all Ultraview Care Network ™ monitors.
Lightweight, water resistant transmitters.
Tunable transmitters.
Diversity antenna system.
Tunable modular receiver.
Modular receiver converts bedside monitors to telemetry operation.
Multi-lead ECG with ST segment analysis option; comprehensive arrhythmia and ST trending.
Module Configuration Manager enables the hospital to customize the receiver’s ECG patient monitoring functions to specific patient populations, clinical protocols, or operating preferences.
Graded alarm functions enables the hospital to define high, medium, or low alarm tones according to critical, warning, or advisory event severity.
Expanded central monitoring of ambulatory patients outside central antenna coverage. Diversity Antenna System 90217 ABP Monitor 90478 Modular Receiver Receiver Housing 91343 Digital Telemetry Multiparameter Transmitter 91341/47 Digital Telemetry ECG Transmitters 90479-A Modular Ultraview 1030/1050 ® SPECIFICATIONS Ultraview Digital Telemetry 91341, 91343, 91347, 90478, 90479-A Page 2 of 6 PARAMETER CHARACTERISTICS ECG Maximum Input — ±4 mV ( ±10%) DC Offset — Up to ±300 mV, with no more than 2% signal amplitude degradation Overdrive Recovery Time — < 1 second circuit settling time with offset voltage < 500 mV Noise — < 30 μV p-v, refered to input (rti), at 30 Hz bandwidth CMRR — > 85 dB (monitor mode) QRS Detection — Detects QRS complexes with durations of 40 to 120mS and amplitudes of 0.2 to 4.0 mV (adult) or 0.15 to 4.0 mV (neonatal) Defibrillator Protection — Meets IEC 60601-2-27, AAMI EC-13 Resolution — 2.5 μV per LSB, rti Input Impedance — > 10 MΩ minimum differential at 10 Hz Gain Accuracy — ±5% Pacer Rejection — Baseline shift < 0.2 mV (measured at ECG x 1,000 output) Pacer Detection — Detects pacer pulses of ±2 mV to ±700 mV with pulse widths of 0.2 to 2 msec and rise times 10% of width not to exceed 100 μsec. Signal Bandwidth — 0.05 to 30 Hz ±10% (-3 dB) Sample Rate — 120 samples per second SpO 2 SpO 2 Sensor Interface — Red LED drive (max): 175 mA peak at 10% duty cycle IR LED drive (max): 105 mA peak at 10% duty cycle SpO 2 Measurement Method — Functional saturation (oxygen saturation of functional hemoglobin). SpO 2 Measurement Mode — Continuous, episodic (2 minutes, 5 minutes, and 30 minutes) sampling intervals; factory default setting is continuous. ST Segment Analysis Resolution — 0.08 mm Range — ±9 mm (1 mV = 10 mm) Leads — ST Segment Analysis continously performed on up to seven leads. Alarms — Single lead or multiple leads; individual leads can be deselected. Alarms for absolute minimum and maximum ST levels; changes in ST level over the last 5 minutes. Displays — ST values: minimum/maximum/ current ST segment deviation and 5 minute averaged segments for the last 30 minutes. Measurement Points — Adjustable ST, PR, and J Points Trends — Up to 24 hours of trend data can be displayed in 1.5-, 3-, 6-, 12-, or 24-hour time tracks. PATIENT MONITOR DISPLAY CHARACTERISTICS ECG Display Heart Rate Range — 30 to 300 bpm; heart rates > 300 bpm are displayed as “+++”. Heart Rate Alarm Limits — High: 5 to 300 bpm, Low: 0 to 200 bpm; alarms automatically enabled over a range of 40 (adult) or 100 (neonatal) to 300 bpm; heart rates > 300 bpm are displayed as “+++”. Accuracy — ±1% or ±2 beats per minute (whichever is greater). Numeric Update Rate — Every 3 seconds or immediately at the onset of an alarm. Trace Sweep Speeds — 50, 25, 12.5 mm/sec Display Bandwidth — Two settiings: 0.5 to 30 Hz ±10% (-3 dB) in monitor mode, and 0.05 to 30 Hz ±25% (-3 dB at 50 mm per second) in extended mode. SpO 2 Display Measurement Range — 30 to 100% O 2 Saturation Saturation Accuracy — Sensor Dependent Saturation Resolution — ±1% Pulse Rate Range — 30 to 250 bpm Pulse Rate Resolution — 1 bpm Alarms — High and low saturation values; factory default limits are: high 100%; low 85%. High range: 31% – 100% Low range: 30% – 99% Numeric Update Rate — Every 2 seconds for continuous SpO 2 readings. SPECIFICATIONS Ultraview Digital Telemetry 91341, 91343, 91347, 90478, 90479-A Page 3 of 6 NIBP Display (Refer to specifications for the 90217 ABP Monitor) Measurement Range (adult only) — Systolic:8.0 – 35.0 kPa (60 – 260 mmHg) Diastolic:9.0 – 27.0 kPa (30 – 200 mmHg) Mean:5.3 – 31.0 kPa (40 – 230 mmHg) Pressure Accuracy — ±2% or ±3 mmHg (whichever is greater) Resolution — 1 mmHg Time Between Readings — selectable, from 6 to 120 minutes Alarms — High and low alarms for all measured parameters. High range: 8.0 – 35.0 kPa (60 – 260 mmHg) Low range: 4.0 – 27.0 kPa (30 – 200 mmHg) TRANSMITTERS (91341, 91343, 90347) ECG Transmission — View 2 of 7 available leads from two vectors (91341) or four vectors (91343, 91347) synchronized RF digital signal. Electrode Configuration — Individually replaceable DIN standard safety lead wires. Local lead fault indicators for each lead wire. Multiparameter Transmission (90343) — SpO 2 (saturation, SpO 2 sensor status, pulse rate) and optional NIBP (systolic, diastolic, mean pressure, measurement time, alarm conditions) with the model 90217 ABP monitor. Additional Data Transmitted — Patient record, low battery indicator, pacer flag, patient ID code, and electrode connection status. Output Power — 1 mW ERP, typical Spectral Efficiency — 0.11 bps/Hz External Indicator — Yellow LED flashes when battery level is low Battery — 9 V battery; refer to Table 1 for battery life expectancy WMTS Frequency Band Option — -05:608-614 MHz -09:1395-1400 MHz 1427-1429.5 MHz 1429-1431.5 MHz Transmitter Physical Dimensio…

