
Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.
Revision 0.3 Document No. 11573 Page 1 Aera CT Mobile Cardiac Monitor Operator Manual Revision 0.3 Document No. 11573 Page 2 Contents Device Overview ........................................................................................................................................................3 Description .......................................................................................................................................................................... 3 Indications for Use .............................................................................................................................................................. 4 Contraindications ................................................................................................................................................................ 4 Recorder Components ........................................................................................................................................................ 5 Equipment Symbols ............................................................................................................................................................ 7 Precautions ......................................................................................................................................................................... 8 Operation ..................................................................................................................................................................9 Initial Device Setup ............................................................................................................................................................. 9 User Interface ................................................................................................................................................................... 10 Starting a Study ................................................................................................................................................................. 11 Monitoring a Study ........................................................................................................................................................... 16 Ending a Study ................................................................................................................................................................... 18 Electrode Application ........................................................................................................................................................ 21 Patient Use Precautions .................................................................................................................................................... 23 Maintenance ........................................................................................................................................................... 24 Charging ............................................................................................................................................................................ 24 Storage .............................................................................................................................................................................. 24 Cleaning ............................................................................................................................................................................. 26 Testing ............................................................................................................................................................................... 26 Troubleshooting ...................................................................................................................................................... 27 Error Messages.................................................................................................................................................................. 27 Server Errors ..................................................................................................................................................................... 