TV9-MICLM-C001Wrist Worn Personal Location Device

Table of Content ColumbaTD – Utilization Guide 1. Device components 2. Subscription and activation of the ColumbaTD ser vice 3. Installation of the ColumbaTD system 3.1. Choice and installation of the bracelet 3.2. Installation of the charger and load of the Ba ttery- block 3.2.1. Installation and positioning of the charger 3.2.2. Load of the Battery-block 3.3. Load of the ColumbaTD 4. Operating modes 4.1. RF mode 4.2. Regular mode 4.3. Leaving secured zone mode 4.4. Emergency mode 5. Utilization of the ColumbaTD 5.1. Geo-localization 5.1.1. Leaving secured zone 5.1.2. Localize the ColumbaTD 5.2. In case of Emergency – alert button 5.3. Hands free telephony 5.3.1. Functioning 5.3.2. Contact the ColumbaTD wearer 5.4. Automated alerts 5.4.1. Low battery 5.4.2. Leaving protected zone 6. Conditions and usage environment 6.1. General instruction 6.2. Wet environment 6.3. Particular conditions 6.3.1. Pacemaker 6.3.2. Acoustic apparatuses 6.3.3. Medical apparatuses 6.3.4. Security onboard a plane 6.3.5. Magnetism 7. Internet website www.medicalmobile.com 8. After-sales service 9. Recycling of the ColumbaTD and its components 10. Specifications 10.1. Specifications 10.2. Network services 10.3. Positioning services 10.4. GPS positioning service 10.5. Autonomy 10.5.1. RF mode autonomy 10.5.2. Regular mode autonomy 10.5.3. Leaving protected zone mode autonomy 10.6. Data related to the specific absorption rate 11. Legal advice 11.1. Intellectual ownership 11.1.1. Patents and Copyrights 11.1.2. Trademark 11.2. FCC Statement 11.3. Conformity declaration – CE marking 11.4. Limited warranty 11.5. About this utilization guide Utilization Guide In order to assure the optimal functioning of the C olumbaTD system, entire reading of this guide must be completed prior usage. The reading of this guide must be completed with th e reading of the General Condition and Subscription Formulary of the ColumbaTD service, include in the box containing th e ColumbaTD system, which also contains important d ocuments and legal advices that must be understood and accepted before activating the ColumbaTD. 1. System Components A. Electrical plug allowing recharge with the Batte ry-block B. Speaker/ Microphone. C. Luminous signs: a. Blue: its regular flashes indicates that the Col umbaTD is functioning b. Red: Its flashes indicate low level of the batte ry and that a recharge is necessary. The red light constantly remains lit when the alert button is act ivated or if the ColumbaTD tries to establish a dis tant contact with informatics server. D. Alert Button. E. Notch allowing to maintain the Battery-block in place on the ColumbaTD during recharge F. Bracelets. G. Lock: the unbolting key must be inserted in the appropriate hole to unbolt the lock. 1. System Components Charger A. Electrical plug allowing reloading the Battery-b lock. B. Battery-block base. B. Notch allowing to maintain the Battery-block in place on charger’s base. D. Luminous signs: a. Red: Indicates that the battery block is chargin g. The light goes off when the charge is completed. b. Blue: Indicates that the charger is functional. E. Plug for the electrical supply wire. F. Base for the unbolting key. G. Radio antenna (RF). Battery-block A. Lock: Drive in the mechanism to maintain the ba ttery-block on the charger or on the ColumbaTD. B. Holes to insert the unbolting key to liberate th e battery-block of the charger’s notch or of the Co lumbaTD. C. Luminous signs: a. Yellow: Indicates the ColumbaTD is charging. The light goes off when the charge is completed. Unbolting Key