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Exhibit H: User Manual 2 FCC ID: CM676A91343-600 Ultraview Digital Telemetry 91341 / 91343 / 91347 Operations Manual 071-0774-00 Rev. A ® Copyright 2002 Spacelabs Medical, Inc. All rights reserved. Contents of this publication may not be reproduced in any form without the written permission of Spacelabs Medical, Inc. Products of Spacelabs Medical are covered by U.S. and foreign patents and/or pending patents. Printed in U.S.A. Specifications and price change privileges are reserved. Spacelabs Medical considers itself responsible for the effects on safety, reliability and performance of the equipment only if: •assembly operations, re-adjustments, modifications or repairs are carried out by persons authorized by Spacelabs Medical, and •the electrical installation of the relevant room complies with the requirements of the standard in force, and •the equipment is used in accordance with the operations manual. Spacelabs Medical will make available, on request, such circuit diagrams, component part lists, descriptions, calibration instructions or other information which will assist appropriately qualified technical personnel to repair those parts of the equipment which are classified by Spacelabs Medical as field repairable. Spacelabs Medical, Inc. 15220 N.E. 40th Street P.O. Box 97013 Redmond, WA 98073-9713 U.S.A. Telephone: 425-882-3700 Fax: 425-885-4877 Telex: 4740085 SPL UI Spacelabs Medical Products Pty. Ltd. Macquarie View Estates Unit 1, 112-118 Talavera Road North Ryde, N.S.W. 2113 AUSTRALIA Telephone: 61-2-9878-6644 Fax: 61-2-9878-4820 Spacelabs Medical Products GmbH Jochen Rindt Straße 25 1230 Vienna AUSTRIA Telephone: 43-1-616 52 37 Fax: 43-1-616 52 37 11 Spacelabs Medical B.V. Airport Boulevard Office Park Bessenveldstraat 25A 1831 Diegem BELGIUM Telephone: 32 2 7164026 Fax: 32 2 7164114 Spacelabs Medical Products, Ltd. 151 Superior Boulevard, Unit 1 Mississauga, Ontario L5T 2L1 CANADA Telephone: 905-670-5880 Fax: 905-670-5883 CORPORATE OFFICES Spacelabs Medical Instruments (Tianjin) Co. Ltd. 6th Floor, Wang Jing Building 9 Wang Jing Zhong Huan South Road Cho Yang District, Beijing 100015 CHINA Telephone: 86-10-64731705 Fax: 86-10-64721707 Authorized EC Representative: Spacelabs Medical Sarl 6, Allée des Saules Europarc 94042 Créteil Cedex FRANCE Telephone: 33 (0) 1 45.13.22.44 Fax: 33 (0) 1 45.13.22.00 Spacelabs Medical GmbH Airport Park Willicher Damm 121+123 41066 Mönchengladbach GERMANY Telephone: 49-2161-8209-0 Fax: 49-2161-8209-222 Spacelabs Medical Limited Suite 901 Tower 1 China Hong Kong City 33 Canton Road, Tsimshatsui Kowloon HONG KONG Telephone: 852-2376-1370 Fax: 852-2376-2502 Spacelabs Medical, Inc. c/o Impulse Business Club F-22 South Extension Part 1 New Delhi 110049 INDIA Telephone: 911 1464 5002 Fax: 911 4603338 Spacelabs Medical S.r.l. Via Montecatini, 13 20144 Milano ITALY Telephone: 39-0-2/48958203 Fax: 39-0-2/48958204 Spacelabs Medical Ltd. 2F-3, No. 161. Sung Te Road Taipei, Taiwan R.O.C. TAIWAN Telephone: 8862-2759-7238 Fax: 8862-2759-9060 Spacelabs Medical B.V. Ringveste 9 A 3992 DD Houten THE NETHERLANDS Telephone: 31-(0)-30-638 5050 Fax: 31-(0)-30-638 5059 Spacelabs Medical Ltd. Indigo Building Unit 9, Mulberry Business Park Fishponds Road Wokingham, Berkshire RG 41 2GY UNITED KINGDOM Telephone: 44 118 9773 100 Fax: 44 118 9798 200 CAUTION: •US Federal law restricts the devices documented herein to sale by, or on the order of, a physician. Spacelabs Medical is committed to providing comprehensive customer support beginning with your initial inquiry through purchase, training, and service for the life of your Spacelabs Medical equipment. If you need our help along the way, we offer these guidelines for fast, efficient response. Acquiring Equipment Sales Representative 800-522-7025 (U.S.A.) or call your local office To discuss your monitoring or clinical information needs, to schedule product demonstrations, to order equipment, or to schedule in-service education Delivery Information 800-251-9910 (U.S.A.) or call your local office To find out when you can expect delivery of your Spacelabs Medical equipment Supplies Products 800-223-6467 (U.S.A.) or call your local office To order compatible supplies and accessories for your equipment Getting Started Sales Representative 800-522-7025 (U.S.A.) or call your local office To arrange in-service education sessions Answering Other Needs Clinical Applications 800-522-7025 (U.S.A.) or 425-882-3700 or call your local office To answer specific questions on arrhythmia products and clinically related issues First Call SM National Dispatch Center 800-522-7025 (U.S.A.) 800-942-7968 (Canada) To call for service or to contact your assigned customer service representative Technical Support - Monitoring/Anesthesia 800-522-7025 (U.S.A.) or 425-882-3700 or call your local office For technical support of all Ultraview ® Care Network ™ monitoring products and anesthesia products Technical Support - Intesys Clinical Information Systems 800-210-0247 (U.S.A.) or 425-882-3700 or call your local office For technical support of BirthNet ® , Caremaster ® , Chartmaster ® , QuIC, and WinDNA ® products Service Parts Department 800-547-8805 (U.S.A.) or 425-867-2039 or call your local office For parts ordering and pricing information Service Training Department 800-251-9910 (U.S.A.) or call your local office To arrange training of hospital biomedical and anesthesia personnel Regional Service Manager 800-522-7025 (U.S.A.) 800-942-7968 (Canada) or call your local office To obtain answers to general questions concerning service issues and service contracts Contacting Your Local Offices Outside the U.S. Mississauga, Ontario Canada 905-670-5880 Mönchengladbach Germany 49-2161-8209-0 Kowloon Hong Kong 852-2376-1370 Taipei Taiwan 8862-2759-7238 Créteil France 33 (0)1 45.13.22.44 Vienna Austria 43-1-616 52 37 Milano Italy 39-0-2/48958203 Beijing China 86-10-64731705 Wokingham, Berkshire U.K. 44 118 9773 100 New Delhi India 911 1464 5002 Diegem Belgiu…

