U6VCBSENCCardio Sen`C

User Manual (DRAFT) July 2007 CardioSen’C __________________________________________________________________________________________________ Medical call center telephone number: 800 227 3462 2 In case of any doubts or questions regarding the use of this device, do not hesitate to call our medical call center for support: 800 227 3462 _______________________ Note We strongly recommend that you read this manual carefully and in its entirety before using the device for transmission. A thorough understanding of the operation and use of the CardioSen’C is required for correct and accurate ECG transmission. This telephone number can be found at the bottom of each page Please fill in the telephone number and details of your personal physician in the space provided below: CardioSen’C __________________________________________________________________________________________________ Medical call center telephone number: 800 227 3462 3 Table of Contents 1. Conditions for use 4 2. Indications for use 4 3. Device Description 5 4. Setting up the CardioSen’C 7 5. ECG transmission 9 6. Maintenance information 16 7. Equipment classification 18 8. Operating and storage conditions 20 9. Technical specifications 20 10. Limited warranty 21 CardioSen’C __________________________________________________________________________________________________ Medical call center telephone number: 800 227 3462 4 1. Conditions for use Individuals unable to perform ALL of the following tasks should refrain from using the CardioSen’C: • Operate a hand-held telephone • Read and understand the user manual • Place the CardioSen’C against the chest, holding it steadily in place for up to thirty seconds using your left hand • Operate a simple, push-button device • Operate the device while sitting Caution for carriers of pacemakers or internal cardiac defibrillators The CardioSen’C’s cover door contains an antenna and cellular modem for transmitting data through the cellular telephone network. To avoid any potential interference when measuring an ECG, users with pacemakers or internal cardiac defibrillators should maintain a minimum of 6 inches (15 centimeters) between the CardioSen’C’s open cover door and their implanted device. 2. Indications for use The CardioSen’C device is intended to condition an electrocardiographic signal so that it can be transmitted digitally over the cellular network or acoustically via telephone to a remote location. The CardioSen’C device is designed to be used by a patient to transmit a 12-lead ECG and rhythm strip in real-time to a physician’s office, hospital or other medical receiving center. Caution ƒ The use of the device should always be in conjunction with a medical center capable of receiving the ECG ƒ The purchase of this device should not substitute for care recommended by your family physician or cardiologist CardioSen’C __________________________________________________________________________________________________ Medical call center telephone number: 800 227 3462 5 3. Device Description The CardioSen’C enables an individual to transmit a 12-lead ECG to a physician's office, hospital or monitoring center. It transmits the ECG measurement via two distinct channels: acoustic and digital. The acoustic transmission uses a standard telephone to transmit acoustically coupled tones produced by the CardioSen’C housing device. These are sent out to healthcare professionals, who are able to convert the tones to a standard 12-lead ECG and interpret the results, providing rapid diagnosis of the user’s condition. In addition, the ECG measurement is transmitted digitally by means of a built-in modem via a cellular telephone network. As with the acoustic method the measurement is relayed to qualified healthcare professionals to interpret the data. The total duration of a full 12-lead ECG transmission is roughly twenty-three seconds. The following diagrams are of the device, its components and related accessories. Diagram 1: The CardioSen’C with component identification 3. Electrode belt 1. Housing 10. Operating button 9. Speaker for acoustic transmission 6. Chest size numbering indication 4. Gender selection switch 7. Square black (waist) electrode 8. Round grey (right arm) electrode 2. Display 13. Infra red sensor 5. Cover doo r 11. Elastic band 12. Elastic band buckle CardioSen’C __________________________________________________________________________________________________ Medical call center telephone number: 800 227 3462 6 1. Housing is placed against the center of the bare chest for electrocardiogram signal detection and contains the necessary electronics and battery. 