A. Unbolting key with two rods. 2. Subscription and activation of the ColumbaTD ser vice The ColumbaTD must be activated in order to be oper ational. This activation requires a subscription to the medical tele-security service offered in France by Medical Mobile. The subscription general conditions and the tele-se curity medical service subscription formulary are i nside this box. Those documents must be fully read, understood, and compl eted before being returned to the address indicated on the documents. On the days following the reception of the formular y, a representative will contact the subscriber to complete the activation of the ColumbaTD system. BEFORE THE REPRESENTATIVE CALLS, THE COLUMBATD SYSTEM MUST HAVE BEING PUT IN PLACE AND CHARGE ACCORDING TO THE INSTRUCTION IN THE FOLL OWING SECTION. During the call of a Medical Mobile representative, if the tests executed by the representative are co ncluding, the representative will confirm the activation of the ColumbaTD service. It is only at the moment of this confirmation by a Me dical Mobile representative, that the ColumbaTD is operational and the ColumbaTD service is activated. 3. Installation of the ColumbaTD system 3.1. Choice and installation of the bracelet The ColumbaTD system contains two bracelets of diff erent size, allowing better adaption to different w rist circumferences. Moreover, each bracelet has many possible adjustments, to pro cure superior comfort and maximum security to the w earer. To select the best suited bracelet, wrap each aroun d the wearer’s wrist. Choose the bracelet which rod (extremity of the bracelet that goes in the lock) is near the holes on the other ex tremity of the bracelet. Once the appropriate bracelet is chosen, it must be inserted in the slits under the ColumbaTD. It is p referable to place the ColumbaTD in the middle of the bracelet. This step completed, then the lock must installed i n the perforated extremity of the bracelet, using t he screwdriver include in the package. The lock must be screwed near the holes pr eviously identified. 3. Installation of the ColumbaTD System Then, install the bracelet with the ColumbaTD aroun d the wrist of the wearer, and identify the bracele t openings in which the lock must be screwed. The openings must be chosen in ord er to prevent the wearer from taking the bracelet o ff without unbolting the lock. Be sure the wearer is comfortable enough and tha…

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ASSESSMENT SUMMARY Order No: 6C65294 Assessor: Russell Grant Issue Date: 30 Mar. 07 Cert/Check/005.doc Page 1 of 2 July 2004 Nemko Canada Inc., 303 River Road, Ottawa, Ontario, K1V 1H2, Canada Tel: +1 613 737 9680, email: [email protected] , web: www.nemko.com Applicant Name: Medical Intelligence Product Name: Model: CLM-BRA-001 Bracelet Certification Number: (FCC ID or IC:) FCC ID: TV9-MICLM-C001 Customer Reference No: Columba Bracelet FCC Questions Applicant Response 1) Per Suppl. C, SAR tests should use normal operation power source, rather than external power suppl! y. If not in exhibits already, please explain use of external supply, effects of leads on exposure conditions, etc. "The use of external DC power adapters or other signal leads that are not normally required during normal use should be avoided because they may perturb the field and change the exposure conditions." "Unless an external DC power adapter or other signal leads are required for the normal operation of a device, such as connecting a headset to the device for body-worn use, they should not be used in the SAR tests." Response: At the time of the EMC and SAR certification testing the manufacturer did not have a charging unit that was capable of fully charging the internal battery and therefore a power supply was used for the evaluations. The power supply leads may affect the SAR distribution and power drift; however we would expect any change in SAR to be negligible and would not change the measured levels significantly. The measured SAR levels are considerably low and therefore a marginal change in the SAR levels would not result in an issue of non-compliance with the SAR limit. 