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Exhibit J: Request for Confidentiality Letter FCC ID: CM676A91343-600

NORTHWEST EMC, INC. 22975 NW Evergreen Parkway, Suite 400 Hillsboro, OR 97124 July 26, 2002 Dear Application Examiner: On behalf of Spacelabs Medical, Northwest EMC, Inc is submitting this application for the certification of Models 91343-05 and 91347-05 Digital Telemetry Transmitters, FCC ID: CM676A91343-600. Both models are biomedical telemetry transmitters that operate in the 608-614 MHz band. Both use identical radios and antennas. The only difference is the 91343-05 has additional patient cables. The technical report and exhibits included with this application demonstrate compliance with FCC rules 47 CFR 95.1115. Your efforts in reviewing this application are greatly appreciated. Best regards, Greg Kiemel Northwest EMC, Inc.

Exhibit B: External Photos FCC ID: CM676A91343-600 91347-05 Back View 91347-05 Front View

Exhibit B: External Photos FCC ID: CM676A91343-600 91343-05 Back View 91343-05 Front View

Exhibit A: FCC ID Label and Location FCC ID: CM676A91343-600

Exhibit A: FCC ID Label and Location FCC ID: CM676A91343-600

Exhibit C: Internal Photos FCC ID: CM676A91343-600 Transmitter Board Top View Transmitter Board Bottom View Interior View of 600 MHz ECG

Exhibit C: Internal Photos FCC ID: CM676A91343-600 Transmitter Board Top View Transmitter Board Bottom View Interior View of 600-1400 MHz MPT

Exhibit I: Operational Description FCC ID: CM676A91343-600 Operational Description The 91341-05 is a battery-powered portable electrocardiogram (ECG)-only transmitter operating on a 25 kHz channel scheme in the 608 – 614 MHz band. The Telemetry Transmitter is a low-power device that is worn continuously by a patient. Patient physiological parameters are monitored and transmitted via radio frequency (RF) to a fixed antenna network. The antenna network feeds a receiver, which processes the data and forwards it to a central monitor for display. The telemetry transmitter is intended to be used on the orders of a physician and limited to the confines of a healthcare facility. It is not for vehicle use outside the healthcare facility. The 91343-05 is a battery-powered portable multi-parameter (ECG and SPO2) transmitter and the 91347- 05 is a wideband electrocardiogram (ECG)-only transmitter. Both operate on a 50 kHz channel scheme in the 608 – 614 MHz band. The 91343-05 is also equipped with an Infrared (IR) interface that accepts data from compatible devices to forward other patient information to the central monitor. The Telemetry Transmitters are low-power devices that are worn continuously by a patient. Patient physiological parameters, such as heart rate and pulse oximetry, are monitored and transmitted via radio frequency (RF) to a fixed antenna network. The antenna network feeds a receiver, which processes the data and forwards it to a central monitor for display. The telemetry transmitter is intended to be used on the orders of a physician and limited to the confines of a healthcare facility. It is not for vehicle use outside the healthcare facility. Wideband (50 kHz) Channel #Frequency (MHz) 2242608.0375 2244608.0875 2246608.1375 2248608.1875 2250608.2375 