2ABWK-30-30-0002ReWalk P INF

User Guide Argo ™ P Designed for Personal Use Overcoming Mobility Impairment User Guide Page 2 of 66 Important The user of this product has sole responsibility for any malfunction that results from improper use, faulty maintenance, improper repair, unauthorized service, damage, or alteration by anyone other than Argo Medical Technologies. The safety, reliability, and performance of this product can only be assured under the following conditions: The product has been used according to the accompanying operating instructions. All updates, extensions, readjustments, changes, or repairs have been carried out by Argo Medical Technologies' authorized representatives. Document Information User Guide Revision 1, February 2014. Document Number: 60-70-0015. © Copyright 2012-2014 Argo Medical Technologies, Inc. All rights reserved. This User Guide is subject to periodic review, update and revision. No part of this document may be reproduced or transmitted in any form or by any means, electronic or mechanical, for any purpose, without the express written permission of Argo Medical Technologies Ltd. Under the law, reproducing includes translating into another language or format. Every effort has been made to ensure that the information in this manual is accurate. Argo Medical Technologies Ltd. is not responsible for printing or clerical errors. Information in this document is subject to change without notice. Argo Medical Technologies, Inc. reserves the right to change or improve its products and accompanying technical literature without specific notice of changes or improvements. Trademarks and Software Information ReWalk ™ is a registered trademark of Argo Medical Technologies Ltd. All other trademarks are the property of their respective owners. Software Protection As between the parties, Argo Medical Technologies Ltd. retains title to, and ownership of, all proprietary rights with respect to the software contained within its products. The software is protected by United States copyright laws and international treaty provision. Therefore, you must treat the software like any other copyrighted material (e.g. a book or sound recording). Patent pending Notification Regarding Training Warning: Training is mandatory. Use this document as a guide during training and as a reference after training. This manual is not a substitute for training. User Guide Page 3 of 66 Caution: Before using the ReWalk, read this Guide carefully to attain a solid understanding of its functions and operations. Keep this Guide handy so that it can be referred to whenever needed. Follow the operating procedures and usage described in this Guide. Do not modify the device, replace parts (with the exception of the batteries), use non- specified parts, or remove protection devices, as these actions could result in a hazardous situation. PLEASE READ THIS USER GUIDE BE FORE OPERATING THE SY STEM User Guide Page 4 of 66 Israel ◦ Argo Medical Technologies, Ltd. Kochav Yokneam Building, 6th Floor P.O. Box 161 Yokneam Ilit 20692 Phone: +972-4-959-0123 Fax: +972-4-959-0125 United States Office ◦ Argo Medical Technologies, Inc. 33 Locke Drive, 2nd Floor Marlborough, MA 01752 Phone: +01-508 251-1154 Germany Office ◦ Argo Medical Technologies, GmbH Potsdamer Platz 11 107585 Berlin Phone: +49(0)30/25895080 Fax: +49(0)/3025894110 EU Authorized Representative Gerrit van der Veenstraat 84 HS 1077 EL Amsterdam Netherlands Phone: +31(0)20811-0550 Disclaimer Information provided by Argo Medical Technologies is believed to be accurate and reliable. However, Argo Medical Technologies assumes no responsibility for the use of such information, nor for any infringements of patents or other rights of third parties, that may result from its use. Your Dealer’s Contact Information email: [email protected] web: www.rewalk.com User Guide Page 5 of 66 TABLE OF CONTENTS 1. Introduction 6 1.1. ABOUT THIS USER GUIDE ..................................................................................................................... 6 1.2. GLOSSARY AND ABBREVIATIONS ............................................................................................................ 6 2. System Description 7 2.1. INTENDED USE ................................................................................................................................... 7 2.2. INDICATIONS ...................................................................................................................................... 7 2.3. CONTRAINDICATIONS........................................................................................................................... 7 3. Safety 8 3.1. TYPES OF WARNINGS, CAUTIONS AND NOTES .......................................................................................... 8 3.2. GENERAL SAFETY INSTRUCTIONS ............................................................................................................ 9 3.3. SAFETY STANDARDS .......................................................................................................................... 11 3.4. SYMBOLS USED IN THIS GUIDE ............................................................................................................ 11 4. System Components 12 4.1. THE COMMUNICATOR ....................................................................................................................... 13 4.2. THE EXOSKELETON ............................................................................................................................ 16 4.3. THE BACKPACK ................................................................................................................................. 16 5. Moving Into the ReWalk 20 5.1. PREPARATION .................................................................................................................................. 20 5.2. SECURING THE REWALK™- P ......................................................................................…

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Theory of Operation The communication between the ReWalk P Communicator and the ReWalk INF is done via a RF 2.4 GHz link using a proprietary protocol. The protocol is a master-slave protocol, with the ReWalk P Communicator acting as the master and the ReWalk P INF as the slave. After performing built in tests the ReWalk P Communicator sends a Current Mode Request message to the MPB and expects to receive the system current mode. After receiving an answer it illuminates the received mode and starts sending periodic messages every 35 Milliseconds. This message includes the ReWalk P Communicator illuminated mode. If the user selects a new mode, the ReWalk P Communicator will start transmitting the selection but will keep illuminate the mode received from the ReWalk P INF.