28 Wireless Compliance ................................................................................................................................................ 29 Specifications ........................................................................................................................................................... 31 TZ Medical Warranty ................................................................................................................................................ 33 Limited Warranty ..................................................................................................................................................... 33 Obtaining Warranty Service ..................................................................................................................................... 33 Accessories .............................................................................................................................................................. 34 Revision 0.3 Document No. 11573 Page 3 Device Overview Description Caution: US Federal law restricts this device to sale by or on the order of a physician. The Aera CT is a battery operated ambulatory electrocardiograph recorder for use in mobile cardiovascular telemetry. It is capable of storing 3 channels of patient ECG data acquired from three or five surface electrodes adhered to the body for over 28 days of continuous recording. The Aera CT employs a rechargeable Lithium- Ion battery to achieve such an extended recording duration. The Aera CT provides the ability to automatically detect and record pacemaker pulses as well as several common arrhythmias in accordance with the applicable standards of th…
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7272 SW Durham Road • Suite 800 • Portland, OR 97224 • Facsimile 503.639.0239 • www.TZmedical.com Date: February 14, 2012 Federal Communications Commission Authorization and Evaluation Division 7435 Oakland Mills Road Columbia, MD 21046 Attn: OET Dept. Ref: FCC ID: ZIMTZMR Applicant: TZ Medical, Inc. Dear Examiner, We the undersigned, hereby authorize Heiko Strehlow, Director of Regulatory and Antenna Services (Cetecom, Inc., 411 Dixon Landing Road, Milpitas, CA 95035, Tel.408 586 6214) to act on our behalf in all manners relating to application for equipment authorization, including signing of all documents relating to these matters. Any and all acts carried out by CETECOM Inc., on our behalf shall have the same effect as acts of our own. The authorization from TZ Medical, Inc., is valid for 90 days from the date of this letter. Sincerely, John Lubisich President TZ Medical, Inc. 17750 SW Upper Boones Ferry Rd. #150 Portland, OR 97224
17750 SW Upper Boones Ferry Rd • Suite 150 • Portland, OR 97224 • Facsimile 503.639.0239 • www.TZmedical.com Federal Communication Commission Equipment Authorization Division, Application Processing Branch February 14, 2012 7435 Oakland Mills Road Columbia, MD 21048 Subject:Request for Confidentiality FCC ID: ZIMTZMR To Whom It May Concern: Pursuant to the provisions of Sections 0.457 and 0.459 of the Commission’s rules (47 CFR §§ 0.457, 0.459), TZ Medical, Inc. hereby requests confidential treatment of the following attachments and request that the Commission withhold these documents from public disclosure indefinitely. Schematics, Block Diagrams, Bill of Materials, Operational Description, Tune Up Procedure, Antenna Specification The documents mentioned above contain proprietary information and public disclosure of these documents might be harmful to our company and could give our competitors an unfair advantage. In addition to above mentioned documents, pursuant to Public Notice DA 04‐1705 of the Commission’s policy, in order to comply with the marketing regulations in 47 CFR §2.803 and the importation rules in 47 CFR §2.1204, while ensuring that business sensitive information remains confidential until the actual marketing of newly authorized devices, TZ Medical, Inc. hereby requests short‐term confidentiality on the following attachments for 180 days, from the day the grant is issued. External Photos, Internal Photos, Test Setup Photos, and User Manual It is our understanding that all measurement test reports, FCC ID label format and correspondence during the certification review process will be available for public review once the grant of equipment authorization is issued. If you have any questions, please feel free to contact me at the address shown below. Sincerely, Name: John Lubisich, President Company: TZ Medical, Inc. Address: 17750 SW Upper Boones Ferry Rd. #150 Portland, OR 97224 Phone: (800) 944‐0187 x203 Email: [email protected]