2. LCD display indicates network reception, battery level, gender selection and size (see Diagram 2 below for detailed description). 3. Electrode belt wraps around the left side of the chest for electrocardiogram signal detection. 4. Gender selection switch changes the device for either male or female users. 5. Cover door activates and deactivates the device and contains the cellular modem and antenna. 6. Chest size numbering indication used for determining the proper chest size setting. 7. Square black (waist) electrode is placed at the belt line against the bare skin, halfway from the navel to the left hip for electrocardiogram signal detection. 8. Round grey (right arm) electrode is placed under right underarm for electrocardiogram signal detection. 9. Speaker for acoustic transmission emits series of tones for the acoustic transmission of the ECG measurement. 10. Operating button initiates the ECG transmission. 11. Elastic band wraps around the right side of the chest and back in order to keep the housing and electrode belt in place. 12. Elastic band buckle adjusts the length of the elastic band and clasps onto the housing device. 13. Infrared sensor for maintenances by an authorized technician only. Diagram 2: Housing LCD display 1. Network reception level indicator shows the level of the cellular network reception for …

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attn: Reviewing Engineer MET Laboratories, Inc. 914 West Patapsco Avenue Baltimore, MD 21230 RE: 15.19 Statement (FCC ID: U6VCBSENC) TO WHOM IT MAY CONCERN The statement: "This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation” Is not placed in the label of the equipment due to the following reasons: - Type label is too small (No room for this writing). - Required text is already included in the user guide This statement is placed in a prominent location in the instruction manual. Please contact me if there is any information you may need. If you have any questions, please feel free to contact me at the address shown below. Sincerely, P.A. Name/Title: Mr. Roni Kazaz / Products Development Director Company name: SHL Telemedicine International Ltd. Telephone: +972-3-5612212 E-mail Address: [email protected]

attn: Reviewing Engineer MET Laboratories, Inc. 914 West Patapsco Avenue Baltimore, MD 21230 RE: CONFIDENTIALITY REQUEST FOR D301 (FCC ID: U6VCBSENC) To Whom It May Concern: Pursuant to Paragraphs §0.457 and 0.459 of the Commission’s Rules (47 C.F.R.) and Section §552(b) (4) of the Freedom of Information Act, SHL Telemedicine International Ltd. requests confidentiality for the following products: FCC ID Model U6VCBSENC Cardio Sen`C For the product stated above, we request that the following information be held confidential: 1) Circuit diagrams 2) Block Diagrams 3) Bill of materials 4) Operational Description 5) Power tune-up procedure No other items submitted as part of the equipment authorization filing process are deemed confidential. The above exhibits contain SHL Telemedicine International Ltd. trade secrets and proprietary information that could be of benefit to our competitors. This material is not customarily available to the general public and we request that it be withheld from public inspection. Please contact me if there is any information you may need. Sincerely, P.A. Name/Title: Mr. Roni Kazaz / Products Development Director Company name: SHL Telemedicine International Ltd. Telephone: +972-3-5612212 E-mail Address: [email protected]

