LF535373537

CONTROLLER3537 for InterStim ® Therapy Clinician Programming Guide ! USA Rx only Filename Date Time UC2001xxxx EN 4.625 x 6 inches (117 mm x 152 mm) Medtronic Confidential PTMClinPrgmManual.xsl - PTMClinPrgmTemplate.fm Template version: 08-08-2011 M943580A002 Rev X 2012-09 Filename Date Time UC2001xxxx EN 4.625 x 6 inches (117 mm x 152 mm) Medtronic Confidential PTMClinPrgmManual.xsl - PTMClinPrgmTemplate.fm Template version: 08-08-2011 M943580A002 Rev X 2012-09 Explanation of symbols on product or package labeling Refer to the appropriate product for symbols that apply. Consult instructions for use Manufacturer XXX °F XX °C -XX °F -XX °C Temperature limitation Serial number Conformité Européenne (European Conformity). This symbol means that the device fully complies with MDD 93/42//EEC (NB 0123) and R&TTE Directive 1999/5/EC. EC REP Authorized representative in the European community ! USA For USA audiences only IEC 60601-1/EN60601-1, Type BF equipment Non-ionizing electromagnetic radiation System meets the applicable Canadian (CAN/CSAC22.2 No. 60601-1) electrical safety standard requirements. Do not dispose of this product in the unsorted municipal waste stream. Dispose of this product according to local regulations. See http://recycling.medtronic.com for instructions on proper disposal of this product. Chinese Standard (SJ/T11364-2006) Logo: Electronic Information Products Pollution Control Symbol. (The date in this logo means the environmental protection use period of the product.) 3537 2012-09 English 3 Filename Date Time UC2001xxxx EN 4.625 x 6 inches (117 mm x 152 mm) Medtronic Confidential PTMClinPrgmManual.xsl - PTMClinPrgmTemplate.fm Template version: 08-08-2011 M943580A002 Rev X 2012-09 Medtronic ® , and InterStim ® are trademarks of Medtronic, Inc., registered in the U.S. and other countries. ! USA FCC Information The following is communications regulation information on the Model 3537 Personal Therapy Manager. FCC ID: LF53537 This device complies with Part 15 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. IMPORTANT: Changes or modifications to this product not authorized by Medtronic, Inc., could void the FCC Certification and negate your authority to operate this product. This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device. 4 English 3537 2012-09 Filename Date Time UC2001xxxx EN 4.625 x 6 inches (117 mm x 152 mm) Medtronic Confidential PTMClinPrgmManual.xsl - PTMClinPrgmTemplate.fm Template version: 08-08-2011 M943580A002 Rev X 2012-09 Table of contents Description 7 Package contents 7 About this manual 7 Instructions for use 8 Setting up the controller 8 Pairing the controller to the external neurostimulator 11 Pairing a new controller to an external neurostimulator 11 Pairing a previously used controller to an external neurostimulator 14 Unlocking and locking the controller 19 Unlocking the controller 19 Locking the controller 21 Turning stimulation on or off 22 Turning stimulation on 22 Turning stimulation off 23 Adjusting stimulation parameters using the Model 3575 Test Stimulation Cable 25 Increasing and decreasing amplitude on the Home screen 25 Adjusting advanced parameters 27 Adjusting stimulation parameters for the Model 3057 Test Stimulation Lead(s) 30 Increasing and decreasing amplitude on the Home screen 30 Changing the active lead (if two leads were placed) 32 Adjusting advanced parameters 33 Refer to the indications sheet for indications and related information. Refer to the appropriate information for prescribers booklet for contraindications, warnings, precautions, adverse events summary, individualization of treatment, patient selection, use in specific populations, resterilization, and component disposal. Refer to System Eligibility, Battery Longevity, Specifications reference manual for neurostimulator selection, battery longevity calculations, and specific neurostimulator specifications. ! USA Refer to the clinical summary booklet for information on the clinical study results of the neurostimulation system and individualization of treatment. 