17750 SW Upper Boones Ferry Rd • Suite 150 • Portland, OR 97224 • Facsimile 503.639.0239 • www.TZmedical.com Federal Communication Commission Equipment Authorization Division, Application Processing Branch February 14, 2012 7435 Oakland Mills Road Columbia, MD 21048 Subject:Request for Confidentiality FCC ID: ZIMTZMR To Whom It May Concern: Pursuant to the provisions of Sections 0.457 and 0.459 of the Commission’s rules (47 CFR §§ 0.457, 0.459), TZ Medical, Inc. hereby requests confidential treatment of the following attachments and request that the Commission withhold these documents from public disclosure indefinitely. Schematics, Block Diagrams, Bill of Materials, Operational Description, Tune Up Procedure, Antenna Specification The documents mentioned above contain proprietary information and public disclosure of these documents might be harmful to our company and could give our competitors an unfair advantage. In addition to above mentioned documents, pursuant to Public Notice DA 04‐1705 of the Commission’s policy, in order to comply with the marketing regulations in 47 CFR §2.803 and the importation rules in 47 CFR §2.1204, while ensuring that business sensitive information remains confidential until the actual marketing of newly authorized devices, TZ Medical, Inc. hereby requests short‐term confidentiality on the following attachments for 180 days, from the day the grant is issued. External Photos, Internal Photos, Test Setup Photos, and User Manual It is our understanding that all measurement test reports, FCC ID label format and correspondence during the certification review process will be available for public review once the grant of equipment authorization is issued. If you have any questions, please feel free to contact me at the address shown below. Sincerely, Name: John Lubisich, President Company: TZ Medical, Inc. Address: 17750 SW Upper Boones Ferry Rd. #150 Portland, OR 97224 Phone: (800) 944‐0187 x203 Email: [email protected]
External Photos Top View Bottom View Side View-1 Side View-2 Side View-3 Side View-4
A��� CT Portland, OR 97224 FCC ID: ZIMTZMR IC: 9647A-TZMR Model: TZMR TZ Medical Spark ed by your ideas 0459 0682 RX Only IMEI: 1234567891234567 FCC ID: 1234564 1234564 Barcode SN: 8000001 Front Label - .01“ Scratch Resistant Polycarbonate, - Speaker and mic holes, display window, LED‘s show through - ~.002“ Adhesive Back Label - .01“ Scratch Resistant Polycarbonate - Serial label window - ~.002“ Adhesive Display protector - .03“ Polycarbonate - ~.002“ Adhesive border, no graphics Cap touch spacer - .03“ Polycarbonate - No adhesive Note: Reduce outer die-line dimensions to t case RX Only FCC ID: ZIMTZMR IC: 9647A-TZMR Model: TZMR 0459 0682 Distributed by Philips Manufactured by TZ Medical Portland, OR 97224 IMEI: 1234567891234567 FCC ID: 1234564 1234564 Barcode SN: 8000001 Front Label - .01“ Scratch Resistant Polycarbonate, - Speaker and mic holes, display window, LED‘s show through - ~.002“ Adhesive Back Label - .01“ Scratch Resistant Polycarbonate - Serial label window - ~.002“ Adhesive Display protector - .03“ Polycarbonate - ~.002“ Adhesive border, no graphics Cap touch spacer - .03“ Polycarbonate - No adhesive Note: Reduce outer die-line dimensions to t case
A��� CT Portland, OR 97224 FCC ID: ZIMTZMR IC: 9647A-TZMR Model: TZMR TZ Medical Spark ed by your ideas 0459 0682 RX Only IMEI: 1234567891234567 FCC ID: 1234564 1234564 Barcode SN: 8000001 Front Label - .01“ Scratch Resistant Polycarbonate, - Speaker and mic holes, display window, LED‘s show through - ~.002“ Adhesive Back Label - .01“ Scratch Resistant Polycarbonate - Serial label window - ~.002“ Adhesive Display protector - .03“ Polycarbonate - ~.002“ Adhesive border, no graphics Cap touch spacer - .03“ Polycarbonate - No adhesive Note: Reduce outer die-line dimensions to t case RX Only FCC ID: ZIMTZMR IC: 9647A-TZMR Model: TZMR 0459 0682 Distributed by Philips Manufactured by TZ Medical Portland, OR 97224 IMEI: 1234567891234567 FCC ID: 1234564 1234564 Barcode SN: 8000001 Front Label - .01“ Scratch Resistant Polycarbonate, - Speaker and mic holes, display window, LED‘s show through - ~.002“ Adhesive Back Label - .01“ Scratch Resistant Polycarbonate - Serial label window - ~.002“ Adhesive Display protector - .03“ Polycarbonate - ~.002“ Adhesive border, no graphics Cap touch spacer - .03“ Polycarbonate - No adhesive Note: Reduce outer die-line dimensions to t case
