About this Manual P/N: 01.54.459103 Version 1.1 MPN: 01.54.459103011 Release Date: Mar. 2022 © Copyright EDAN INSTRUMENTS, INC. 2022. All rights reserved. Statement This manual will help you understand the operation and maintenance of the product better. It is reminded that the product shall be used strictly complying with this manual. User's operation failing to comply with this manual may result in malfunction or accident for which EDAN INSTRUMENTS, INC. (hereinafter called EDAN) cannot be held liable.
personal injury or death. CAUTION A CAUTION label advises against actions or situations that could damage equipment, produce inaccurate data, or invalidate a procedure. NOTE A NOTE provides useful information regarding a function or a procedure.
PA Series Biofeedback and Stimulation System User Manual Safety Guidance Table of Content Chapter 1 Safety Guidance ...................................................................................................... 3 1.1 Intended Use/Indications for Use ........................................................................................................ 3 1.2 Contraindications...........................................................................................................................
PA Series Biofeedback and Stimulation System User Manual Safety Guidance 5.7 Database ............................................................................................................................................ 43 5.7.1 Patient Information.............................................................................................................. 44 5.7.2 Patient Record .....................................................................................................................
PA Series Biofeedback and Stimulation System User Manual Safety Guidance Chapter 1 Safety Guidance CAUTION Federal (U.S.) Law restricts this device to sale by or on the order of a physician. NOTE: 1 To ensure proper running of the device and safety of the operator and patient, read through this chapter before using the device. 2 This user manual is written to cover the maximum configuration.
PA Series Biofeedback and Stimulation System User Manual Safety Guidance 4 SHOCK HAZARD–Do not attempt to connect or disconnect a power cord with wet hands. Make sure that your hands are clean and dry before touching a power cord. 5 SHOCK HAZARD - The power receptacle must be a three-wire grounded outlet. Never try to adapt the three-prong plug to fit a two-slot outlet. A hospital grade outlet is required.
PA Series Biofeedback and Stimulation System User Manual Safety Guidance supplying the system. 14 Multiple portable socket-outlets shall not be placed on the floor. An additional multiple portable socket-outlet or extension cord shall not be connected to the system. 15 Only accessories supplied by the manufacturer can be used. 16 Do not connect any equipment or accessories that are not approved by the manufacturer or that are not IEC/EN 60601-1 approved to the device.
PA Series Biofeedback and Stimulation System User Manual Safety Guidance 28 Please do not plug a random USB flash disk into the device, please use a specialized USB flash disk without virus. 29 Do not apply the device simultaneously with other PATIENT-connected equipment, such as, a cardiac pacemaker or other electrical stimulators, on the same patient. 30 Operation in close proximity (e.g.1m) to a shortwave or microwave may produce instability in the stimulation output.
PA Series Biofeedback and Stimulation System User Manual Safety Guidance 45 Do not use with diminished mental capacity or physical competence limiting the use of the device. 46 Please do not apply stimulation in below situations: a. after bleeding or fracture; b. muscle contraction during surgery; c. during period or pregnancy; d. Skin numbness. 47 Electrode placement and stimulation settings should be operated by qualified personnel.
PA Series Biofeedback and Stimulation System User Manual Safety Guidance 61 Do not heat or throw the lithium battery into a fire. 62 Do not immerse, throw or wet the lithium battery in water, beverages or other liquids.
PA Series Biofeedback and Stimulation System User Manual 2 3 4 5 6 7 8 9 Safety Guidance Keep the environment clean. Make the device far from corrosive medicine, dust area, high-temperature and humid environment. Avoid vibration. Do not move it with the power cord connected. Do not operate the device if it is damp or wet because of condensation or spills. Avoid using the device immediately after moving it from a cold environment to a warm, humid location.
PA Series Biofeedback and Stimulation System User Manual Safety Guidance FCC Statement This device complies with Part 15 of the FCC rules. Operation is subject to the following two conditions: 1) this device may not cause harmful interference, and 2) this device must accept any interference received, including interference that may cause undesired operation. Note: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules.
PA Series Biofeedback and Stimulation System User Manual Safety Guidance 1.4 Definitions and Symbols No.
PA Series Biofeedback and Stimulation System User Manual Safety Guidance Refer to instruction manual/booklet 16 (Background: Blue; Symbol: White) No pushing 17 (Background: White; Symbol: Black; Outline: Red) 18 This way up 19 Fragile, handle with care 20 Keep away from rain 21 Stacking limit by number 23 Do not roll 24 Non-ionizing electromagnetic radiation 25 Adjust Intensity 26 Type BF applied part 27 CH1-CH4 28 CH-P Channel Interface Stress Probe Interface 29 Do not reuse 30
PA Series Biofeedback and Stimulation System User Manual NOTE: 1 The user manual is printed in black and white.