3537 2012-09 English 5 Filename Date Time UC2001xxxx EN 4.625 x 6 inches (117 mm x 152 mm) Medtronic Confidential PTMClinPrgmManual.xsl - PTMClinPrgmTemplate.fm Template version: 08-08-2011 M943580A002 Rev X 2012-09 Adjusting stimulation parameters for the Model 3093 or Model 3889 Tined Lead 37 Adjusting advanced parameters 37 Increasing and decreasing amplitude on the Home screen 41 Usage Log 42 Reset Therapy 44 Changing preferences 46 Changing the vibration settings 46 Changing the brightness of the controller display 48 Changing the time 49 Changing the date 50 Changing the number format 51 Changing the language 52 Viewing information about the controller and the external neurostimulator 54 Checking and replacing batteries 55 Checking the external neurostimulator and controller batteries 55 Replacing the controller batteries 58 Labeling the controller 59 Troubleshooting 59 Troubleshooting reference guide 60 Device specifications 65 Device care and storage 65 6 English 3537 2012-09 Filename Date Time UC2001xxxx EN 4.625 x 6 inches (117 mm x 152 mm) Medtronic Confidential PTMClinPrgmManual.xsl - PTMClinPrgmTemplate.fm Template version: 08-08-2011 M943580A002 Rev X 2012-09 Description The Medtronic Model 3537 Controller is a hand-held device intended for use with the Medtronic Model 3531 External Neurostimulator. The clinician uses the controller to program settings for the patient. The patient uses the controller to perform the following tasks as directed by the clinician: ▪ Adjust amplitude ▪ Switc…

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CONTROLLER 3537 Patient Programming Manual for Test Stimulation ! USA Rx only 0123 Filename Date Time UC200xxxxxx EN 4.625′′ x 6.0′′ inches (117 mm x 152 mm) Medtronic Confidential PPManual.xsl - PatientProgrammerTemplate.fm Version: 01-18-2012 M943578A001 Rev X 2013-3 Medtronic ® and InterStim ® are trademarks of Medtronic, Inc., registered in the U.S. and other countries. ! USA FCC Information The following is communications regulation information on the Model 3537 Controller. FCC ID: LF597745 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. IMPORTANT: Changes or modifications to this product not authorized by Medtronic, Inc., could void the FCC Certification and negate your authority to operate this product. This device complies with Industry Canada license- exempt RSS standard(s). Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device. Filename Date Time UC200xxxxxx EN 4.625′′ x 6.0′′ inches (117 mm x 152 mm) Medtronic Confidential PPManual.xsl - PatientProgrammerTemplate.fm Version: 01-18-2012 M943578A001 Rev X 2013-3 Label symbols Explanation of symbols on products and packaging. Refer to the appropriate product to see symbols that apply. Consult instructions for use Manufacturer XXX °F XX °C -XX °F -XX °C Temperature limitation Serial number Conformité Européenne (European Conformity). This symbol means that the device fully complies with MDD 93/42/EEC (NB 0123) and R&TTE Directive 1999/5/ EC. EC REP Authorized representative in the European community ! USA For USA audiences only IEC 60601-1/EN60601-1, Type BF Equipment Non-ionizing electromagnetic radiation 3537 2013-3 English Filename Date Time