BQI02DT-7000PATIENTNET

PatientNet Operator’s Manual, 10001001-00X, Draft PATIENTNET  OPERATOR’S MANUAL Software Version 1.04 Operator’s Manual Part Number 10001001-00X, Draft PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft Note: Due to continuing product innovation, specifications in this manual are subject to change without notice. Copyright ©2001 GE Medical Systems Information Technologies. All rights reserved. 15222 Del Amo Avenue, Tustin, California 92780 Limited Software License and Equipment Use The PatientNet Suite of Products is covered under U.S. Patent numbers 5,944,659 and 5,748,103 and one or more pending patent applications. All software licensed by GE Medical Systems Information Technologies to Customers is licensed under a lim- ited, non-transferable license and reserves all rights not expressly granted. The soft- ware license permits the customer to use the software only on equipment purchased from the manufacturer. The customer may not copy, modify, loan, rent, lease or other- wise transfer the software or assign, transfer or sub-license the software to any other party without prior written consent, and any attempt to do so will render the software license null and void. The customer may not sublet the equipment sold to it and will not permit it to be used by anyone other than the customer’s qualified personnel. Modifica- tion or hooking up of other equipment to the supplied equipment, including software and related instruments cannot be made without GE Medical Systems Information Technologies written authorization. Manuals or other written documentation may not be copied or distributed without GE Medical Systems Information Technologies authorization. Listed below are GE Medical Systems Information Technologies Trademarks. All other trademarks contained herein are the property of their respective owners. Mobile-PatientViewer, OpenNet, PatientBrowser, SiteLink, PatientNet, and DINAMAP. Propaq and Encore are trademarks of Protocol Systems, Inc. Pass- port is a registered trademark of Datascope Corp. Microsoft, Windows, and Win- dows NT are registered trademarksof Microsoft Corporation in the United States of America and other countries. While we have endeavored to supply as complete and accurate a trademark list as pos- sible, the manufacturer makes no warranties, express or implied, as to the completeness and accuracy of this list. This list does not constitute an endorsement of any particular manufacturer. TECHNICAL SUPPORT INFORMATION PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft TECHNICAL SUPPORT INFORMATION PatientNet  Operator’s Manual Technical/Service/Clinical Support Our support professionals are ready to help you with operations and clinical applica- tion questions, parts replacement requests, supplies, technical and clinical training, or product service emergencies. We are available 24 hours a day, 7 days a week. Telephone 714.546.0147 800.955.2424 Continental United States Fax 714.571.4155 Customers with GE Medical Systems Information Technologies products under war- ranty, or with a current service agreement, receive 24-hours-a-day, 7-days-a-week support at no additional charge. Customers with GE Medical Systems Information Technologies products without a warranty, or without a current service agreement, receive support at no additional charge, Monday through Friday 8:00 a.m. to 5:00 p.m. PST, excluding holidays. After hours will be billed at current rates. To help us serve you better, please have the following information available when placing your call for support: •product name and serial number •software version •configuration information •problem description •your hospital’s address and telephone number TECHNICAL SUPPORT INFORMATION PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft Additional Resources Additional literature is available as shown below. To obtain copies, contact your sales representative. Contact the manufacturers of bedside monitors and ventilators used with PatientNet for literature on their equipment. part number PatientNet Administrator’s Guide, software v1.0310001003-003 PatientNet Service Manual, software v1.01 and above10001002-001 Central Station Quick Reference Card, v1.0X Series10001036-004 IRVS Quick Reference Card, v1.0X Series10001036-005 RVS Quick Reference Card, v1.0X Series10001036-006 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft v All information contained herein is subject to the rights and restrictions on the title page. TABLE OF CONTENTS Technical Support Information......................................................................................................... 3 PatientNet“ Operator’s Manual .................................................................................................... 3 List of Figures ................................................................................................................................... ix List of Tables................................................................................................................................... xiii Introduction ...................................................................................................................................... 