PA Series Biofeedback and Stimulation System User Manual Introduction Chapter 2 Introduction NOTE: The user manual introduces PA4 as an example. You may not have all of these features, depending on the configuration purchased. The pictures and interfaces provided in this manual are for reference only. This device is used with an all-in-one computer and a trolley. For details of the trolley, please refer to the PA trolley installation guide.
PA Series Biofeedback and Stimulation System User Manual Introduction 2.
PA Series Biofeedback and Stimulation System User Manual Introduction 14 13 Figure 2-3 Bottom 1 Touchscreen 2 AC indicator and charge indicator 3 Control knobs 4 Channel interface 5 Scanner 6 Power switch 7 Finger Unlocking 8 Power interface 9 Network Interface 10 USB interface 11 Type-C interface 12 SD card slot 13 Supporting bracket 14 Battery compartment 2.1.
PA Series Biofeedback and Stimulation System User Manual Name Model Pelvic Floor Intracavit y Sensor Pelvic Floor Intracavit y Sensor SV2 SV1 Adhesive Electrode s SK1 Vagina Stress Probe PV Specification Intracavity sensor, which is applied in the vagina and it is reusable Intracavity sensor, which is applied in the vagina and it is disposable. Adhesive electrodes, which are applied on the skin and they are disposable Intracavity stress probe, which is applied in the vagina and it is reusable.
PA Series Biofeedback and Stimulation System User Manual Introduction reusable vagina sensor, pull it out and store it after cleaning and disinfection. Attentions： 1. The reusable vagina sensor is restricted to a single patient, do not cross use it. 2. The disposable vagina sensor is for single use only, do not reuse it. 3. Please do not plug or unplug the sensor during the operation of the host. 4. The device that the 60601-1:2005/A1:2012. sensor connects to has to conform to IEC 5.
PA Series Biofeedback and Stimulation System User Manual Introduction 1. Open the package and connect the stress probe to the host with the sensor cable. 2. Cover the stress probe with a condom and insert the stress probe into the vagina till the groove of the silicon tail, i.e. the location indicated by the red line in below picture. Select an assessment protocol or treatment plan and start it. 3.
PA Series Biofeedback and Stimulation System User Manual Introduction 2.3.3 Charging the Battery 1. Load the battery into the device and connect the device to the mains power. 2. When the battery is being charged, the charge indicator lights up. When the battery is fully charged, the charge indicator is off and the battery power indicator is filled. NOTE: EDAN recommends to charge the battery when the device is switched off so as to improve the charging efficiency and save charging time. 2.3.
PA Series Biofeedback and Stimulation System User Manual Introduction the battery may have failed, check the battery performance. Please refer to Step 1~Step 3 in section 2.3.4, and record the running time of the battery, which reflects the battery performance. If the running time is obviously less than the specified time in the specification, the battery may have reached its service life or malfunctioned, please change the battery or contact the service personnel.
PA Series Biofeedback and Stimulation System User Manual Installation Chapter 3 Installation 3.1 Opening and Checking the Package The package is in large size and of heavy weight. Do not turn it upside-down. Visually examine the package prior to unpacking. If any signs of mishandling or damage are detected, contact the carrier to claim for damage. Open the package and check the components according to the packing list. Inspect the components for any damage.
PA Series Biofeedback and Stimulation System User Manual Basic Functions and Operations Chapter 4 Basic Functions and Operations 4.1 Connecting to Patient Connect one end of the sensor cable to the channel interface of the main unit, and connect the other end of the sensor cable to the interface of sensor/probe/electrodes. Reference electrode should be connected when collecting EMG signals. Operate per the sensor/probe/electrodes’ user manual. Adhesive electrodes placement is shown as below.
PA Series Biofeedback and Stimulation System User Manual Basic Functions and Operations counterclockwise to decrease the current intensity. Only during the electrical stimulation output can the current be adjusted. The current cannot be adjusted during resting period. 4.
PA Series Biofeedback and Stimulation System User Manual Software Operations Chapter 5 *Software Operation 5.1 Starting up the Software After the device is turned on, the software login interface pops up automatically. The drop-down user name menu lists all the latest user names. Select a user name, input the correct password and then click Login to open the main interface. If it’s the first time to use the software, please use sys as the user name to log in, the default password is sys.