UC200xxxxxx EN 4.625′′ x 6.0′′ inches (117 mm x 152 mm) Medtronic Confidential PPManual.xsl - PatientProgrammerTemplate.fm Version: 01-18-2012 M943578A001 Rev X 2013-3 3 Label symbols System meets the applicable (CAN/CSA- C22.2 No. 60601-1) electrical safety standard requirements. Do not dispose of this product in the unsorted municipal waste stream. Dispose of this product according to local regulations. See http://recycling.medtronic.com for instructions on proper disposal of this product. Chinese Standard (SJ/T11364-2006) Logo: Electronic Information Products Pollution Control Symbol. (The date in this logo means the environmental protection use period of the product.) English 3537 2013-3 Filename Date Time UC200xxxxxx EN 4.625′′ x 6.0′′ inches (117 mm x 152 mm) Medtronic Confidential PPManual.xsl - PatientProgrammerTemplate.fm Version: 01-18-2012 M943578A001 Rev X 2013-3 4 Label symbols Table of contents Label Symbols 3 Glossary 7 1 Introduction 10 How to use this manual 10 Patient guides 11 2 Using your controller 14 How your controller works 14 Controller screen and keys 15 Unlocking and locking your controller 17 Unlocking your controller 17 Locking your controller 21 Turning your stimulation on or off 22 Turning your stimulation on 23 Turning your stimulation off 25 Adjusting stimulation 27 Switching stimulation sides (if your clinician placed two leads) 28 Changing programs (if applicable) 31 3537 2013-3 English Filename Date Time UC200xxxxxx EN 4.625′′ x 6.0′′ inches (117 mm x 152 mm) Medtronic Confidential PPManual.xsl - PatientProgrammerTemplate.fm Version: 01-18-2012 M943578A001 Rev X 2013-3 5 Table of contents Home screen 34 Checking and replacing batteries 38 Checking the batteries (external neurostimulator and controller) 38 Replacing the batteries (controller only) 45 Using the carrying case 46 Always carry your controller 47 3 Troubleshooting 50 Controller screens 50 Warning screens 51 Alert screens 56 Notification screens 61 Possible problems and solutions 64 4 Maintenance and assistance 74 Cleaning and care 74 Safety and technical checks 75 Battery and controller disposal 75 Declaration of conformity 75 Specifications 76 Assistance for the controller 76 Index 78 English 3537 Filename Date Time UC200xxxxxx EN 4.625′′ x 6.0′′ inches (117 mm x 152 mm) Medtronic Confidential PPManual.xsl - PatientProgrammerTemplate.fm Version: 01-18-2012 M943578A001 Rev X 2013-3 6 Table of contents Glossary Amplitude - The strength or intensity of an electrical pulse. Caution - A statement describing actions that could result in damage to or improper functioning of a device. Clinician - A healthcare professional such as a doctor or nurse. Controller - A hand-held device that allows you to turn your neurostimulator on and off and check your neurostimulator battery. It is also used to adjust some of the stimulation settings. External neurostimulator (ENS) - See Neurostimulator. Lead - A thin wire with protective coating that has metal electrodes on one end and a connector on the other. Neurostimulator - The power source of a neurostimulation system. It contains the battery and electronics that control the stimulation. 3537 2013-3 English Filename Date Time UC200xxxxxx EN 4.625′′ x 6.0′′ inches (117 mm x 152 mm) Medtronic Confidential PPManual.xsl - PatientProgrammerTemplate.fm Version: 01-18-2012 M943578A001 Rev X 2013-3 7 Glossary Precaution - See Caution. Program - A specific combination of stimulation settings assigned to deliver therapy to a specific site. Settings - See Stimulation settings. Stimulation - The delivery of electrical pulses to a specific site. Stimulation settings - Refers to all the features assembled to define the stimulation you feel. The clinician programs all stimulation. You can adjust some stimulation settings within clinician-defined limits. Test stimulation - A postoperative multiday trial period of a patient’s reaction to stimulation using an external neurostimulator and implant…