Jennifer Sanchez From: Domingo Jiménez Barranco [[email protected]] Sent: Thursday, September 06, 2007 1:05 PM To: Jennifer Sanchez; [email protected] Cc: Cheryl Anicete; Liming Xu; Tony Permsombut; Jenn Warnell; Samantha Sharbonda; Kevin Mehaffey Subject: RE: U6VCBSENC/Cardio Sen`C/Par3 of 3 Attachments: 75900645 Report 02 Issue 3.pdf 9/6/2007 Hi Jennifer, I am writing you on behalf of my colleague Ricardo Orejas regarding this project (CardioSen’C, FCC ID: U6VCBSENC) Please find attached requested modified test report as requested by technical reviewer (please check email below of 6 th August). I hope it meets your requirements and we can close this FCC approval ASAP. I am sorry about the delay in getting this report fixed to you, due to our vacations period... Please keep us updated about when the FCC grant will be issued, as I need to inform the customer. Thanks Best regards Domingo De: Jennifer Sanchez [mailto:[email protected]] Enviado el: lunes, 06 de agosto de 2007 23:01 Para: Ricardo Orejas Rodríguez CC: Cheryl Anicete; Liming Xu; Oscar Castañeda Aguadero; Tony Permsombut; Jennifer Sanchez; Jennifer Warnell; Sara González López; Samantha Sharbonda; Kevin Mehaffey Asunto: RE: U6VCBSENC/Cardio Sen`C/Par3 of 3 Hi Sara, Our technical reviewer has the following concerns: Please provide RF power levels as measured values (Not 33dBm x 2 or 30dBm x 2) for all setup plots in SAR test report (Please refer RF test report). Please provide as soon as possible. If you have any questions, please let me know. Thanks! Jennifer Jennifer Sanchez TCB Administrator/Technical Writer MET Laboratories, Santa Clara CA 408-213-2359 Cell: 408-829-1603 www.metlabs.com







 


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TECHNICAL MANUAL Telit GE863-QUAD/PY Quad Band GPRS Data Terminal Module Pag.64 of 68 Rev. 0 8.2 Photos of CS1186a-A PCB primary layer TECHNICAL MANUAL Telit GE863-QUAD/PY Quad Band GPRS Data Terminal Module Pag.65 of 68 Rev. 0 8.3 Photos of CS1186a-A PCB secondary layer

REPORT ON Specific Absorption Rate Testing of the SHL Telemedicine International Ltd Cardio Sen’C ECG Cardiograph (Recorder/Transmitter) FCC ID: U6VCBSENC Doc Number 75900645 Report 02 Issue 3 September 2007 Choose certainty. Add value. TUV Product Service Ltd, Octagon House, Concorde Way, Segensworth North, Fareham, Hampshire, United Kingdom, PO15 5RL Tel: +44 (0) 1489 558100. Website: www.tuvps.co.uk ; www.babt.com Doc Number 75900645 Report 02 Issue 3 Page 1 of 29 REPORT ON Specific Absorption Rate Testing of the SHL Telemedicine International Ltd Cardio Sen’C ECG Cardiograph (Recorder/Transmitter) Doc Number 75900645 Report 02 Issue 3 FCC ID U6VCBSENC PREPARED FOR SHL Telemedicine Global Trading Ltd Wil House Shannon Business Park Shannon CO. Clare Ireland. ATTESTATION The wireless portable device described within this report has been shown to be capable of compliance for localised specific absorption rate (SAR) for General Population/Uncontrolled Exposure Limits as defined in the FCC standard Supplement C (Edition 01-01) to OET Bulletin 65 (Edition 97- 01) of 1.6 W/kg. The measurements shown in this report were made in accordance with the procedures specified in Supplement C (Edition 01-01) to OET Bulletin 65 (Edition 97-01) and IEEE 1528-2003 All reported testing was carried out on a sample of equipment to demonstrate compliance with the above standards. The sample tested was found to comply with the requirements in the applied rules. PREPARED BY V Kerai Telecoms Engineer APPROVED BY M Jenkins Authorised Signatory DATED 6 th September 2007 Note: The test results reported herein relate only to the item tested as identified above and on the Status Page. This report has been up-issued to include Input Power Level Values Obtained From CETECOM Report No.: 22345RET, Dated 2005-11-29 and Annex B – Additional Information Regarding the Integration Module. FCC ID: U6VCBSENC Doc Number 75900645 Report 02 Issue 3 Page 2 of 29 CONTENTS Section Page No 1 REPORT SUMMARY 1.1 Status .............................................................................................................................. 4 1.2 Summary .......................................................................................................................... 5 1.3 Test Results Summary ..................................................................................................... 6 2 TEST DETAILS 2.1 SAR Measurement System .............................................................................................. 