15 Getting Started ............................................................................................................................ 15 About This Manual ..................................................................................................................... 16 Technical Support and Literature Resources .............................................................................. 16 Clinical Calculations................................................................................................................... 17 Clinical Use and Responsibility.................................................................................................. 18 Warnings, Cautions, and Notes ..........................................…

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ADMIT, DISCHARGE, AND PATIENT DEMOGRAPHIC INFORMATION PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft 73 All information contained herein is subject to the rights and restrictions on the title page. ADMIT, DISCHARGE, AND PATIENT DEMOGRAPHIC INFORMATION This chapter tells you how to admit and discharge patients to the PatientNet System and how to enter, view, modify and print patient demographic information. The settings described in this section are displayed on the Patient Settings screen (fig. 30). To display this screen, press Setup on the Main screen. Fig. 30. Patient Settings screen Admitting a Patient to the System Admit a patient at the Central Station as follows: 1. Select an available patient channel by clicking on the waveform area. The presence of the Admit button on the Patient Settings screen indicates that a channel is available. 2. Press the Admit button. 3. Enter demographic information and clinical setting for this patient as instructed in the following sections. If the transceiver is transmitting when you press Admit, the system verifies that the transceiver or device type matches the configuration for the channel. If the data does not match, the ?? SOURCE alarm is triggered. Note:The System Administrator may configure the system to make it mandatory to enter specific patient demographic data before admitting a patient. The required fields may include name, nursing unit, room number, physician, and ID number. ADMIT, DISCHARGE, AND PATIENT DEMOGRAPHIC INFORMATION 74 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft All information contained herein is subject to the rights and restrictions on the title page. Entering Patient Information Once a patient is admitted, press the Patient Data button to display the Patient Data Entry screen (fig. 31). Fig. 31. Patient Data Entry screen 1. Highlight Patient Name in the list of items. 2. Press the Keyboard button. 3. Using the on-screen keyboard, type in the patient’s name then press the Enter button. You can also enter information with the external keyboard. 4. Enter the additional demographic information for other items in the same way. Note:Notice that the patient’s name and ID number now appear on the waveform area. Available fields are shown below. The Number of Characters value is the maximum number allowed in each field. 5. Click the Pager # button to display the number pad and enter the pager num- ber that is assigned to the patient. If a pager is not assigned, then click N on the number pad to indicate None. 6. Click on the Display Wave button to toggle through the available waveforms for the selected patient. ADMIT, DISCHARGE, AND PATIENT DEMOGRAPHIC INFORMATION PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft 75 All information contained herein is subject to the rights and restrictions on the title page. 7. Click the size mm/mv button (this button varies depending on the device type) to select the size of the waveform that is displayed. 8. Click the Next button to select the Primary and Secondary leads for Arrhythmia analysis. Note:For best results, select lead II for your Primary Lead, and lead V or I for your Secondary Lead. Note:The Primary and Secondary Lead selection is a configurable option. See your system administrator if these buttons are inactive. Table 6. Patient information fields and character amounts. Viewing Patient Information 1. Press Patient Data on the Patient Settings screen (fig. 30). The View Data screen appears, showing the information entered when the patient was admit- ted along with the admit date and time and the time since admit. 2. Use the arrow buttons and PgUp and PgDn to scroll through the information fields. Patient Data FieldNumber of Characters Patient Name18 Room/Bed6 Nursing Unit18 Patient ID20 Date of Birth18 Sex (M/F)1 Physician18 Physician Group18 Diagnosis18 Orders18 Notes 118 Notes 218 Notes 318 Medication 118 Medication 218 Medication 318 ADMIT, DISCHARGE, AND PATIENT DEMOGRAPHIC INFORMATION 76 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft All information contained herein is subject to the rights and restrictions on the title page. Modifying Patient Information Modify existing patient demographic information on the View Data screen (fig. 32). Fig. 32. View Data screen 1. Press Patient Data on the Patient Settings screen. 