2) In this PBA stage, please submit internal photos showing antenna, chassis assy, etc Response: Please refer to internal photograph exhibits: • Internal Photos • Battery • Antenna 3) It is somewhat unclear how flat-phantom setup would be representative for wrist-worn device with curved back face creating a relatively large air-gap that would not be present in normal use, also depending on device design, antenna position, etc. For some curved-back-face large-gap conditions, some testing for example in SAM twin-phantom neck region may be appropriate. Response: Please refer to the following supplementary engineering test report for SAR measurements made in the neck region of the SAM twin phantom: • Addendum Columba SAR Report • Addendum 835MHz System Validation Body • Addendum 1900MHz System Validation Body • Addendum ET3DV6-1387 Probe Calibration • Addendum EX3DV4-3600 Probe Calibration CERTIFICATION CHECK LIST Page 2 of 2 4) Usr man has CLC not FCC - if marketing and operation in US are intended, such that FCC grant is appropriate, operating and RF exposure info should be relative to FCC RF exposure requirements. Response: Please refer to page 21 of revised user manual exhibit USERGUIDE-4us The applicant has included the following USA/Canada RF exposure compliance statement: “The Medical Intelligence Technologies Inc. Model: Columba PCS/Cellular GSM/GPRS Wrist-Worn Personal Location device FCC ID: TV9-MICLM-C001 complies with SAR (Specific Absorption Rate) RF exposure requirements specified in FCC 47 CFR 2.1093 and Health Canada’s Safety Code 6 for the General Population / Uncontrolled Exposure Environment.” 5) If not in exhibits already, per 2.1046 please provide info about measured or nominal conducted output power Response: Plase refer to page 10 of Test Report Part 24E 1900 MHz output power is 30.66 dBm EIRP and page 12 of Test Report 22H 800 MHz output power is 19.5 dBm, and on page 34 radiated output power is 22.57 dBm ERP See page 4 of Columba FCC-IC SAR Report 6) If not in exhibits already, please provide info about user control or automatic mechanisms to transmit data – 1 call a week or 10 calls a day for what durations, source-based time-averaging considerations Response: Please refer to Bracelet Operational Description for a description user controls and call duration. 7) If not in exhibits already, please provide info about whether and how other operating configurations and exposure conditions (1-g SAR) may apply besides wrist-worn 10-g SAR Response: This device functions as a speaker-phone for voice communications and is not intended or required to be held in close proximity to the face. 1 gram body-worn SAR levels are reported to show compliance if the device were worn further up the arm than at the wrist. 8) User man mentions "2.402 GHz, maximum power 10 dB", but other info not found - please explain Response: See page 18 of revised user manual USERGUIDE-4us. This equipment does not transmit 2.4 GHz it can only receive 2.4 GHz from an another device FCC ID: TV9- MICLM-B001 that will be certified under 15.249 TX 2.4 GHz.