SAR Test Report No.: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix A Plots Page 1 of 11 Plot 1: Date/Time: 2/13/2012 4:09:32 PM Test Laboratory: Cetecom Inc. SAR 1 Lab DUT: TZ Medical; Type: Not Specified; Serial: 1024009 Communication System: GPRS-FDD (2 Timeslots); Frequency: 836.6 MHz Medium: MSL900_Batch 100818-1 Medium parameters used: f = 836.6 MHz; σ = 1 mho/m; ε r = 54.02; ρ = 1000 kg/m 3 Phantom section: Flat Section Measurement Standard: DASY5 (IEEE/IEC/ANSI C63.19-2007) Procedure Notes: Test Technician: ;kathy tran Air Temperature: ;22.5C Medium Temperature: ;21.2C Comments: ; DASY Configuration: • Probe: ES3DV3 - SN3244; ConvF(6.21, 6.21, 6.21); • Sensor-Surface: 3mm (Mechanical Surface Detection), z = 2.0, 32.0 • Electronics: DAE4 Sn1233; Calibrated: 10/13/2010 • Phantom: ELI 4.0; Type: QDOVA001BB; Serial: 1092 • DASY52 52.8.0(692); Flat-Section/Front 0mm with White holster_GPRS 2 UP TS-836.6MHz/Area Scan (11x8x1): Measurement grid: dx=15mm, dy=15mm Maximum value of SAR (measured) = 0.735 mW/g Flat-Section/Front 0mm with White holster_GPRS 2 UP TS-836.6MHz/Zoom Scan (7x7x7)/Cube 0: Measurement grid: dx=5mm, dy=5mm, dz=5mm Reference Value = 20.630 V/m; Power Drift = -0.16 dB Peak SAR (extrapolated) = 1.0260 SAR(1 g) = 0.650 mW/g; SAR(10 g) = 0.415 mW/g Maximum value of SAR (measured) = 0.776 mW/g 0 dB = 0.780mW/g = -2.16 dB mW/g SAR Test Report No.: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix A Plots Page 2 of 11 Plot 2 Date/Time: 2/13/2012 4:42:45 PM Test Laboratory: Cetecom Inc. SAR 1 Lab DUT: TZ Medical; Type: Not Specified; Serial: 1024009 Communication System: GPRS-FDD (2 Timeslots); Frequency: 836.6 MHz Medium: MSL900_Batch 100818-1 Medium parameters used: f = 836.6 MHz; σ = 1 mho/m; ε r = 54.02; ρ = 1000 kg/m 3 Phantom section: Flat Section Measurement Standard: DASY5 (IEEE/IEC/ANSI C63.19-2007) Procedure Notes: Test Technician: ;kathy tran Air Temperature: 22.6C Medium Temperature: 21.2C Comments: ; DASY Configuration: • Probe: ES3DV3 - SN3244; ConvF(6.21, 6.21, 6.21); • Sensor-Surface: 3mm (Mechanical Surface Detection), z = 2.0, 32.0 • Electronics: DAE4 Sn1233; Calibrated: 10/13/2010 • Phantom: ELI 4.0; Type: QDOVA001BB; Serial: 1092 • DASY52 52.8.0(692); Flat-Section/Back 0mm with White holster_GPRS 2 UP TS_836.6MHz/Area Scan (10x9x1): Measurement grid: dx=15mm, dy=15mm Maximum value of SAR (measured) = 0.899 mW/g Flat-Section/Back 0mm with White holster_GPRS 2 UP TS_836.6MHz/Zoom Scan (8x8x7)/Cube 0: Measurement grid: dx=5mm, dy=5mm, dz=5mm Reference Value = 20.215 V/m; Power Drift = -0.17 dB Peak SAR (extrapolated) = 1.2020 SAR(1 g) = 0.799 mW/g; SAR(10 g) = 0.533 mW/g Maximum value of SAR (measured) = 0.932 mW/g 0 dB = 0.930mW/g = -0.63 dB mW/g SAR Test Report No.: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix A Plots Page 3 of 11 Plot 3 Date/Time: 2/13/2012 5:16:11 PM Test Laboratory: Cetecom Inc. SAR 1 Lab DUT: TZ Medical; Type: Not Specified; Serial: 1024009 Communication System: GPRS-FDD (2 Timeslots); Frequency: 836.6 MHz Medium: MSL900_Batch 100818-1 Medium parameters used: f = 836.6 MHz; σ = 1 mho/m; ε r = 54.02; ρ = 1000 kg/m 3 Phantom section: Flat Section Measurement Standard: DASY5 (IEEE/IEC/ANSI C63.19-2007) Procedure Notes: Test Technician: Kathy Tran; Air Temperature: 22.8C; Medium Temperature: 21.2C; Comments: ; DASY Configuration: • Probe: ES3DV3 - SN3244; ConvF(6.21, 6.21, 6.21); • Sensor-Surface: 3mm (Mechanical Surface Detection), z = 2.0, 32.0 • Electronics: DAE4 Sn1233; Calibrated: 10/13/2010 • Phantom: ELI 4.0; Type: QDOVA001BB; Serial: 1092 • DASY52 52.8.0(692); Flat-Section/Back 0mm with Black holster_GPRS 2 UP TS_836.6MHz/Area Scan (10x8x1): Measurement grid: dx=15mm, dy=15mm Maximum value of SAR (measured) = 0.410 mW/g Flat-Section/Back 0mm