2252608.2875 2254608.3375 2256608.3875 2258608.4375 2260608.4875 2262608.5375 2264608.5875 2266608.6375 2268608.6875 2270608.7375 2272608.7875 2274608.8375 2276608.8875 2278608.9375 2280608.9875 2282609.0375 2284609.0875 2286609.1375 2288609.1875 2290609.2375 2292609.2875 2294609.3375 2296609.3875 2298609.4375 2300609.4875 2302609.5375 2304609.5875 2306609.6375 2308609.6875 2310609.7375 2312609.7875 2314609.8375 2316609.8875 2318609.9375 2320609.9875 2322610.0375 2324610.0875 2326610.1375 2328610.1875 2330610.2375 2332610.2875 Channelization Scheme Channel #Frequency (MHz) 2334610.3375 2336610.3875 2338610.4375 2340610.4875 2342610.5375 2344610.5875 2346610.6375 2348610.6875 2350610.7375 2352610.7875 2354610.8375 2356610.8875 2358610.9375 2360610.9875 2362611.0375 2364611.0875 2366611.1375 2368611.1875 2370611.2375 2372611.2875 2374611.3375 2376611.3875 2378611.4375 2380611.4875 2382611.5375 2384611.5875 2386611.6375 2388611.6875 2390611.7375 2392611.7875 2394611.8375 2396611.8875 2398611.9375 2400611.9875 2402612.0375 2404612.0875 2406612.1375 2408612.1875 2410612.2375 2412612.2875 2414612.3375 2416612.3875 2418612.4375 2420612.4875 2422612.5375 2424612.5875 2426612.6375 2428612.6875 2430612.7375 2432612.7875 Channel #Frequency (MHz) 2434612.8375 2436612.8875 2438612.9375 2440612.9875 2442613.0375 2444613.0875 2446613.1375 2448613.1875 2450613.2375 2452613.2875 2454613.3375 2456613.3875 2458613.4375 2460613.4875 2462613.5375 2464613.5875 2466613.6375 2468613.6875 2470613.7375 2472613.7875 2474613.8375 2476613.8875 2478613.9375 2480613.9875 Antenna Information The Tecom Patch Antenna, Part Number 823951 is integral to the unit (laminated under the label on the face) and is not user-accessible. It is specified for a max. peak gain of 0 dBi, an average gain of -4dBi; and input VSWR of less than 2.0:1. The input impedance is a nominal 50 ohms. The antenna uses a micro-coaxial cable permanently soldered to the foil. The other end of the cables has a connector that is attached to the 50 ohm output of the RF PCBA. Modulation and Channelization Modulation Type: FM - Two Level FSK Modulating Signal: Data Signal: 0 to 5volts Maximum Frequency: 4.096KHz Wide Band Maximum Data Rate: 8.192KHz Wide Band Modulation Index: 0.488 Wide Band Channel Spacing: 50 kHz Wide Band Duty Cycle: 100% Communication Protocol Custom to Spacelabs The modulation and channelization are controlled by a micro-controller on the transmitter board. This micro-controller reads the channel switch settings and programs the synthesizer with the appropriate register settings to lock to the desired channel. The micro-controller also controls three digital potentiometers that are responsible for setting the deviation of the FM modulation and the fine tuning of the center frequency. These potentiometer settings are calibrated during manufacturing and stored in flash memory. Two of the potentiometers adjust the voltage levels presented to the control pin of the synthesizer's crystal reference. The other potentiometer adjusts the voltage levels presented to the VCO's varactors. The RF output is turned off when the channel switch settings are invalid, when the VCO is unlocked, or when the battery voltage drops below 5.3V.