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Northwest EMC TCB Compliance Opinion Rev. 7/1/10 MDTR0160 Information about the Applicant Grantee (Company Name) Medtronic Inc. FCC Contact Person Charles Farlow Address 8200 Coral Sea Street NE City, State, Zip Mounds View, MN 55112 Job Number MDTR0160 Model 3537 FCC ID LF53735 Agent Anne Coldwell Approval Type Original Equipment Class DSS Part 15, Spread Spectrum Transmitter Rule Part Bluetooth Overview This application is for original approval of Medtronic Inc.'s Interstim PTM3 model 3537 with Bluetooth radio transceiver. Confidentiality requested for allowed files. Request is properly addressed and referenced. Short term confidentiality requested. Recommendation All items have been resolved and completed to my satisfaction; therefore I recommend this application for approval. Signature Dave Tolman, TCB Committee 6/5/2012

PTM Interstim Model 3537 Front View PTM Interstim Model 3537 Back View PTM Interstim Model 3537 Bottom View PTM Interstim Model 3537 Top View PTM Interstim Model 3537 Left Side View PTM Interstim Model 3537 Right Side View

Rx only FCC ID: LF53537 IC:3408D-MPPGR6 3537 M947531A002 MR CAD MODEL: EMPTY A DOCUMENT RELEASE11-0272601JUL11CEPDL B CHANGED NOTES 3 AND 411-0547117DEC11CEPCF C CHANGED NOTE 1112-0188101MAY12CEPCF TITLE DEVICE ASSEMBLY - PTM3, 8836 . DATE DO NOT SCALE PRINT DIMENSIONS ARE IN INCHES 01APR10 DRAFTING THE CAD DATA FOR THIS PART NUMBER CAN BE MADE AVAILABLE UPON REQUEST C. PETERS ENGINEERING D. LEE X.X .1 X.XX .01 X.XXX .005 X.XXXX .0005 ANGLES 1.0 D E S I G N D O C U M E N T TYPE FIRST DESIGNED FOR - MODELNEXT ASSY -- SIZE DOCUMENT NUMBERREV SHEET D M937021AC 1 OF 2 NOTES 1 ASSEMBLY SHALL MEET ALL REQUIREMENTS CONTAINED IN THE RELATED ENGINEERING BILL OF DOCUMENTS, BILL OF MATERIALS AND SPECIFICATIONS. 2 PRESS-FIT BATTERY CONTACT INTO CASE HALF BOTTOM. BATTERY CONTACT MUST BE FULLY SEATED AGAINST STOPS IN CASE HALF BOTTOM. 3 TIGHTEN SCREWS F/N 9 TO 2.00.05 LB-IN TORQUE. 4 TIGHTEN SCREWS F/N 10 TO 1.50.05 LB-IN TORQUE. 5 CLEAN DOME CONTACT AREAS ON PWB WITH ISOPROPYL ALCOHOL PRIOR TO ASSEMBLING DOME SHEET TO PWB. REMOVE DOME SHEET FROM RELEASE LINER AND LOCATE ON PCB WITH PROVIDED TOOLING HOLES. 6 LCD FLEX TAIL AND VIBRATOR MOTOR TO BE CONNECTED TO RESPECTIVE RECEPTICAL ON PCB. 7 LABELS TO BE LOCATED WITHIN SILK SCREEN OUTLINES ON PCB. ORIENTATION TO MATCH SILK SCREEN POLAIRITY INDICATORS 8 SERIAL NUMBER / BARCODE LABEL TO BE ADHERED TO RECESS IN CASE BOTTOM ASSEMBLY. 9 LABEL TO BE APPLIED TO RECESS IN BATTERY DOOR. ORIENTATION TO BE RIGHT READING, AND SAME DIRECTION AS LOGO ON ACCENT BAND. 10 REMOVE ADHESIVE LINER ON ACCENT BAND BEFORE INSTALLING. ACCENT BAND TO BE FULLY SEATED ON CASE HALF BOTTOM. 11 A PROTECTIVE FILM SHALL BE PLACED OVER LCD LENS. SUPPLIER LABELS ON THE PROTECTIVE FILM ARE ALLOWED, BUT CANNOT BE PLACED OVER DISPLAY AREA. 12 UPON APPROVAL BY MEDTRONIC, INC. OF THE INITIAL DESIGN, ANY PROCESS CHANGES, DESIGN CHANGES OR DEVIATIONS CONSIDERED BY THE MANUFACTURER SHALL BE SUBMITTED TO MEDTRONIC, INC. IN WRITING FOR REVIEW. IF CHANGES ARE SUBMITTED FOR APPROVAL, THE INFORMATION SUBMITTED SHALL INCLUDE A COMPLETE DESCRIPTION OF THE CHANGE AND THE EFFECT THE CHANGE WILL HAVE ON ALL CHARACTERISTICS OF THE DEVICE/MATERIAL. UPON REQUEST, THE MANUFACTURER SHALL SUBMIT SAMPLES OF THE PROPOSED DEVICE/MATERIAL FOR THE EVALUATION AND APPROVAL BY MEDTRONIC, INC. 13 CLEAN MATING AREA ON CASE HALF BOTTOM CORRESPONDING TO ADHESIVE AREA ON ACCENT BAND WITH ISOPROPYL ALCOHOL PRIOR TO ASSEMBLY. ORIENT ARROWS AS SHOWN SEE SHEET 2 SEE SHEET 2 DOCUMENT NUMBERREV SHEET M937021AC 2 OF 2 VIEW SHOWN WITH F/N 18 REMOVED SCALE 4.000 STOP IN CASE HALF BOTTOM 2 PLACES