Top Side of DUT

MOD: CLM-BRA-001 06-16-01-01-xxxxxxxx Fabriqué au/made in Canada IC: 6387A-CLMBRA01 FCC ID: TV9-MICLM-C001

Main-board (with GSM-module) – Top Main-board (with GSM-module) – Top Main-board– Bottom (inside GSM-module) GSM-antenna Top-board with GPS-RX – Top Top-board with GPS-RX – Bottom

Company: Medical Intelligence Technologies Inc. Model: Columba FCC ID: TV9-MICLM-C001 DUT Type: PCS/Cellular GSM/GPRS Wrist-Worn Personal Location Device IC ID: 6387A-CLMBRA01 2006 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc.Page 1 of 36 Test Report Serial No.: 033106TV9-T735-S24G Test Report Revision No.: Revision 1.2 Dates of Evaluation: April 05-06, 2006 Test Report Issue Date: December 13, 2006 Type of Evaluation: RF Exposure SAR FCC 47 CFR §2.1093 IC RSS-102 Issue 2 Test Report Prepared By: Cheri Frangiadakis Test Report Writer Celltech Labs Inc. Test Report Approved By: Jonathan Hughes General Manager Celltech Labs Inc. RF EXPOSURE EVALUATION SPECIFIC ABSORPTION RATE S S S A A A R R R T T T E E E S S S T T T R R R E E E P P P O O O R R R T T T FOR MEDICAL INTELLIGENCE TECHNOLOGIES INC. WRIST-WORN PERSONAL LOCATION DEVICE MODEL: COLUMBA FCC ID: TV9-MICLM-C001 IC ID: 6387A-CLMBRA01 Test Report Serial No. 033106TV9-T735-S24G Test Report Revision No. Revision 1.2 - 3rd Release (Recalculated ERP for 300 kHz RBW) Test Lab and Location Celltech Compliance Testing & Engineering Lab (Celltech Labs Inc.) 1955 Moss Court Kelowna, BC Canada V1Y 9L3 Company: Medical Intelligence Technologies Inc. Model: Columba FCC ID: TV9-MICLM-C001 DUT Type: PCS/Cellular GSM/GPRS Wrist-Worn Personal Location Device IC ID: 6387A-CLMBRA01 2006 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc.Page 2 of 36 Test Report Serial No.: 033106TV9-T735-S24G Test Report Revision No.: Revision 1.2 Dates of Evaluation: April 05-06, 2006 Test Report Issue Date: December 13, 2006 Type of Evaluation: RF Exposure SAR FCC 47 CFR §2.1093 IC RSS-102 Issue 2 Celltech Labs Inc. declares under its sole responsibility that this wireless device was compliant with the Specific Absorption Rate (SAR) RF exposure requirements specified in FCC 47 CFR §2.1093 and Health Canada’s Safety Code 6. The device was tested in accordance with the measurement standards and procedures specified in FCC OET Bulletin 65, Supplement C (Edition 01-01) and Industry Canada RSS-102 Issue 2 for the General Population / Uncontrolled Exposure environment. All measurements were performed in accordance with the SAR system manufacturer recommendations. I attest to the accuracy of data. All measurements were performed by me or were made under my supervision and are correct to the best of my knowledge and belief. I assume full responsibility for the completeness of these measurements and vouch for the qualifications of all persons taking them. This test report shall not be reproduced partially, or in full, without the prior written approval of Celltech Labs Inc. The results and statements contained in this report pertain only to the device(s) evaluated. DECLARATION OF COMPLIANCE SAR RF EXPOSURE EVALUATION Test Lab and Location CELLTECH LABS INC. Testing and Engineering Services 1955 Moss Court Kelowna, B.C. Canada V1Y 9L3 Phone: 250-448-7047 Fax: 250-448-7046 e-mail: [email protected] web site: www.celltechlabs.com Company Information MEDICAL INTELLIGENCE TECHNOLOGIES INC. 1170 Grande-Allée Ouest Québec (Quebec) G1S 1E5 Canada FCC IDENTIFIER: TV9-MICLM-C001 IC IDENTIFIER: 6387A-CLMBRA01 Model(s): Columba SAR Test Requirement(s): FCC 47 CFR §2.1093; Health Canada Safety Code 6 SAR Test Procedure(s): FCC OET Bulletin 