with Black holster_GPRS 2 UP TS_836.6MHz/Zoom Scan (7x7x7)/Cube 0: Measurement grid: dx=5mm, dy=5mm, dz=5mm Reference Value = 15.999 V/m; Power Drift = -0.15 dB Peak SAR (extrapolated) = 0.5220 SAR(1 g) = 0.365 mW/g; SAR(10 g) = 0.254 mW/g Maximum value of SAR (measured) = 0.419 mW/g 0 dB = 0.420mW/g = -7.54 dB mW/g SAR Test Report No.: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix A Plots Page 4 of 11 Plot 4 Date/Time: 2/13/2012 5:54:53 PM Test Laboratory: Cetecom Inc. SAR 1 Lab DUT: TZ Medical; Type: Not Specified; Serial: 1024009 Communication System: GSM-FDD (TDMA, GMSK); Frequency: 836.6 MHz Medium: MSL900_Batch 100818-1 Medium parameters used: f = 836.6 MHz; σ = 1 mho/m; ε r = 54.02; ρ = 1000 kg/m 3 Phantom section: Flat Section Measurement Standard: DASY5 (IEEE/IEC/ANSI C63.19-2007) Procedure Notes: Test Technician: ;kathy tran Air Temperature: ; 22.5C Medium Temperature: 21.2C Comments: ; DASY Configuration: • Probe: ES3DV3 - SN3244; ConvF(6.21, 6.21, 6.21); • Sensor-Surface: 3mm (Mechanical Surface Detection), z = 2.0, 32.0 • Electronics: DAE4 Sn1233; Calibrated: 10/13/2010 • Phantom: ELI 4.0; Type: QDOVA001BB; Serial: 1092 • DASY52 52.8.0(692); Flat-Section/Back 0mm with White holster_GPRS 1 UP TS_836.6MHz/Area Scan (10x9x1): Measurement grid: dx=15mm, dy=15mm Maximum value of SAR (measured) = 0.636 mW/g Flat-Section/Back 0mm with White holster_GPRS 1 UP TS_836.6MHz/Zoom Scan (8x8x7)/Cube 0: Measurement grid: dx=5mm, dy=5mm, dz=5mm Reference Value = 16.181 V/m; Power Drift = 0.02 dB Peak SAR (extrapolated) = 0.8510 SAR(1 g) = 0.572 mW/g; SAR(10 g) = 0.385 mW/g Maximum value of SAR (measured) = 0.659 mW/g 0 dB = 0.660mW/g = -3.61 dB mW/g SAR Test Report No.: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix A Plots Page 5 of 11 Plot 5 Date/Time: 2/16/2012 1:52:10 PM Test Laboratory: Cetecom Inc., SAR 3 Lab DUT: Aera CT; Type: TZ Medical; Serial: 1024009 Communication System: GPRS 2 Timeslots; Frequency: 1880 MHz Medium: MSL1900_Batch 100824-3 Medium paramete…
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SAR Test Report No: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix C Page 1 of 6 Tissue Parameters Recipe for liquids below 1 GHz: Water 35-58% Sugar 40-60% Salt 0-6% Hydroxyethyl-cellulose <0.3% Preventol-D7 0.1-0.7% Recipe for liquids above 1-3 GHz: Water 52-75% DGBE 25-48% Salt <1.0% SAR measurements were made within 24 hours of the measurement of liquid parameters. 850MHz Body Liquid: Date Freq. Rel. Condy (MHz) Perm. (S/m) 2012-02-13 824.2 54.2 0.986 835 54.02 0.998 836.6 54.02 1 848.8 53.84 1.012 1900MHz Body Liquid: Date Freq. Rel. Condy (MHz) Perm. (S/m) 2012-02-16 1850.2 52.36 1.461 1880 51.85 1.485 1900 51.61 1.484 1909.8 51.56 1.475 SAR Test Report No: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix C Page 2 of 6 Antenna Locations SAR Test Report No: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix C Page 3 of 6 Test Equipment SAR1 Lab Equipment Model Serial Instrument description Supplier / Manufacturer Model Serial No. Calibration (date) Calibration Due (date) Robot Staubli TX90 F10/5D3NA 1/A/01 N/A N/A SAM Twin Phantom SPEAG SM 000 T01 DA 1592 N/A N/A Eliptical Phantom SPEAG QD OVA 001 BB 1092 N/A N/A Software SPEAG Dasy52.6.2.482 N/A N/A N/A Device Holder SPEAG SD 000H01 N/A N/A N/A Data Acquisition Electronics SPEAG DAE4 1233 2010/10/13 2013/10/13 SAR Probe SPEAG ES3DV3 3244 2011/10/25 2012/10/25 SAR 3 Lab Instrument description Supplier / Manufacturer Model Serial No. Calibration (date) Calibration Due (date) Robot Staubli TX90 F11/5G2MA 1/C/01 N/A N/A SAM Twin Phantom SPEAG SM 000 T01 DA 1637 N/A N/A SAM Twin Phantom SPEAG SM 000 T01 DA 1638 N/A N/A Eliptical Phantom SPEAG QD OVA 001 BB 1124 N/A N/A Software SPEAG Dasy52.6.2.482 N/A N/A N/A Device Holder SPEAG SD 000H01 N/A N/A N/A Data Acquisition Electronics SPEAG DAE4 1266 2011/05/30 2014/05/30 SAR Probe SPEAG ES3DV3 3260 2011/05/15 2011/05/15 SAR Test Report No: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix C Page 4 of 6 Shared Equipment Instrument description Supplier / Manufacturer Model Serial No. Calibrati on (date) Calibration Due (date) 850 MHz Body Tissue Simulant SPEAG MSL 900 100818-1 2012/02/13 N/A 1900 MHz Body Tissue Simulant SPEAG MSL 1900 100824-3 2012/02/16 N/A 835 MHz Dipole SPEAG D835V2 