PTM Interstim Model 3537 PCBA Front View PTM Interstim Model 3537 PCBA Back View Bluetooth PCB Antenna Bluetooth Module PTM Interstim Model 3537 Internal View of LCD with Flex Circuit

Antenna Information for PTM3 Model 3537 The Bluetooth antenna used in the PTM3 Model 3537 is a monopole antenna incorporated into the Printed Circuit Board. Therefore the specific antenna will be used in all cases by default. No replacement of the antenna is required. The Bluetooth antenna used in the PTM3 Model 3537 is a part of the PCB and has no model number. It is manufactured by Medtronic, Inc and is a planar monopole antenna. The gain for the PTM3 Bluetooth antenna is -1.37 dBi. Bluetooth Antenna

Compliance with 47 CFR 15.247(i) “Systems operating under the provisions of this section shall be operated in a manner that ensures that the public is not exposed to radio frequency energy levels in excess of the Commission's guidelines. See § 1.1307(b)(1) of this chapter.” It is possible that some device configurations are less than 20 cm from the user. Therefore, the device can be considered a portable transmitter per 47 CFR 2.1093(b). The maximum antenna gain is -1.37 dBi. The maximum peak conducted output power is 2.79 mW. The maximum peak radiated power is 2.04 mW (EIRP) for FCC ID: LF53537. The transmit frequency is in the 2400 – 2483.5 MHz band, therefore the EUT does not require routine SAR evaluation because it falls below the low power threshold of 60/f(GHz) mW. Please see this excerpt from KDB 447498D01 Mobile Portable RF Exposure v04, item 2)(a)(i): “A device may be used in portable exposure conditions with no restrictions on host platforms when either the source-based time-averaged output power is ≤ 60/f(GHz) mW or all measured 1-g SAR are < 0.4 W/kg.” The applicant’s radio, FCC ID: LF53537, is compliant with the requirements of 15.247(i).

Medtronic Inc. Interstim Model 3537 (PTM) Report #: MDTR0153 Report Prepared By Northwest EMC Inc. NORTHWEST EMC – (888) 364-2378 – www.nwemc.com California – Minnesota – Oregon – New York – Washington 22975 NW Evergreen Parkway Suite 400 Hillsboro, Oregon 97124 Certificate of Test Last Date of Test: April 9, 2012 Medtronic Inc. Model: Interstim Model 3537 (PTM) Emissions Test Description Specification Test Method Pass/Fail Channel Spacing FCC 15.247:2012 ANSI C63.10:2009 Pass Dwell Time FCC 15.247:2012 ANSI C63.10:2009 Pass Number of Hopping Frequencies FCC 15.247:2012 ANSI C63.10:2009 Pass Occupied Bandwidth FCC 15.247:2012 ANSI C63.10:2009 Pass Output Power FCC 15.247:2012 ANSI C63.10:2009 Pass Band Edge Compliance FCC 15.247:2012 ANSI C63.10:2009 Pass Band Edge - Hopping Mode FCC 15.247:2012 ANSI C63.10:2009 Pass Spurious Conducted Emissions FCC 15.247:2012 ANSI C63.10:2009 Pass Power Spectral Density FCC 15.247:2012 ANSI C63.10:2009 Pass Duty Cycle FCC 15.247:2012 ANSI C63.10:2009 Pass Spurious Radiated Emissions FCC 15.247:2012 ANSI C63.10:2009 Pass Deviations From Test Standards None Approved By: Tim O'Shea, Operations Manager NVLAP Lab Code: 200881-0 Test Facility The measurement facility used to collect the data is located at: Northwest EMC, Inc. 9349 W Broadway Ave. Brooklyn Park, MN 55445 Phone: (763) 425-2281 Fax: (763) 424-3469 This site has been fully described