8 2.1.1 Robot System Specification 2.1.2 Probe and Amplifier Specification 2.1.3 SAR Measurement Procedure 2.2 850MHz GPRS Body SAR Distributions (Area Scans – 2D).......................................... 13 2.3 1900MHz GPRS Body SAR Distributions (Area Scans – 2D)........................................ 16 3 TEST EQUIPMENT 3.1 Test Equipment .............................................................................................................. 20 3.2 Test Software ................................................................................................................. 20 3.3 Dielectric Properties of Simulant Liquids........................................................................ 21 3.4 Test Conditions............................................................................................................... 22 3.5 Measurement Uncertainty .............................................................................................. 23 4 PHOTOGRAPHS 4.1 Test Positional Photographs........................................................................................... 25 4.2 Photographs of Equipment Under Test (EUT)... ............................................................ 26 5 ACCREDITATION, DISCLAIMERS AND COPYRIGHT 5.1 Accreditation, Disclaimers and Copyright....................................................................... 29 ANNEX A Probe Calibration Information........................................................................................ A.2 ANNEX B Additional Information Regarding the Integration Module ............................................. B.2 FCC ID: U6VCBSENC Doc Number 75900645 Report 02 Issue 3 Page 3 of 29 SECTION 1 REPORT SUMMARY Specific Absorption Rate Testing of the SHL Telemedicine International Ltd Cardio Sen’C ECG Cardiograph (Recorder/Transmitter) Max 1g SAR (W/kg) 0.127 The maximum 1g volume averaged SAR level measured for all the tests performed did not exceed the limits for General Population/Uncontrolled Exposure (W/kg) Partial Body of 1.6 W/kg. Level defined in Supplement C (Edition 01-01) to OET Bulletin 65 (97-01). FCC ID: U6VCBSENC Doc Number 75900645 Report 02 Issue 3 Page 4 of 29 1.1 STATUS MANUFACTURING DESCRIPTION ECG Cardiograph (Recorder/Transmitter) STATUS OF TEST Specific Absorption Rate Testing POWER CLASS GSM 850 Class 4 / GSM 900 Class 4 GSM DCS 1800 / PCS 1900 Class 1 GPRS CLASS Class B GPRS MULTI-SLOT CLASS 10 (4Dn; 2Up; Sum5) MANUFACTURER SHL Telemedicine International Ltd TYPE OR MODEL NUMBER Cardio Sen’C HARDWARE VERSION V2.0 FIRMWARE VERSION V2.0 FCC ID U6VCBSENC SERIAL NUMBER 08001060 IMEI NUMBER 3582830011743501 BATTERY MODEL Energizer AA 2 Lithium - 3Vdc - 1.5Vx2 - max 0.6A BATTERY MANUFACTURER Eveready Battery Company TEST SPECIFICATIONS: 1. Federal Communications Commission (FCC) OET Bulletin 65c, Edition 01-01, Evaluating Compliance with FCC Guidelines for Human Exposure to Radiofrequency Electromagnetic Fields – Additional Information for Evaluating Compliance of Mobile and Portable Devices with FCC Limits for Human Exposure to Radiofrequency Emissions. REFERENCES: 2. US Federal Government, Code of Federal Regulations, Title 47 Telecommunication, Chapter I Federal Communications Commission, part 2, section 1093. 3. IEEE 1528 – 2003: Recommended Practice for Determining the Peak Spatial-Average Specific Absorption Rate (SAR) in the Human Body Due to Wireless Communications Devices: Experimen…

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Report No.: 25762RET Date: 2007-04-24 Page: 2 of 7 FDT08_04 INDEX 1. COMPETENCE AND GUARANTEES..........................................................................................3 2. GENERAL CONDITIONS..............................................................................................................3 3. CHARACTERISTICS OF THE TEST............................................................................................3 3.1 TEST REQUESTED.................................................................................................................3 3.2 REQUIREMENTS AND METHOD........................................................................................3 4. IDENTIFICATION