2. Press Modify Data on the View Data screen to re-display the Patient Data entry screen. 3. Highlight the information field you wish to change and type in your changes for that field using either the on-screen keyboard or the external keyboard. 4. Press the Enter button on the keyboard. Note:If any of the demographic fields are set to Pre-Admit by the System Admin- istrator, then the appropriate demographic information must be entered before a patient may be admitted. If any of the demographic settings are set to Pre-Admit and you attempt to admit a patient without entering the proper information, then a popup will be displayed stating that the information must be entered prior to admitting the patient. ADMIT, DISCHARGE, AND PATIENT DEMOGRAPHIC INFORMATION PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft 77 All information contained herein is subject to the rights and restrictions on the title page. Printing Patient Information You may want to maintain a record of patient demographic information as contained in the PatientNet System. To do so, print the Patient Data Report (fig. 33) from the laser printer for the patient’s file. 1. Press Patient Data on the Patient Settings screen to display the Patient Data Entry screen (fig. 31) or the View Patient Data screen. 2. Press Laser to print the Patient Data Report. Fig. 33. Patient Data Report ADMIT, DISCHARGE, AND PATIENT DEMOGRAPHIC INFORMATION 78 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft All information contained herein is subject to the rights and restrictions on the title page. Discharging a Patient From the System Discharging a Patient at the Central …

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FULL DISCLOSURE PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft 151 All information contained herein is subject to the rights and restrictions on the title page. Displaying Data from a Specific Time You can display data taken at any time in the past 24/72 hours. If no trend data is available for the time you select, data closest to this time is displayed. 1. Press Skip To on the Disclosure screen to display the Skip To popup (fig. 73). Fig. 73. Skip To Popup 2. On the popup keypad, enter the desired time: use A/P to set a.m. or p.m. Note:If using a 24-hour time setup, you do not need to specify a.m. or p.m. You must, however, use the colon (:) to separate the hour and minutes in the Skip To popup. 3. Press Enter to execute the command or press Skip To a second time to cancel. Note:If using 72-Hour Full Disclosure, you will also be required to specify the date. Displaying Data from an Earlier or Later Time Use the arrow buttons–left for earlier and right for later–to move the displayed wave- form. Continuously pressing the left or right arrows will quickly scroll through the available full disclosure screens. FULL DISCLOSURE 152 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft All information contained herein is subject to the rights and restrictions on the title page. Displaying Vital Statistics Press the Vitals buttons to display the patient’s vital statistics, as well as the primary and secondary arrhythmia leads and rhythm indicator (page 70), from the first valid sample in the disclosure screen. Fig. 74. Full Disclosure Vitals Popup Viewing the Previous Alarm Press the Prev Alarm button to display the previous alarm. FULL DISCLOSURE PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft 153 All information contained herein is subject to the rights and restrictions on the title page. Storing a Disclosure Waveform Segment as a History Event To store a 20-second waveform segment in Full Disclosure as a history event: 1. Highlight a wave segment to store. If it is longer than 20 seconds, the center 20-second segment is stored. If the waveform is fully zoomed in, there is no need to highlight a segment. The 7 sec- onds of zoomed-in data is stored. 1. Press the Options button to display the Options Popup (fig. 75). Fig. 75. Full Disclosure Options Popup 2. Press Store Events in the popup. Full Disclosure stores are automatically set to Archive. FULL DISCLOSURE 154 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft All information contained herein is subject to the rights and restrictions on the title page. Printing Full Disclosure You can print disclosure reports in 1, 2, 4, 8, 12, or 16 hour report, 24/72-hour report, 24/72-hour summary report, zoomed-in report formats, and 24/72-hour quality reports. These reports may be annotated with alarm violations and beat annotations. Note:With the 72-Hour Full Disclosure option enabled, you can also print a 24, 48, and 72-hour report, summary, and quality reports. Note:On laser strips, the Heart Rate value represents the average of the 10, one second, Heart Rates that are stored for the 10 seconds of printed data. Each stored Heart Rate is the running 6 beat average from the Arrhythmia analy- sis. See “Arrhythmia Analysis” on page 51 for details on Arrhythmia pro- cessing. 