in a report filed with and accepted by the FCC (Federal Communications Commission) and Industry Canada (Site filing #2834E-1). This report must not be used to claim product certification, approval, or endorsement by NVLAP, NIST, or any agency of the federal government of the United States of America. Product compliance is the responsibility of the client, therefore the tests and equipment modes of operation represented in this report were agreed upon by the client, prior to testing. This Report may only be duplicated in its entirety. The results of this test pertain only to the sample(s) tested. The specific description is noted in each of the individual sections of the test report supporting this certificate of test. Revision History Revision 09/01/11 Revision Number Description Date Page Number 00 None Accreditations and Authorizations Revision 02/21/2012 United States FCC - Designated by the FCC as a Telecommunications Certification Body (TCB). Certification chambers, Open Area Test Sites, and conducted measurement facilities are listed with the FCC. A2LA - Accredited by A2LA to ISO / IEC Guide 65 as a product certifier. This allows Northwest EMC to certify transmitters to FCC and IC specifications. NVLAP - Each laboratory is accredited by NVLAP to ISO 17025. The scope includes radio, ITE, and medical standards from around the world. See: http://www.nwemc.com/accreditations/ Canada IC - Recognized by Industry Canada as a Certification Body (CB). Certification chambers and Open Area Test Sites are filed with IC. European Union European Commission – Validated by the European Commission as a Conformity Assessment Body (CAB) under the EMC directive and as a Notified Body under the R&TTE Directive. Australia/New Zealand ACMA - Recognized by ACMA as a CAB for the acceptance of test data. Korea KCC / RRA - Recognized by KCC’s RRA as a CAB for the acceptance of test data. Japan VCCI - Associate Member of the VCCI. Conducted and radiated measurement facilities are registered. Taiwan BSMI – Recognized by BSMI as a CAB for the acceptance of test data. NCC - Recognized by NCC as a CAB for the acceptance of test data. Singapore IDA – Recognized by IDA as a CAB for the acceptance of test data. Hong Kong OFTA – Recognized by OFTA as a CAB for the acceptance of test data. Vietnam MIC – Recognized by MIC as a CAB for the acceptance of test data. Russia GOST – Accredited by Certinform VNIINMASH, CERTINFO, SAMTES, and Federal CHEC to perform EMC and Hygienic testing for Information Technology products to GOST standards. Locations Revision 2/23/12 Oregon Labs EV01-EV12 22975 NW Evergreen Pkwy, #400 Hillsboro, OR 97124 (503) 844-4066 California Labs OC01-OC13 41 Tesla Irvine, CA 92618 (949) 861-8918 New York Labs WA01-WA04 4939 Jordan Rd. Elbridge, NY 13060 (315) 685-0796 Minnesota Labs MN01-MN08 9349 W Broadway Ave. Brooklyn Park, MN 55445 (763) 425-2281 Washington Labs SU01-SU07 14128 339 th Ave. SE Sultan, WA 98294 (360) 793-8675 VCCI C-1071, R-1025, G-84, C-2687, T-1658, R-2318 R-1943, G-85, C-2766, T-1659, G-548 R-3125, G-86, G-141, C-3464, T-1634 R-871, G-83, C-3265, T-1511 Industry Canada 2834D-1, 2834D-2 2834B-1, 2834B-2, 2834B-3 2834E-1 2834C-1 Product Description Revision 09/01/11 Client and Equipment Under Test (EUT) Information Company Name: Medtronic Inc. Address: 710 Medtronic Parkway, LS250 City, State, Zip: Fridley, MN 55432 Test Requested By: Paul Wood Model: Interstim Model 3537 (PTM) First Date of Test: April 09, 2012 Last Date of Test: April 09, 2012 Receipt Date of Samples: April 09, 2012 Equipment Design Stage: Production Equipment Condition: No Damage Information Provided by the