Exhibit R: Justification for Emission Designator FCC ID: CM676A91343-600 CM676A91343-600 Justification for Emission Designator Emission Classification Per 47 CFR 95.1115 (c), the EUT complies with the requirement that “a wireless medical telemetry device may transmit any emission type appropriate for communications in this service, except for video and voice. Waveforms such as electrocardiograms (ECGs) are not considered video.” The EUT has F1D emission. The EUT uses a digital, frequency shift keying modulation scheme with no sub-carriers. The emission designator “F1D” was selected based upon the guidelines in 47 CFR 2.201: “F” designates an emission in which the main carrier is frequency modulated. “1” designates a single channel containing digital information without the use of a modulating sub-carrier (the applicant confirmed that no sub-carriers are used). “D” designates data transmission, telemetry. As detailed in the user manual, the device is used to transmit non-voice, non-video, biomedical telemetry. Necessary Bandwidth Per 47 CFR 2.202(c), the necessary bandwidth is calculated using Carson’s Rule: 2M + 2D = 2(12290) +2(6000) = 36.58 kHz. Where “M” is equal to the EUT’s maximum modulation frequency in Hertz, and D is equal to the EUT’s peak frequency deviation (i.e. half the difference between the maximum and minimum values of the instantaneous frequency). Per 47 CFR 2.202(b), the necessary bandwidth is expressed “by three numerals and one letter. The letter occupies the position of the decimal point and represents the unit bandwidth”. The EUT's necessary bandwidth is expressed as “36K6” Hence the EUT’s emission designator is “36K6F1D”.