1. Press Laser on the Full Disclosure screen to display the Print popup (fig. 76). Fig. 76. Full Disclosure Report Popup 2. Select the button corresponding to the type of report you wish to print. Note:You can only print hourly reports and summaries while in Zoomed-Out Full Disclosure mode. Zoomed-In Full Disclosure allows you to print the full dis- closure segment as it is displayed on the screen. FULL DISCLOSURE PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft 155 All information contained herein is subject to the rights and restrictions on the title page. One Hour Disclosure Report This report prints from 15 minutes to one hour of waveforms to a page, depending on the number of waves selected. •One waveform in the disclosure screen: one hour of data is printed on a page (one minute per line). •Two waveforms in the disclosure screen: 30 minutes of waveforms are printed on a page. •Three waveforms in the disclosure screen: 20 minutes of waveforms are printed on a page. •Four waveforms in the disclosure screen: 15 minutes of waveforms are printed on a page. The highest Priority alarm for each minute is printed to the right side. If alarms are turned off for the patient, the waveform is shaded in gray. Arrhythmia state is indicated by BED (bedside source), CEN (central source) and OFF. 2 hr report The 2 hour report prints the currently displayed hour and previous hour of disclosure data on multiple pages in the format defined above. 4 hr report The 4 hour report prints the currently displayed hour and previous 3 hours of disclo- sure data on multiple pages in the format defined above. 8 hr report The 8 hour report prints the currently displayed hour and previous 7 hours of disclo- sure data on multiple pages in the format defined above. 12 hr report The 12 hour report prints the currently displayed hour and previous 11 hours of disclo- sure data on multiple pages in the format defined above. 16 hr report The 16 hour report prints the currently displayed hour and previous 15 hours of disclo- sure data on multiple pages in the format defined above. Cancel Pressing the cancel button closes the print popup and no reports are printed. 24/72-Hour Disclosure Report This report is similar to the one hour report and is printed at the Central Station even if requested at a PatientNet Viewer (also known as an IRVS or RVS). FULL DISCLOSURE 156 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft All information contained herein is subject to the rights and restrictions on the title page. 24/72-Hour Summary Report This report prints summary graphs of all data trended during the last 24/72 hours and the total number of alarm violations. It leaves space for …

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TROUBLESHOOTING PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft 205 All information contained herein is subject to the rights and restrictions on the title page. TROUBLESHOOTING Arrhythmia Calls No matter how sophisticated an arrhythmia monitoring program may be, no real-time monitoring equipment recognizes the presence or absence of P-waves. Therefore, it is very important to remember that alarms will not sound for certain arrhythmias unless the heart rate exceeds the upper and lower limits for heart rate. Note:Close observation of the patient’s rhythm by a trained clinician is vital. Rhythms, such as Sinus Arrhythmia, will not be called. Sinus Bradycardia and Sinus Tachycardia will cause the system to alarm only if the rate exceeds the lower or upper alarm limits. First Degree AV block will not be detected; Second Degree AV Blocks will be alarmed if the rate violates the lower alarm limit. Complete Heart Block will signal an alarm event if it violates the lower alarm limit. The system will not call PACs, except only as aberrant beats. Paroxysmal Atrial Tachycardia (PAT) will trigger an alarm if the heart rate exceeds the upper alarm limit as “SV-TACH” if greater than 8 Supraventricular ectopic beats at 150 BPM. Atrial Fibrillation and Atrial Flutter will not alarm as a specific alarm, but alarm notification will occur if the rate violates the upper or lower alarm limits. AV Nodal/Junctional Rhythm/Tachycardia will be called if the rate exceeds the upper or lower alarm limits. The ventricular calls High PVC, Couplet, Trigeminy, Bigeminy, V-Rhythm, V-Run, and V-TACH will trigger alarm notification. V-Tach, V-Rhythm, and V-Run are called based on how the V-TACH alarm is configured. See “Configuring the V-TACH Alarm Limits” on page 115 for details. If you find that you are missing higher level ventricular alarms, then set the lower level alarms on Couplet, and adjust the high heart rate alarm notification lower in order to catch these events. TROUBLESHOOTING 206 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft All information contained herein is subject to the rights and restrictions on the title page. There are three general categories of questionable arrhythmia calls. 