4D113 2011-01- 10 2013-01-10 1900 MHz Dipole SPEAG D1900V2 5D135 2011-01- 05 2013-01-05 Network Analyzer Agilent E753ES US39172511 2011/06/22 2012/06/22 Calibration Kit HP 85052D 2830A00748 2011/03/22 2012/03/22 Directional coupler Werlatone C6529 11249 N/A N/A RF Amplifier Vectawave VTL5400 N/A N/A N/A Dielectric Measurement Kit IndexSAR Di-Line N/A N/A N/A Synthesized CW Generator Agilent 8371213 US37101255 N/A N/A Power Meter Agilent E4419B MY45101996 2011/07/29 2012/07/29 Power Sensor Agilent E9300A MY41498484 2011/08/05 2012/08/05 Power Sensor Agilent E9300A MY41498492 2011/08/05 2012/08/05 SAR Test Report No: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix C Page 5 of 6 Equipment Calibration/Performance Documents: KDB 450824 states that the return-loss and impedance of dipoles should be measured at least annually to ensure dipoles meet specification. Section 1c) states the return loss should not deviate by more than 20% (0.79 dB) of the previuos measurement. Section 1d) states the real or imaginary parts of the impedance should not deviate by more than 5 Ω from the previous measurement. Measurements were made with the dipole against the flat phantom, filled with head or body liquid for the respective frequency. Muscle Simulating Liquid Dipole 835 MHz SN: 4d113 1900 MHz SN: 5d135 Date Measured 2012/03/05 2012/03/05 Measured Return-Loss [dB] -27.304 -21.620 Target Return- Loss [dB] -26.8 -22 Return-Loss Deviation [dB] -0.50 0.38 Measured Real Impedance [Ω] 45.08 44.29 Target Real Impedance [Ω] 48.1 47.3 Real Impedance Deviation [Ω] -3.02 -3.01 Measured Imaginary Impedance [Ω] -5.90 5.62 Target Imaginary Impedance [Ω] -4.1 7.3 Imaginary Impedance Deviation [Ω] -1.8 -1.68 SAR Test Report No: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix C Page 6 of 6 Attached: SAR Probe ES3DV3 Calibration Report 835 MHz Dipole Calibration Report 1900 MHz Dipole Calibration Report
Bluetooth Qualification Test Facility (BQTF) FCC Listed #: A2LA Accredited IC Recognized # 3462B-1 CETECOM Inc. 411 Dixon Landing Road Milpitas, CA 95035 U.S.A. Phone: + 1 (408) 586 6200 Fax: + 1 (408) 586 6299 E-mail: [email protected] http://www.cetecom.com CETECOM Inc. is a Delaware Corporation with Corporation number: 2113686 V3.0 2010-12-30 The BLUETOOTH trademarks are owned by Bluetooth SIG, Inc., U.S.A. and licensed to CETECOM Inc. © Copyright by CETECOM SAR Test Report FOR: Manufacturer: TZ Medical, Inc. Model Name: Aera CT FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Test Report #: SAR_TZMED_001_10001_FCC Date of Report: 2012-03-16 Test Report #: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report : 2012-03-16 Page 2 of 22 V3.0 2010-12-30 This report shall not be reproduced except in full without the written approval of: CETECOM Inc. SAR 411 Dixon Landing Road Milpitas, CA 95035 U.S.A. TABLE OF CONTENTS 1. Assessment ............................................................................................................................ 4 2. Administrative Data ............................................................................................................. 5 2.1. Identification of the Testing Laboratory Issuing the SAR Test Report ............................ 5 2.2. Identification of the Client .................................................................................................... 5 2.3. Identification of the Manufacturer ...................................................................................... 5 3. Equipment under Test (EUT) .............................................................................................. 6 3.1. Specification of the Equipment under Test ......................................................................... 6 3.2. Identification of the Equipment Under Test (EUT) ............................................................ 6 3.3. Identification of Accessory equipment ................................................................................. 6 4. Subject of Investigation ....................................................................................................... 7 4.1. The IEEE Standard C95.1 and the FCC Exposure Criteria.............................................. 7 4.2. Distinction Between Exposed Population, Duration of Exposure and Frequencies ........ 