DATA SUPPLIED BY THE APPLICANT.....................................................4 4.1 APPLICANT.............................................................................................................................4 4.2 REPRESENTATIVE................................................................................................................4 4.3 TEST SAMPLES SUPPLIER...................................................................................................5 4.4 IDENTIFICATION OF ITEM/ITEMS TESTED.....................................................................5 5. USAGE OF SAMPLES, PERIOD OF TESTING AND ENVIRONMENTAL CONDITIONS.....5 5.1 USAGE OF SAMPLES............................................................................................................5 5.2 PERIOD OF TESTING............................................................................................................5 5.3 ENVIROMENTAL CONDITIONS..........................................................................................6 6. TEST RESULTS..............................................................................................................................7 7. REMARKS AND COMMENTS......................................................................................................7 8. SUMMARY......................................................................................................................................7 ANNEXES ANNEX A. TEST RESULTS FOR FCC PART 22 ANNEX B. TEST RESULTS FOR FCC PART 24 ANNEX C. PHOTOGRAPHS Report No.: 25762RET Date: 2007-04-24 Page: 3 of 7 FDT08_04 1. COMPETENCE AND GUARANTEES Centro de Tecnología de las Comunicaciones (AT4 WIRELESS), S.A. is a laboratory with a measurement facility in compliance with the requirements of Section 2.948 of the FCC rules and has been added to the list of facilities whose measurements data will be accepted in conjunction with applications for Certification under Parts 15 or 18 of the Commission's Rules. Registration Number: 905266. In order to assure the traceability to other national and international laboratories, AT4 WIRELESS has a calibration and maintenance programme for its measuring equipment. AT4 WIRELESS guarantees the reliability of the data presented in this report, which is the result of measurements and tests performed to the item under test on the date and under the conditions stated on the report and is based on the knowledge and technical facilities available at AT4 WIRELESS at the time of execution of the test. AT4 WIRELESS is liable to the client for the maintenance by its personnel of the confidentiality of all information related to the item under test and the results of the test. 2. GENERAL CONDITIONS 1. This report only refers to the item that has undergone the test. 2. This report does not constitute or imply by its own an approval of the product by the Certification Bodies or competent Authorities. 3. This document is only valid if complete; no partial reproduction can be made without written approval of AT4 WIRELESS. 4. This test report cannot be used partially or in full for publicity and/or promotional purposes without previous written approval of AT4 WIRELESS and the Accreditation Bodies. 3. CHARACTERISTICS OF THE TEST 3.1 TEST REQUESTED 1. Measurements for PCS 850 and PCS 1900 devices according to FCC parts 22 and 24: -Radiated RF output power. -Radiated emissions. 3.2 REQUIREMENTS AND METHOD The test has been carried out according to the following documents and standards: 1. FCC part 22. 2. FCC part 24. Radiated testing was performed in AT4 WIRELESS' semi-anechoic chamber. This site has been fully described in a report submitted to the FCC and was accepted in a letter dated July 25, 2002. Radiated measurements were made in accordance with the general procedures of ANSI C63.4: 2003 and substitution method according to TIA/EIA 603-C: 2004. Report No.: 25762RET Date: 2007-04-24 Page: 4 of 7 FDT08_04 Uncertainty (factor k=2) was calculated according to the following AT4 WIRELESS' internal documents: 1. PODT000: Procedimiento para el cálculo de incertidumbres de medida The instrumentation used to perform the testing is listed below: 1. Semianechoic Absorber Lined Chamber IR 11. BS. 2. Control Chamber IR 12.BC. 3. Spectrum Analyzer Agilent E4440A. 4. Bilog antenna CHASE CBL6111. 