Exhibit F: Tune-up Procedure FCC ID: CM676A91343-600 Only information regarding operation at 608-614 MHz applies. Transmitter Tune-up Procedure at a specified power range. The 600MHz and 1400MHz transmitters are designed to operate at one power level and within the RF output power limits shown in the table below. There are no adjustments for changing the RF output power level either in the factory or by the end user. Subject Specifications Comments Frequency Range 600 MHz model 608.0 – 614.0 MHz 1400 MHz model 1395 – 1400 MHz 1427 – 1432 MHz 1400 – 1427 is a restricted band. Radio should never transmit into this band or outside the bands normally operated. Modulation FM – FSK 2-level Access Method FDMA –Transmit only Transmit Power (RMS CW) Conducted (50 Ω Load) 600 MHz Band 1400 MHz Band 3.0 dBm +/-3dB 6.0 dBm +1dB -3dB Assumes 3dB ground bounce, 0dB peak antenna gain. FCC limit = 10.8 dBm @ 600 MHz, 22.2 dBm @ 1400 MHz For 1400 MHz 6.0 dBm max was chosen to conserve battery power. For an analysis of the predicate design transmit performance see System Design Document Rev2. Murandi Communications Ltd. Innovative Radio Frequency Solutions Murandi Communications Ltd.Suite 240, 6715 - 8th St. NE, Calgary, Alberta, Canada, T2E 7H7 Tel: (403) 777-9988Fax: (403) 777-9989 RF Control and Operation for the Medical Telemetry Transmitter Rev2 – July/01 1. Table of Contents 1.Table of Contents............................................................................................................1 2.Reference Documents.....................................................................................................1 3.Revision Notes................................................................................................................1 4.Introduction.....................................................................................................................1 5.Power Up........................................................................................................................1 5.1Invalid Channel............................................................................................................2 6.User Channel Selection....................................................................................................2 7.Transmitter type..............................................................................................................3 2. Reference Documents 1. Spacelabs System Design for the Medical Telemetry Transmitter- Draft, July,2001 2. Spacelabs Technical Specification for the Medical Telemetry Transmitter, Rev 1,2001 3. Revision Notes July 16,2001Changed document to Rev1 July 16,2001Changed “Programming the Synthesizer” to “User Channel Selection” July 30,2001Changed document to Rev2 July 30,2001Added Sec 5.1 , Invalid Channel 4. Introduction This document details how the RF deck is controlled and operated. There are 2 high level functions: • Power up • Programming the synthesizer These high level functions are presented below. 5. Power Up The RF deck operates autonomous to the rest of the unit. To power up the unit all that is required is connection of a 9V battery, the unit will automatically set all it’s conditions to transmit within a certain amount of time, defined in the technical specification. It is designed in this way to provide live data transmission only, no other mode of operation exists. RF Control and OperationPage 2Printed: 13/08/01 2:53 PM Murandi Communications Ltd.Suite 240, 6715 - 8th St. NE, Calgary, Alberta, Canada, T2E 7H7 Tel: (403) 777-9988Fax: (403) 777-9989 5.1 Invalid Channel When reading the channel selection from the Dip-switches the microcontroller will perform a check for validity. On the condition that the settings are invalid the microcontroller will program unlockable data into the synthesizer, preventing transmission on an unknown channel. During power up the microcontroller reads and stores the Dip-switch settings on board, no changes to the switches following this will affect transmit in any way, until the unit is powered off, then back on. In the event of a reset or loss of Lock Detect, the microcontroller will reload data stored internally in FLASH memory and reprogram all possibly affected devices. In the event that the synthesizer registers programming changes during operation, it is expected that the synthesizer will lose lock at least momentarily if not permanently. This will prompt the microcontroller to reset and reprogram the synthesizer. 6. User Channel Selection Programming the synthesizer takes place each time the PWT is powered up. This operation is automatically completed by the microcontroller to enable the correct frequency for transmission. The required data to program the synthesizer is translated from the two – 8pin dipswitches (in the form of a channel selection) to the necessary code for frequency setting. This operation takes place only when the unit is powered up. For the switch settings to take effect the unit must be powered off, then back on. The following tables illustrates the switch settings for each channel and the corresponding frequency. 600MHz Band (WideBand)SW2SW1600MHz Band (NarrowBand)SW2SW1 ChannelRF Frequency (MHz)432187654321ChannelRF Frequency (MHz)432187654321 2242608.03751000110000101241608.0125010011011001 2244608.08751000110001001242608.0375010011011010 2246608.13751000110001101243608.0625010011011011 2248608.18751000110010001244608.0875010011011100 2250608.23751000110010101245608.1125010011011101 2252608.28751000110011001246608.1375010011011110 2254608.33751000110011101247608.1625010011011111 2256608.38751000110100001248608.1875010011100000 2258608.43751000110100101249608.2125010011100001 2260608.48751000110101001250608.2375010011100010 2262608.53751000110101101251608.2625010011100011 2458613.43751001100110101470613.7375010110111110 2460613.48751001100111001471613.7625010110111111 2462613.53751001100111101472613.7875010111000000 2464613.5875100110100000147361…