65, Supplement C (Edition 01-01) Industry Canada RSS-102 Issue 2 FCC Device Classification: PCS Licensed Transmitter worn on body (PCT) IC Device Classification: 2 GHz Personal Communication Services (RSS-133 Issue 3) Cellular Telephones Employing New Technologies (RSS-132 Issue 2) Device Description: Dual-Band PCS/Cellular GSM/GPRS Wrist-Worn Personal Location Device Transmit Frequency Range(s): 1850.2 - 1909.8 MHz (PCS GSM) 824.2 - 848.8 MHz (Cellular GSM) Max. RF Output Power Tested: 30.66 dBm (1.16 W) EIRP (PCS GSM) 22.57 dBm (180.79 mW) ERP (Cellular GSM) Max. Duty Cycle Tested: 24 % (Source-Based Time-Averaged) Max. SBTA RF Output Power: 24.45 dBm (278.4 mW) EIRP (PCS GSM) 16.37 dBm (43.39 mW) ERP (Cellular GSM) Data Transmission Type: GPRS Class B, Multislot Class 10 Antenna Type(s) Tested: Internal PCB Antenna Power Source(s) Tested: External Power Supply (4.1 VDC) Internal Battery Type(s): Lithium-Polymer (3.7 V, 570 mAh) Max. SAR Level(s) Evaluated: Wrist: 0.033 W/kg (PCS); 0.00208 W/kg (Cellular) - 10g average Body: 0.054 W/kg (PCS); 0.00321 W/kg (Cellular) - 1g average Test Report Approved By: Sean Johnston SAR Lab Manager Celltech Labs Inc. Company: Medical Intelligence Technologies Inc. Model: Columba FCC ID: TV9-MICLM-C001 DUT Type: PCS/Cellular GSM/GPRS Wrist-Worn Personal Location Device IC ID: 6387A-CLMBRA01 2006 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc.Page 3 of 36 Test Report Serial No.: 033106TV9-T735-S24G Test Report Revision No.: Revision 1.2 Dates of Evaluation: April 05-06, 2006 Test Report Issue Date: December 13, 2006 Type of Evaluation: RF Exposure SAR FCC 47 CFR §2.1093 IC RSS-102 Issue 2 TABLE OF CONTENTS 1.0 INTRODUCTION __________________________________________________________________ 4 2.0 DESCRIPTION of DEVICE UNDER TEST (DUT)_________________________________________ 4 3.0 SAR MEASUREMENT SYSTEM ______________________________________________________ 5 4.0 MEASUREMENT SUMMARY ________________________________________________________ 6 5.0 DETAILS OF SAR EVALUATION _____________________________________________________ 8 6.0 EVALUATION PROCEDURES _______________________________________________________ 8 7.0 SYSTEM PERFORMANCE CHECK ___________________________________________________ 9 8.0 SIMULATED EQUIVALENT TISSUES _________________________________________________ 10 9.0 SAR SAFETY LIMITS _____________________________________________________________ 10 10…

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Company: Medical Intelligence Technologies Inc. Model: Columba FCC ID: TV9-MICLM-C001 DUT Type: PCS/Cellular GSM/GPRS Wrist-Worn Personal Location Device IC ID: 6387A-CLMBRA01 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 1 of 12 SAR Test Report Addendum (Response to TCB) Report Addendum No.: S735A-032707-R1.0 Date(s) of Evaluation: March 13 & 26, 2007 Test Report Serial No. 033106TV9-T735-S24G Type of Evaluation: RF Exposure SAR FCC OET 65, Supp. C IC RSS-102 Issue 2 BODY/WRIST SAR EVALUATION RESULTS (DUAL-BAND GPRS) EIRP/ERP Start Power (dBm) Body SAR 1g (W/kg) Wrist SAR 10g (W/kg) Freq. (MHz) Chan. Test Mode Power Source Phantom Section DUT Position to Planar Phantom DUT Spacing to Planar Phantom Measured SBTA Measured Scaled 1 Measured Scaled 1 1880.0 661 PCS GPRS 2 Slots 4.1 VDC SAM-Twin Left Neck Bottom Side Touc h 30.66 EIRP 24.45 EIRP 0.111 0.118 0.0661 0.0705 836.6 190 Cellular GPRS 2 slots 4.1 VDC SAM-Twin Left Neck Bottom Side Touc h 22.57 ERP 16.37 ERP 0.00126 - 0.000648 - ANSI / IEEE C95.1-2005 SAFETY LIMIT: WRIST: 4.0 W/kg (averaged over 10 grams) BODY: 1.6 W/kg (averaged over 1 gram) Spatial