7 4.3. Distinction between Maximum Permissible Exposure and SAR Limits ........................... 8 4.4. SAR Limit ............................................................................................................................... 8 5. The FCC Measurement Procedure and IC Measurement Procedure ............................... 9 5.1. General Requirements ........................................................................................................... 9 5.2. Body-worn and Other Configurations ................................................................................. 9 5.3. Procedure for assessing the peak spatial-average SAR .................................................... 10 5.4. Determination of the largest peak spatial-average SAR .................................................. 12 6. The Measurement System .................................................................................................. 13 6.1. Robot system specification .................................................................................................. 13 6.2. Isotropic E-Field Probe for Dosimetric Measurements ................................................... 14 6.3. Data Acquisition Electronics ............................................................................................... 14 6.4. Phantoms .............................................................................................................................. 14 Test Report #: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report : 2012-03-16 Page 3 of 22 V3.0 2010-12-30 This report shall not be reproduced except in full without the written approval of: CETECOM Inc. SAR 411 Dixon Landing Road Milpitas, CA 95035 U.S.A. 6.5. Interpolation and Extrapolation schemes .......................................................................... 14 7. Uncertainty Assessment ..................................................................................................... 15 7.1. Measurement Uncertainty Budget ..................................................................................... 15 8. Test results summary ......................................................................................................... 16 8.1. Conducted Average Output Power .................................................................................... 16 8.2. Test Positions and Configurations ...................................................................................... 18 8.3. SAR Results for Body .......................................................................................................... 18 8.4. SAR Results Extrapolated to Upper Tolerance Limit ...................................................... 19 8.5. Dipole verification ................................................................................................................ 20 9. References .......................................................................................................................... 21 10. Report History .................................................................................................................... 22 Test Report #: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report : 2012-03-16 Page 4 of 22 V3.0 2010-12-30 This report shall not be reproduced except in full without the written approval of: CETECOM Inc. SAR 411 Dixon Landing Road Milpitas, CA 95035 U.S.A. 1. Assessment The following device was tested against the limits for general popu…
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SAR Test Report No.: SAR_TZMED_001_10001_FCC FCC ID: ZIMTZMR IC ID: 9647Z-TZMR Date of Report: 2012-03-16 Appendix A Plots Page 1 of 11 Plot 1: Date/Time: 2/13/2012 4:09:32 PM Test Laboratory: Cetecom Inc. SAR 1 Lab DUT: TZ Medical; Type: Not Speci…
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| # | Rule Parts | Frequency Range | Power Output | Emission | Tolerance |
|---|---|---|---|---|---|
| 4 | 24E | 1.85 GHz - 1.91 GHz | 1.07 W | 243KG7W | 2.5 ppm |

Ambulatory electrocardiograph monitor with onboard ECG analysis and wireless connection via Wi-Fi and BLE
Equipment Class
DTS - Digital Transmission System
Ambulatory electrocardiograph monitor
Equipment Class
PCT - PCS Licensed Transmitter worn on body