5. Antenna tripod EMCO 11968C. 6. Antenna mast EM 1072 NMT. 7. Rotating table EM 1084-4. ON. 8. Double-ridge Guide Horn antenna 1-18 GHz HP 11966E. 9. Double-ridge Guide Horn antenna 18-40 GHz Agilent 119665J. 10. RF pre-amplifier Miteq AFS5-04001300-15-10P-6. 11. RF pre-amplifier Miteq JS4-12002600-30-5A. 12. EMI Test Receiver R&S ESIB26. 13. Universal Radio communication Tester R&S CMU200. 14. 10 dB attenuator HP 8491B. 15. Multi Device Controller EMCO 2090. 16. DC Power supply R & S NGPE 40/40. 4. IDENTIFICATION DATA SUPPLIED BY THE APPLICANT Identification data in this section has been supplied by the client. 4.1 APPLICANT Name or Company: SHL Telemedicine International Ltd. V.A.T.: ---- Address: Ashdar Building, 90 Igal Alon St. City: Tel Aviv Postal code: 67891 Country: ISRAEL Telephone: +972-3-5612212 Fax: +972-3-6242414 4.2 REPRESENTATIVE Name: Roni Kazaz (Products Development Director) Report No.: 2576…

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Report No.: 22345RET Date: 2005-11-29 Page: 2 of 10 FDT08_04 INDEX 1. COMPETENCE AND GUARANTEES..........................................................................................3 2. GENERAL CONDITIONS..............................................................................................................3 3. CHARACTERISTICS OF THE TEST............................................................................................3 3.1 TEST REQUESTED.................................................................................................................3 3.2 REQUIREMENTS AND METHOD........................................................................................4 4. IDENTIFICATION DATA SUPPLIED BY THE APPLICANT.....................................................5 4.1 APPLICANT.............................................................................................................................5 4.2 REPRESENTATIVE................................................................................................................5 4.3 TEST SAMPLES SUPPLIER...................................................................................................5 4.4 IDENTIFICATION OF ITEM/ITEMS TESTED.....................................................................6 5. USAGE OF SAMPLES, PERIOD OF TESTING AND ENVIRONMENTAL CONDITIONS.....6 5.1 USAGE OF SAMPLES............................................................................................................6 5.2 PERIOD OF TESTING............................................................................................................7 5.3 ENVIROMENTAL CONDITIONS..........................................................................................7 6. TEST RESULTS..............................................................................................................................9 7. REMARKS AND COMMENTS......................................................................................................9 8. SUMMARY....................................................................................................................................10 ANNEXES ANNEX A. TEST RESULTS FOR FCC PART 22 ANNEX B. TEST RESULTS FOR FCC PART 24 ANNEX C. MEASURING RESULTS FOR ELECTROMAGNETIC EMISSION ANNEX D. PHOTOGRAPHS Report No.: 22345RET Date: 2005-11-29 Page: 3 of 10 FDT08_04 1. COMPETENCE AND GUARANTEES Centro de Tecnología de las Comunicaciones (CETECOM), S.A. is a laboratory with a measurement facility in compliance with the requirements of Section 2.948 of the FCC rules and has been added to the list of facilities whose measurements data will be accepted in conjunction with applications for Certification under Parts 15 or 18 of the Commission's Rules. Registration Number: 905266. Centro de Tecnología de las Comunicaciones (CETECOM), S.A. is a laboratory with a measurement site in compliance with the requirements of RSS 212, Issue 1 (Provisional) and has been added to the list of filed sites of the Canadian Certification and Engineering Bureau. Reference File Number: IC 4621. In order to