Peak Uncontrolled Exposure / General Population Test Date(s) PCS GPRS: March 13, 2007 Cellular GPRS: March 26, 2007 Measured Fluid Type 1880 MHz 835 MHz Unit 1880 MHz Body 835 MHz Body Relative Humidity 32 31 % IEEE Target Meas. Dev. IEEE Target Meas. Dev. Atmospheric Pressure 102.1 101.4 kPa Dielectric Constant ε r 53.3 ± 5% 50.7 -4.8% 55.2 ± 5% 56.6 +2.6% Ambient Temperature 22.9 22.6 °C 1880 MHz Body 835 MHz Body Fluid Temperature 20.9 21.6 °C IEEE Target Meas. Dev. IEEE Target Meas. Dev. Fluid Depth ≥ 15 ≥ 15 cm Conductivity σ (mho/m) 1.52 ± 5% 1.54 +1.4% 0.97 ± 5% 0.98 +1.1% ρ (Kg/m 3 ) 1000 1. The SAR level measured at the mid channel for PCS band was scaled up by 0.28 dB to report an estimated increase in the SAR level based on the difference in output power (EIRP) that was measured for the low channel (see page 7 of Celltech SAR Test Report S/N: 033106TV9-T735-S24G Rev. 1.2 for EIRP measurement results). 2. If the measured SAR levels evaluated at the mid channel were ≥ 3 dB below the SAR limit, SAR evaluation for the low and high channels was optional (per FCC OET Bulletin 65, Supplement C, Edition 01-01 - see reference [3]). 3. The fluid temperature was measured prior to and after the SAR evaluation to ensure the temperature remained within +/-2°C of the fluid temperature reported during the dielectric parameter measurements. 4. The dielectric parameters of the simulated tissue mixtures were measured prior to the SAR evaluations using an ALS-PR-DIEL Dielectric Probe Kit and an HP 8753ET Network Analyzer (see Appendix C). Note(s) 5. The SAR measurements were performed within 24 hours of the system performance check. SYSTEM PERFORMANCE CHECK EVALUATIONS Tissue SAR 1g (W/kg) Dielectric Constant ε r Conductivity σ (mho/m) Test Date MHz SPEAG Target Meas. Dev. IEEE Target Meas. Dev. IEEE Target Meas. Dev. ρ (Kg/m 3 ) Amb. Temp. (°C) Fluid Temp. (°C) Fluid Depth (cm) Humid. (%) Barom. Press. (kPa) 3/13/07 1900 Body 9.95 ±10% 10.7 +7.6% 53.3 ±5% 50.6 -5.0% 1.52 ±5% 1.56 +2.7% 1000 22.9 20.9 ≥ 15 102.1 32 3/26/07 835 Body 2.43 ±10% 2.31 -4.9% 55.2 ±5% 56.6 +2.6% 0.97 ±5% 0.98 +1.1% 1000 22.6 21.6 ≥ 15 101.4 31 Company: Medical Intelligence Technologies Inc. Model: Columba FCC ID: TV9-MICLM-C001 DUT Type: PCS/Cellular GSM/GPRS Wrist-Worn Personal Location Device IC ID: 6387A-CLMBRA01 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 2 of 12 SAR Test Report Addendum (Response to TCB) Report Addendum No.: S735A-032707-R1.0 Date(s) of Evaluation: March 13 & 26, 2007 Test Report Serial No. 033106TV9-T735-S24G Type of Evaluation: RF Exposure SAR FCC OET 65, Supp. C IC RSS-102 Issue 2 Date Tested: 03/13/2007 Body/Wrist-Worn SAR - Bottom Side of DUT - PCS GPRS - 1880.0 MHz - Channel 661 DUT: Medical Intelligence Columba; Type: Dual-Band GSM/GPRS Wrist-Worn Personal Location Device; Serial: None Ambient Temp: 22.9°C; Fluid Temp: 20.9°C; Barometric Pressure: 102.1 kPa; Humidity: 32% Power Source: 4.1 VDC External RF Output Power: 30.66 dBm (EIRP) Frequency: 1880.0 MHz; Duty Cycle: 1:4.16 Communication System: PCS GPRS (2 Time Slots) Medium: M1880 Medium parameters used: f = 1880 MHz; σ = 1.54 mho/m; ε r = 50.7; ρ = 1000 kg/m 3 - Probe: EX3DV4 - SN3600; ConvF(6.54, 6.54, 6.54); Calibrated: 24/01/2007 - Sensor-Surface: 4mm (Mechanical Surface Detection) - Electronics: DAE4 Sn353; Calibrated: 21/06/2006 - Phantom: SAM 4.0; Type: Fiberglas; Serial: 1033 - Measurement SW: DASY4, V4.7 Build 44; Postprocessing SW: SEMCAD, V1.8 Build 171 SAR - PCS GPRS - Bottom Side of DUT Touching Left Neck Section of SAM Phantom - Channel 661 - 1880 MHz Area Scan (8x14x1): Measurement grid: dx=10mm, dy=10mm SAR - PCS GPRS - Bottom Side of DUT Touching Left Neck Section of SAM Phantom - Channel 661 - 1880 MHz Zoom Scan (7x7x7)/Cube 0: Measurement grid: dx=5mm, dy=5mm, dz=5mm Reference Value = 0.763 V/m Peak SAR (extrapolated) = 0.186 W/kg SAR(1 g) = 0.111 mW/g; SAR(10 g) = 0.0661 mW/g Maximum value of SAR (measured) = 0.122 mW/g Company: Medical Intelligence Technologies Inc. Model: Columba FCC ID: TV9-MICLM-C001 DUT Type: PCS/Cellular GSM/GPRS Wrist-Worn Personal Location Device IC ID: 6387A-CLMBRA01 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 3 of 12 SAR Test Report Addendum (Response to TCB) Report Addendum No.: S735A-032707-R1.0 Date(s) of Evaluation: March 13 & 26, 2007 Test Report Serial No. 033106TV9-T735-S24G Type of Evaluation: RF Exposure SAR FCC OET 65, Supp. C IC RSS-102 Issue 2 Z-Axis Scan Company: Medical Intelligence Technologies Inc. Model: Columba FCC ID: TV9-MICLM-C001 DUT Type: PCS/Cellular GSM/GPRS Wrist-W…

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Celltech Labs Inc. 1955 Moss Court, Kelowna, B.C. Canada V1Y 9L3 Tel. 250-448-7047 • Fax. 250-448-7046 • e-mail: [email protected] www.celltechlabs.com 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 1 of 10 Date of Evaluation: March 26, 2007 Document Serial No.: SV835M-032607-R1.0 Evaluation Type: System Validation Validation Dipole: 835 MHz Fluid Type: Body 835 MHz SYSTEM VALIDATION Type: Asset Number: Serial Number: Place of Validation: Date of Validation: Celltech Labs Inc. hereby certifies that the 835 MHz System Validation was performed on the date indicated above. Performed by: Approved by: 835 MHz Validation Dipole 411 Celltech Labs Inc. March 26, 2007 00022 Sean Johnston Spencer Watson 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 2 of 10 Date of Evaluation: March 26, 2007 Document Serial No.: SV835M-032607-R1.0 Evaluation Type: System Validation Validation Dipole: 835 MHz Fluid Type: Body 1. Validation Dipole Construction & Electrical Characteristics The validation dipole was constructed in accordance with the IEEE Standard “Annex G (informative) Reference dipoles for use in system validation”. The electrical properties were measured using an HP 8753ET Network Analyzer. The network analyzer was calibrated to the validation dipole N-type connector feed point using an HP85032E Type N calibration kit. The dipole was placed parallel to a planar phantom at a separation distance of 15.0mm from the simulating fluid using a loss-less dielectric spacer. The measured input impedance is: Feed point impedance at 835 MHz Re{Z} = 50.695Ω Im{Z} = -2.7656Ω Return Loss at 835 MHz -31.282dB 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 3 of 10 Date of Evaluation: March 26, 2007 Document Serial No.: SV835M-032607-R1.0 Evaluation Type: System Validation Validation Dipole: 835 MHz Fluid Type: Body 2. Validation Dipole VSWR Data 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 4 of 10 Date of Evaluation: March 26, 2007 Document Serial No.: SV835M-032607-R1.0 Evaluation Type: System Validation Validation Dipole: 835 MHz Fluid Type: Body 3. Validation Dipole Dimensions Frequency (MHz) L (mm) h (mm) d (mm) 300 420.0 250.0 6.2 450 288.0 167.0 6.2 835 161.0 89.8 3.6 900 149.0 83.3 3.6 1450 89.1 51.7 3.6 1800 72.0 41.7 3.6 1900 68.0 39.5 3.6 2000 64.5 37.5 3.6 2450 51.8 30.6 3.6 3000 41.5 25.0 3.6 4. Validation Phantom The validation phantom is a Fiberglass shell planar phantom manufactured by Barski Industries Ltd. The phantom is in conformance with the requirements defined by IEEE SCC34-SC2 for the dosimetric evaluations of body-worn and lap-held operating configurations. Reference markings on the phantom allow the complete setup of all predefined phantom positions and measurement grids. Shell Thickness: 2.0 ± 0.1 mm Filling Volume: Approx. 