Party Requesting the Test Functional Description of the EUT (Equipment Under Test): Bluetooth radio installed in Interstim medical device. Testing Objective: To demonstrate compliance to FCC 15.247 requirements. Configurations Revision 09/01/11 Configuration 1 MDTR0153 Software/Firmware Running during test Description Version ptm_ptm3_emi_emc_app_bt_telm_1_2.hex 2.0 EUT Description Manufacturer Model/Part Number Serial Number Interstim PTM3 Medtronic Inc. 3537 NLD001577N Peripherals in test setup boundary Description Manufacturer Model/Part Number Serial Number Laptop Dell Precision M4400 6356184841 Laptop Supply Dell DA130PE1-00 CN-OJU012-48661-9CS-2ZK1-A03 Cables Cable Type Shield Length (m) Ferrite Connection 1 Connection 2 SMA to L Coax Yes 0.3m No Interstim PTM3 Measurement Cable AC Power No 1.94m No Laptop Supply AC Power DC Power No 1.76m Yes Laptop Laptop Supply USB to PTM No 2.46m No Laptop Interstim PTM3 PA = Cable is permanent…

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Channel Spacing XMit 2012.04.06 NORTHWEST Channel Spacing PsaTx 2012.01.25 EMC Direct 003.JPG Direct 001.JPG Channel Spacing Channel Spacing XMit 2012.04.06 NORTHWEST Channel Spacing PsaTx 2012.01.25 EMC Direct 002.JPG Channel Spacing Dwell Time XMit 2012.04.06 NORTHWEST Dwell Time PsaTx 2012.01.25 EMC Direct 003.JPG Direct 001.JPG Dwell Time Dwell Time XMit 2012.04.06 NORTHWEST Dwell Time PsaTx 2012.01.25 EMC Direct 002.JPG Dwell Time Number of Hopping Frequencies XMit 2012.04.06 NORTHWEST Number of Hopping F PsaTx 2012.01.25 EMC Direct 003.JPG Direct 001.JPG Number of Hopping Frequencies Number of Hopping Frequencies XMit 2012.04.06 NORTHWEST Number of Hopping F PsaTx 2012.01.25 EMC Direct 002.JPG Number of Hopping Frequencies Occupied Bandwidth XMit 2012.04.06 NORTHWEST Occupied Bandwidth PsaTx 2012.01.25 EMC Direct 003.JPG Direct 001.JPG Occupied Bandwidth Occupied Bandwidth XMit 2012.04.06 NORTHWEST Occupied Bandwidth PsaTx 2012.01.25 EMC Direct 002.JPG Occupied Bandwidth Output Power XMit 2012.04.06 NORTHWEST Output Power PsaTx 2012.01.25 EMC Direct 003.JPG Direct 001.JPG Output Power Output Power XMit 2012.04.06 NORTHWEST Output Power PsaTx 2012.01.25 EMC Direct 002.JPG Output Power Band Edge Compliance XMit 2012.04.06 NORTHWEST Band Edge Complian PsaTx 2012.01.25 EMC Direct 003.JPG Direct 001.JPG Band Edge Compliance Band Edge Compliance XMit 2012.04.06 NORTHWEST Band Edge Complian PsaTx 2012.01.25 EMC Direct 002.JPG Band Edge Compliance Band Edge Compliance XMit 2012.04.06 NORTHWEST Band Edge Complian PsaTx 2012.01.25 EMC Direct 003.JPG Direct 001.JPG Band Edge Compliance Band Edge Compliance XMit 2012.04.06 NORTHWEST Band Edge Complian PsaTx 2012.01.25 EMC Direct 002.JPG Band Edge Compliance Spurious Conducted Emissions XMit 2012.04.06 NORTHWEST Spurious Conducted PsaTx 2012.01.25 EMC Direct 003.JPG Direct 001.JPG Spurious Conducted Emissions Spurious Conducted Emissions XMit 2012.04.06 NORTHWEST Spurious Conducted PsaTx 2012.01.25 EMC Direct 002.JPG Spurious Conducted Emissions Power Spectral Density XMit 2012.04.06 NORTHWEST Power Spectral Densi PsaTx 2012.01.25 EMC Direct 003.JPG Direct 001.JPG Power Spectral Density Power Spectral Density XMit 2012.04.06 NORTHWEST Power Spectral Densi PsaTx 2012.01.25 EMC Direct 002.JPG Power Spectral Density Duty Cycle XMit 2012.04.06 NORTHWEST Duty Cycle PsaTx 2012.01.25 EMC Direct 001.JPG Direct 002.JPG Duty Cycle Duty Cycle XMit 2012.04.06 NORTHWEST Duty Cycle PsaTx 2012.01.25 EMC Direct 003.JPG Duty Cycle photo SE 04.JPG SE 01.JPG Spurious Radiated Emissions PSA-ESCI 2012.03.23 photo SE 02.JPG SE 03.JPG Spurious Radiated Emissions PSA-ESCI 2012.03.23