assure the traceability to other national and international laboratories, CETECOM has a calibration and maintenance programme for its measuring equipment. CETECOM guarantees the reliability of the data presented in this report, which is the result of measurements and tests performed to the item under test on the date and under the conditions stated on the report and is based on the knowledge and technical facilities available at CETECOM at the time of execution of the test. CETECOM is liable to the client for the maintenance by its personnel of the confidentiality of all information related to the item under test and the results of the test. 2. GENERAL CONDITIONS 1. This report only refers to the item that has undergone the test. 2. This report does not constitute or imply by its own an approval of the product by the Certification Bodies or competent Authorities. 3. This document is only valid if complete; no partial reproduction can be made without written approval of CETECOM. 4. This test report cannot be used partially or in full for publicity and/or promotional purposes without previous written approval of CETECOM and the Accreditation Bodies. 3. CHARACTERISTICS OF THE TEST 3.1 TEST REQUESTED 1. Measurements for PCS 850 and PCS 1900 device according to FCC parts 22 and 24 2. Continuous conducted emission, power leads: Standard: FCC Rules and Regulations 47 CFR Part 15 Limit: Class B Method: FCC Rules and Regulations 47 CFR Part 15, Subpart B y C 3. Radiated emission, electromagnetic field: Standard: FCC Rules and Regulations 47 CFR Part 15 Limit: Class B Method: FCC Rules and Regulations 47 CFR Part 15, Subpart B Report No.: 22345RET Date: 2005-11-29 Page: 4 of 10 FDT08_04 3.2 REQUIREMENTS AND METHOD The test has been carried out according to the following documents and standards: 1. FCC part 22. 2. FCC part 24. 3. FCC Rules and Regulations 47 CFR Part 15, Subpart B: Limits and methods of measurements for radio frequency devices. Unintentional radiators. 4. FCC Rules and Regulations 47 CFR Part 15, Subpart C: Limits and methods of measurements for radio frequency devices. Intentional radiators. Radiated testing was performed in Cetecom's semi-anechoic chamber. This site has been fully described in a report submitted to the FCC and was accepted in a letter dated July 25, 2002. Radiated measurements were made in accordance with the general procedures of ANSI C63.4 and substitution method according to TIA/EIA 603. The testing procedures used are: 1. PEEM001: Medida de la tensión perturbadora en bornes de alimentación según EN 55022. 2. PEEM002: Medida del campo perturbador radiado según EN 55022. Uncertainty (factor k=2) was calculated according to the following CETECOM's internal documents: 1. PODT000: Procedimiento para el cálculo de incertidumbres de medida 2. FEM12_07: Formato de cálculo de incertidumbre a aplicar en l…

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Report No.: 22345RET Date: 2005-11-29 Page: 1 of 6 Annex D FET18_00.DOC ANNEX D PHOTOGRAPHS (Number of photographs: 5) Report No.: 22345RET Report No.: 22345RET Date: 2005-11-29 Page: 2 of 6 Annex D FET18_00.DOC 1. Equipment with evaluation board. Report No.: 22345RET Date: 2005-11-29 Page: 3 of 6 Annex D FET18_00.DOC 2. Equipment with removed evaluation board Report No.: 22345RET Date: 2005-11-29 Page: 4 of 6 Annex D FET18_00.DOC 3. General test set-up for radiated measurements. Report No.: 22345RET Date: 2005-11-29 Page: 5 of 6 Annex D FET18_00.DOC 4. Test set-up for radiated measurements below 1 GHz. Report No.: 22345RET Date: 2005-11-29 Page: 6 of 6 Annex D FET18_00.DOC 5. Test set-up for radiated measurements above 1 GHz.

Report No.: 25762RET Date: 2007-04-24 Page: 2 of 6 Annex C FET18_00.DOC 1. Equipment (front view) Report No.: 25762RET Date: 2007-04-24 Page: 3 of 6 Annex C FET18_00.DOC 2. Equipment (back view) Report No.: 25762RET Date: 2007-04-24 Page: 4 of 6 Annex C FET18_00.DOC 3. General test set-up for radiated measurements. Report No.: 25762RET Date: 2007-04-24 Page: 5 of 6 Annex C FET18_00.DOC 4. Test set-up for radiated measurements below 1 GHz. Report No.: 25762RET Date: 2007-04-24 Page: 6 of 6 Annex C FET18_00.DOC 5. Test set-up for radiated measurements above 1 GHz.