55 liters Dimensions: 44 cm (W) x 94 cm (L) 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 5 of 10 Date of Evaluation: March 26, 2007 Document Serial No.: SV835M-032607-R1.0 Evaluation Type: System Validation Validation Dipole: 835 MHz Fluid Type: Body 5. 835 MHz System Validation Setup 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 6 of 10 Date of Evaluation: March 26, 2007 Document Serial No.: SV835M-032607-R1.0 Evaluation Type: System Validation Validation Dipole: 835 MHz Fluid Type: Body 6. 835 MHz Validation Dipole Setup 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 7 of 10 Date of Evaluation: March 26, 2007 Document Serial No.: SV835M-032607-R1.0 Evaluation Type: System Validation Validation Dipole: 835 MHz Fluid Type: Body 7. SAR Measurement Measurements were made using a dosimetric E-field probe ET3DV6 (S/N: 1387, Conversion Factor 6.18). The SAR measurement was performed with the E-field probe in mechanical detection mode only. The setup and determination of the forward power into the dipole was performed using the following procedures. PM1 Att1 x Dipole 3D Probe positioner Flat Phantom Field probe Signal Generator AmpLow Pass 3dB Att3 Dir.Coupler Att2 PM2 Cable PM3 d First the power meter PM1 (including attenuator Att1) is connected to the cable to measure the forward power at the location of the dipole connector (X). The signal generator is adjusted for the desired forward power at the dipole connector (taking into account the attenuation of Att1) as read by power meter PM2. After connecting the cable to the dipole, the signal generator is readjusted for the same reading at power meter PM2. If the signal generator does not allow adjustment in 0.01dB steps, the remaining difference at PM2 must be taken into consideration. PM3 records the reflected power from the dipole to ensure that the value is not changed from the previous value. The reflected power should be 20dB below the forward power. 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 8 of 10 Date of Evaluation: March 26, 2007 Document Serial No.: SV835M-032607-R1.0 Evaluation Type: System Validation Validation Dipole: 835 MHz Fluid Type: Body 8. Measurement Conditions The planar phantom was filled with 835 MHz body tissue simulant. Relative Permittivity: 56.6 (+2.6% from target) Conductivity: 0.98 mho/m (+1.1% from target) Fluid Temperature: 21.6 °C Fluid Depth: ≥ 15.0 cm Environmental Conditions: Ambient Temperature: 22.6…

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Celltech Labs Inc. 1955 Moss Court, Kelowna, B.C. Canada V1Y 9L3 Tel. 250-448-7047 • Fax. 250-448-7046 • e-mail: [email protected] www.celltechlabs.com 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Celltech Labs Inc. Page 1 of 10 Date of Evaluation: February 02, 2007 Document Issue No.: SV1900M-020207-R1.1 Evaluation Type: System Validation Validation Dipole: 1900 MHz Fluid Type: Body 1900 MHz SYSTEM VALIDATION Type: Asset Number: Serial Number: Place of Validation: Date of Validation: Celltech Labs Inc. certifies that the 1900 MHz System Validation was performed on the date indicated above. Performed by: Approved by: 1900 MHz Validation Dipole 151 February 02, 2007 00032 Celltech Labs Inc. Sean Johnston Spencer Watson 2007 Celltech Labs Inc. This document is not to be reproduced in whole or in part without the prior written permission of Ce…

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