1.False Positive Calls result when the arrhythmia system signals an arrhythmia when there is none. It is important to understand how the algorithm analyzed the rhythm. 2.False Negative Calls result when the arrhythmia system fails to detect and signal an arrhythmia event when one is present. 3.Incorrect Analysis occurs when the system signals that an arrhythmia event occurred, but classifies it incorrectly. Note that it is important that the system alarmed and alerted the system operator to a change in the patient rhythm. If there are too many false positive calls, then the system operator may become desen- sitized to the alarms. That is why it is important that you understand what factors con- tribute to false positive calls and correct this situation when possible. TROUBLESHOOTING PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft 207 All information contained herein is subject to the rights and restrictions on the title page. Examples Many of the types of false positive calls are related to electrode application and signal quality. Let’s consider several examples. Example 1 - False High PVC Alarm Problem High PVC alarm occurs but no PVCs are present. Fig. 93. Example 1 - False Positive Call Correction •Press the Re-learn button to discard the patient’s previous templates and replace them with the current templates. •Check for dry electrodes. It may be time to replace them. •Least preferable, but still a possible solution: select a higher value for the PVC alarm or temporarily turn off the “High PVC” alarm. Example 2 - False Arrhythmia Alarm Problem Alarms are occurring, but no abnormal arrhythmias are present. The patient’s intrinsic QRS has a high degree of variability that is associated with the following: •Atrial Fibrillation/Flutter with aberrant conduction •Intermittent or sustained right or left bundle branch block •Cardiomyopathy TROUBLESHOOTING 208 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft All information contained herein is subject to the rights and restrictions on the title page. Fig. 94. Example 2 - False Positive Call Correction Persistent QRS variability in the patient’s dominant rhythm is a rather difficult prob- lem for computerized arrhythmia detection. Only the trained caregiver can judge if a specific QRS morphology represents a variation in the patient’s basic QRS or if it is abnormal. However, in an attempt to reduce the number of alarms, you can perform the following steps: 1. Turn off all nonessential alarms 2. Press the Re-learn button when the patient’s dominant QRS is stable TROUBLESHOOTING PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft 209 All information contained herein is subject to the rights and restrictions on the title page. Example 3 - Missed Ventricular Tachycardia Problem Sometimes the arrhythmia system calls a ventricular arrhythmia differently than the clinicians would. Remember that the system has criteria which must be met. For example, V-TACH is called when the rate is greater than or equal to 100 BPM and 3 consecutive PVCs are detected. If the ventricular abnormal varies, then the system may mis-classify some of the beats as non-ventricular. Fig. 95. Example 3 - Missed V-TACH Call Correction In these situations, the high heart rate limit may be decreased, which will provide alarm notification. Enabling a lower level ventricular alarm may provide a safety fac- tor for an alarm call, such as Couplet. This may be called before the system qualifies the rhythm as V-TACH and would provide proper alarm notification to obtain the attention of the system operator or caregiver. TROUBLESHOOTING 210 PatientNet Operator’s Manual, v1.04, 10001001-00X, Draft All information contained herein is subject to the rights and restrictions on the title pa…

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November 18, 2002 Technical Certification Body TUV America, Incorporated 10040 Mesa Rim Road San Diego, CA 92121 RE: Authorization & Anti-Drug Abuse Dear TCB: Data Critical Corporation, an operating entity of GE Medical Systems Information Technologies, hereby authorizes TUV America to act as our agent in all matters relating to the FCC application for equipment authorization for the DT-7000 and DT-7001. This authorization includes signing all documents relating to the FCC application. I further certify that the applicant nor any part to the application is subject to a denial of Federal benefits, that includes FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 USC Section 862. This authorization expires on 1 December 2003. Sincerely, Diana Thorson, RA Manager Phone: 714-247-4135 Fax: 714-571-3945 November 22, 2002 Technical Certification Body TUV America, Incorporated 10040 Mesa Rim Road San Diego, CA 92121 RE: Request for Confidentiality Dear TCB: Data Critical Corporation, an