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Exhibit L: RF Exposure FCC ID: CM676A91343-600 RF Exposure statement provided by client: This section is not applicable. The FCC, with full knowledge that patients within a healthcare facility wear these devices continuously in close proximity to the body, determined field strength limitations on transmitters operating in the Wireless Medical Telemetry System (WMTS). Based upon information provided by the FCC, using the rule-of-thumb that SAR~P, for all P transferred into 1g then 1.6 mW/g requires 1.6mW, which is above the output of the device described in this certification application.

Exhibit Q: Technical Report-General Information FCC ID: CM676A91343-600 Measurement/Technical Report General Information Applicant: Spacelabs Medical Address: PO Box 97013 City, State, Zip Redmond, WA 98073-9713 Test Requested By: Steve Cantwell Model: 91347-05, 91343-05 FCC ID: CM676A91343-600 First Date of Test: June 10, 2002 Last Date of Test: June 17, 2002 Receipt Date of Samples: June 10, 2002 Job Number SPAC0307 Scope Regulatory Authority Federal Communications Commission Approval Type Certification Equipment Type Licensed Non-Broadcast Transmitter Worn on Body Rule Part 47CFR 95.1115 Rule Exemptions None Related Submittals or Grants None Report Information Prepared By Vicki Albertson, Technical Report and Documentation Manager Northwest EMC, Inc. Signature Issued By Northwest EMC, Inc. 22975 NW Evergreen Parkway, Suite 400 Hillsboro, Oregon 97124 Ph. (503) 844-4066 Fax (503) 844-3826 Report Number SPAC0307.1 Date Issued July 29, 2002 EUT Information Frequency Range 608-614 MHz Antenna Conducted Output Power .0008 EIRP Modulation FSK Antenna(s) Patch Antenna integral to the unit, not user-accessible Supply Power 9V DC Battery Test Facility The measurement facility used to collect the radiated and conducted data is located at Northwest EMC, Inc. 22975 NW Evergreen Parkway, Suite 400 Hillsboro, OR 97124 (503) 844-4066 Fax: 844-3826 This site has been fully described in a report filed with the FCC (Federal Communications Commission), and accepted by the FCC in a letter maintained in our files. Laboratory Accreditation Accreditation has been granted to Northwest EMC, Inc. to perform the Electromagnetic Compatibility (EMC) tests described in the Scope of Accreditation. Assessment performed to ISO/IEC 17025. Certificate Number: 1936-01, Certificate Number: 1936-02, Certificate Number 1936-03 FCC ID: CM676A91343-600 Exhibit A FCC ID Label and Location Exhibit B External Photos Exhibit C Internal Photos Exhibit D Schematics Exhibit E Frequency Block Diagram Exhibit F Tune-up Procedure Exhibit G User Manual 1 Exhibit H User Manual 2 Exhibit I Operational Description Exhibit J Request for Confidentiality Letter Exhibit K Agent Authorization Letter Exhibit L RF Exposure Exhibit M Spurious Radiated Emissions Exhibit N Field Strength of Fundamental Exhibit O Test Setup Photos Exhibit P Theory of Operations Exhibit Q Technical Report-General Information Exhibit R Justification for Emission Designator

Exhibit M: Spurious Radiated Emissions FCC ID: CM676A91343-600 Northwest EMC Spurious Radiated Emissions Revision 2/4/02 Spac0307 Justification The individuals and/or the organization requesting the test provided the modes, configurations and settings available to evaluate. While scanning the radiated emissions, all of the EUT parameters listed below were investigated. This includes, but may not be limited to, antennas, tuned transmit frequency ranges, operating modes, and data rates. Channels in Specified Band Investigated: High Low Operating Modes Investigated: Typical Antennas Investigated: Integral Data Rates Investigated: Maximum Output Power Setting(s) Investigated: Maximum Power Input Settings Investigated: Battery Frequency Range Investigated Start Frequency 30 MHz Stop Frequency 6.14GHz Software\Firmware Applied During Test Exercise software Standard Production Software Ve…

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