Test Report E137190.01 Argo Medical Technologies Ltd. Page 1 of 44 ITL FCCMASVE 1.25 26 March 2003 DATE: 3 March 2014 I.T.L. (PRODUCT TESTING) LTD. FCC Radio Test Report for Argo Medical Technologies Ltd. Equipment under test: ReWalk P INF 30-30-0002 Written by: ____________________________ R. Pinchuck, Documentation Approved by: _____________________________ A. Sharabi, Test Engineer Approved by: _____________________________ I. Raz, EMC Laboratory Manager This report must not be reproduced, except in full, without the written permission of I.T.L. (Product Testing) Ltd. This report relates only to items tested. Test Report E137190.01 Argo Medical Technologies Ltd. Page 2 of 44 ITL FCCMASVE 1.25 26 March 2003 Measurement/Technical Report for Argo Medical Technologies Ltd. Equipment under test: ReWalk P INF 30-30-0002 FCC ID: 2ABWK-30-30-0002 This report concerns: Original Grant: x Class I change: Class II change: Equipment type: Digital Transmission System Limits used: 47CFR15 Section 15.249 (a-b) Measurement procedure used is KDB 558074 D01, April 1, 2013 and ANSI C63.4-2003. Application for Certification Applicant for this device: prepared by: (different from "prepared by") R. Pinchuck Argo Medical Technologies Ltd. ITL (Product Testing) Ltd. 6 th Floor, Kochav Yokneam Building Kfar Bin Nun P.O.B. 161 D.N. Shimshon 99780 Yokneam Ilit, 206292 Israel Israel Tel: +972-8-918-6117 Tel: +972-4-959-0123 Fax: +972-8-915-3101 Fax: +972-4-959-0125 Email: [email protected] Email: Test Report E137190.01 Argo Medical Technologies Ltd. Page 3 of 44 ITL FCCMASVE 1.25 26 March 2003 TABLE OF CONTENTS 1. GENERAL INFORMATION ------------------------------------------------------------------------------- 4 1.1 Administrative Information ................................................................................. 4 1.2 List of Accreditations ......................................................................................... 5 1.3 Product Description ........................................................................................... 6 1.4 Test Methodology .............................................................................................. 6 1.5 Test Facility ....................................................................................................... 6 1.6 Measurement Uncertainty ................................................................................. 6 2. SYSTEM TEST CONFIGURATION --------------------------------------------------------------------- 7 2.1 Justification ........................................................................................................ 7 2.2 EUT Exercise Software ..................................................................................... 7 2.3 Special Accessories .......................................................................................... 7 2.4 Equipment Modifications ................................................................................... 7 2.5 Configuration of Tested System ........................................................................ 7 3. CONDUCTED AND RADIATED MEASUREMENT TEST SET-UP PHOTO ----------------- 8 5. FIELD STRENGTH OF FUNDAMENTAL ------------------------------------------------------------17 5.1 Test Specification ............................................................................................ 17 5.2 Test Procedure ................................................................................................ 17 5.3 Measured Data ................................................................................................ 17 5.4 Test Instrumentation Used, Field Strength of Fundamental ........................... 22 6. RADIATED EMISSION, 9 KHZ – 30 MHZ -----------------------------------------------------------23 6.1 Test Specification ............................................................................................ 23 6.2 Test Procedure ................................................................................................ 23 6.3 Measured Data ................................................................................................ 23 6.4 Test Instrumentation Used, Radiated Measurements ..................................... 24 6.5 Field Strength Calculation ............................................................................... 25 7. SPURIOUS RADIATED EMISSION 30 MHZ - 25GHZ --------------------------------------------26 7.1 Test Specification ............................................................................................ 26 7.2 Measured Data ................................................................................................ 27 7.3 Test Instrumentation Used .............................................................................. 32 7.4 Field Strength Calculation ............................................................................... 33 8. ANTENNA GAIN/INFORMATION ----------------------------------------------------------------------34 9. R.F EXPOSURE/SAFETY --------------------------------------------------------------------------------35 10. APPENDIX A - CORRECTION FACTORS ----------------------------------------------------------36 10.1 Correction factors for CABLE ......................................................................... 36 10.2 Correction factors for CABLE ......................................................................... 37 10.3 Correction factors for CABLE ......................................................................... 38 8.4 Correction factors for LOG PERIODIC ANTENNA ........................................ 39 10.5 Correction factors for LOG PERIODIC ANTENNA ........................................ 40 10.6 Correction factors for BICONICAL ANTENNA ............................................... 41 10.7 Correction factors for Double-Ridged Waveguide Horn .................................. 42 10.8 Correction factors for Horn Antenna …

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