operating entity of GE Medical Systems Information Technologies, pursuant to Sections 0.457(d)(1)(ii) and 0.459 of the Commission’s Rules, hereby requests confidential treatment of information accompanying schematics, block diagrams, operational descriptions and the like, including but not necessarily limited to: Title Description DT-7001 Block Diag.doc block diagram of the EUT (digital and RF modules), (note that the “DM-8000” is the RF module) 12111111-102_4d Digital Schematic.pdf schematic of the digital board 12111111-000_6F Digital BOM.pdf bill of material for the digital board RF 608 revB Schematic.pdf schematic of the RF board RF 608 BOM 5-5-02.doc bill of material for the RF board RF Block Diag.doc block diagram of just the RF module Op Des & Design Info.doc detailed description of receive and transmit FHSS & TDMA Descr.doc detailed description of channel use (RF on-time) The above materials contain trade secrets and proprietary information not customarily released to the public. The public disclosure of these matters might be harmful to the Data Critical and provide unjustified benefits to our competitors. Data Critical understand that pursuant to Rule 0.457(d)(1)(ii), disclosure of this application and all accompanying documentation will not be made before the date of the Grant of this application. Sincerely, Diana Thorson, RA Manager Phone: 714-247-4135 Fax: 714-571-3945

Top with antenna Inside Top with out antenna Bottom and side

BOARD WITH ANTENNA OPPOSITE SIDE WITHOUT BATTERIES BOARD WITH BATTERIES

Package Frequency Range (fo) Mode of Operation o Calib. Tol. @ 25C Temp. Range Aging/Year (fa) F r e q u e n c y S t a b i l i t y T e m p . R a n g e C a p a c i - t a n c e Operating (TOPR) Storage (TSTG) Drive Level (DL) Load (CL) Equiv. Series Resist. (R) 1 Shunt (C) O CCM2 - Low-Profile Ceramic 3.500MHz~25.000MHz AT Fundamental ± 50ppm (std.); 30ppm (opt.) ± 50ppm (std.); 30ppm (opt.) st ± 5ppm (1 year std.) 18pF (std.); Specify if different 100μW (max.) Varies per frequency (see chart) 7pF (max.) Dimensions (mm) Recommended Pad (mm) SpecificationsActual Size Standard Options E.S.R. (Std. Max. Ratings) Features 3.5~3.99MHz AT-Cut Fund. 4.0~5.99MHz AT-Cut Fund. 6.0~9.99MHz AT-Cut Fund. 10.0~13.99MHz AT-Cut Fund. 14.0~25.0MHz AT-Cut Fund. 100Ω 80Ω 50Ω 150Ω 200Ω 5Heat-Resistant Ceramic Package 5Reliable AT-Fundamental Logic 5Low Profile Package 5Compact Package Size for High Density Applications 5Embossed Taping for Automated Placement oooo -10C~60C (std.); -40C~85C (opt.) oo -55C~125C (std.) 5 . 5 ± 0 . 5 2 . 0 ± 0 . 2 2 . 5 1 . 5 1 . 5 ± 11.6 0.2 5.08 3.082.02.0 S ## Series Specify Load Cap. (pF) other than 18pF C9 C10 SC ± 30/30ppm ± 30/50ppm Custom Stab. R6 oo -40~85C TOPR 2 . 3 2 . 3 1 . 1 2.68 2.4 2.4 CCM2 Low Profile Ceramic uuu 22600-C Lambert Street, Suite 903 Lake Forest, CA 92630 Tel: (949) 588-2800 Fax: (949) 588-2810 Surface Mount Crystal SPECIFICATIONS ARE SUBJECT TO CHANGE WITHOUT NOTICE. PLEASE CONTACT YOUR IMPACT SALES REPRESENTATIVE FOR CUSTOM SPECIFICATIONS, CURRENT INFORMATION, PRICING AND AVAILABILITY. D-6 IMPACT, LLC

TÜV AMERICA, INC. 10040 Mesa Rim Road San Diego, CA 92121-2912 Phone 858 546 3999 FAX 858 546 0364 Report No. SC205752-03 Page 1 of 19 Rev.No 1.0 MEASUREMENT AND TECHNICAL REPORT GE MEDICAL SYSTEMS - IT 15222 del Amo Avenue Tustin, CA 92780 DATE: 25 November 2002 This Report Concerns: Original Grant: X Class II Change: Equipment Type: DT-7001 Instrument Transceiver, Model DT-7001* (*) Model numbers represent per customer: DT-7000 and DT-7001. DT-7001 deemed worst case. Deferred grant requested per 47 CFR 0.457(d)(1)(ii)? Yes: Defer until: No: X Company Name agrees to notify the Commission by: N/A of the intended date of announcement of the product so that the grant can be issued on that date. Transition Rules Request per 15.37? Yes: No: X* (*) FCC Parts 2 and 95, Paragraph(s) 2.1049, 2.1055 and 95.1115(a), 95.1115(b), 95.1115(e) Report Prepared by: TÜV AMERICA, INC 10040 Mesa Rim Road San Diego, CA 92121-2912 Phone: 858 546 3999 Fax: 858 546 0364 TÜV AMERICA, INC. 10040 Mesa Rim Road San Diego, CA 92121-2912 Phone 858 546 3999 FAX 858 546 0364 Report No. SC205752-03 Page 2 of 19 Rev.No 1.0 TABLE OF CONTENTS Pages 1.0 GENERAL INFORMATION 3 - 8 1.1 Product Description 3 - 6 1.2 Related Submittal Grant 7 1.3 Tested System Details 7 1.4 Test Methodology 7 1.5 Test Facility 7 1.6 Part 2 Requirements 8 2.0 SYSTEM TEST CONFIGURATION 9 2.1 Justification 9 2.2 EUT Exercise Software 9 2.3 Special Accessories 9 2.4 Equipment Modifications 9 2.5 Configuration of Test System 9 3.0 FIELD STRENGTH OF FUNDAMENTAL EQUIPMENT/DATA FIELD STRENGTH OF OUT OF BAND EMISSIONS EQUIPMENT/DATA FREQUENCY STABILITY VS VOLTAGE EQUIPMENT/DATA OCCUPIED BANDWIDTH 10 - 18 4.0 ATTESTATION STATEMENT 19 TÜV AMERICA, INC. 10040 Mesa Rim Road San Diego, CA 92121-2912 Phone 858 546 3999 FAX 858 546 0364 Report No. SC205752-03 Page 3 of 19 Rev.No 1.0 1.0 GENERAL INFORMATION 1.1 Product De…

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