PA Series Biofeedback and Stimulation System User Manual Software Operations Figure 5-2 5.3.2 Adding Patient You can register and input the information of a new patient by clicking the See figure 5-3. button. Figure 5-3 You should at least input the Name and Age. Click Yes to save the patient information; click Cancel to give up adding the new patient. The newly added patient information will be updated to the patient list automatically.
PA Series Biofeedback and Stimulation System User Manual Software Operations 5.3.3 Searching Patient You can search the patient in the patient list or through searching function if the patient information is in the database. Input the patient’s name or phone number or code to search the patient, then the related patient will be displayed in the list. Select the patient, and enter the corresponding function interface. 5.3.
PA Series Biofeedback and Stimulation System User Manual Software Operations Figure 5-4 Quick screening, EMG screening, EMG evaluation and pressure screening include free training and formal assessment. Sexual function assessment, lumbago assessment and cough reflex assessment do not include free training. NOTE: If code is not filled during adding patient, click any mode under assessment, you will be informed to fill in the code. 5.4.1 Free Training The interface of Free Training is as follows.
PA Series Biofeedback and Stimulation System User Manual Software Operations Figure 5-5 Free training mainly helps patient learn to contract target muscles and be familiar with the contraction actions and contraction rhythms. Free training not only displays the template of fast twitch muscle contraction and slow twitch muscle contraction, but also plays the corresponding voice prompt. When the patient is familiar with the contraction actions and rhythms, click to enter formal screening.
PA Series Biofeedback and Stimulation System User Manual Software Operations 5.4.3 EMG Screening The interface of EMG Screening is similar to Free Training. As shown in figure 5-7, it has 4 phases: pre-resting phase (25s resting), fast contraction phase (fast contraction for 5 times), continuous contraction phase (continuous contraction for 5 times) and post-resting phase (25s resting), totally lasting 3 minutes and 25 seconds. Figure 5-7 5.4.
PA Series Biofeedback and Stimulation System User Manual Software Operations Figure 5-9 5.4.6 Lumbago Assessment The lumbago assessment is conducted by evaluating the lower back muscles when patient is bending down, getting up and relaxing under guidance. During the lumbago process, the actions of bending down, getting up and relaxing repeat three times, as shown in figure 5-10, totally lasting 1 minute and 33 seconds. Figure 5-10 5.4.
PA Series Biofeedback and Stimulation System User Manual Software Operations Figure 5-11 5.4.8 Cough Reflex Assessment The Cough Reflex Assessment includes 2 phases. Before each phase, there are corresponding voice prompts, cough reflex assessment voice prompts and message box prompts: This test measures the reflex rate and contractile muscle strength of pelvic floor muscles under cough condition, including three times of mild cough and three times of vigorous cough.
PA Series Biofeedback and Stimulation System User Manual Software Operations Treatment includes "Defined Protocol" and "Custom Protocol". Select the required protocol and click , and the parameter interface will pop out. The parameters can be adjusted, such as treatment time: 1-60min（1min step，±10%）. For the range of the other parameters, please Parameters. refer to A1.3 Performance Specifications-Stimulation 5.5.
PA Series Biofeedback and Stimulation System User Manual Pressure and Max. Value. After filling in the information, click Intelligent Protocol. Software Operations to generate an Figure 5-14 5.5.1.2 Fixed Protocol Select "Fixed Protocol" on the patient protocol interface, select a protocol type and click to generate a treatment protocol.
PA Series Biofeedback and Stimulation System User Manual Software Operations Figure 5-15 5.5.1.3 MVC Detection MVC is short for Maximum Voluntary Contraction. If an intelligent protocol is selected, the MVC Detection interface will pop up by default. The parameter and template are adjusted according to the single MVC result of the patient, as shown in the following figure.
PA Series Biofeedback and Stimulation System User Manual Software Operations Figure 5-16 If Fixed Protocol is selected and the protocol includes Kegel or biostim feedback programs, the MVC Detection interface will pop up during each treatment by default. The template is adjusted according to the single MVC result of the patient, as shown in the following figure. 5.5.1.
PA Series Biofeedback and Stimulation System User Manual Figure 5-17 Electro-Stim Figure 5-18 ETS 37 Software Operations
PA Series Biofeedback and Stimulation System User Manual Figure 5-19 Biostim feedback Figure 5-20 Kegel 38 Software Operations
PA Series Biofeedback and Stimulation System User Manual Figure 5-21 Scene Training Figure 5-22 Breath Relaxation 39 Software Operations
PA Series Biofeedback and Stimulation System User Manual Figure 5-23 Game Figure 5-24 Dilation 40 Software Operations
PA Series Biofeedback and Stimulation System User Manual Software Operations 5.5.2 Custom Treatment Figure 5-25 Custom Treatment The Custom Treatment supports user to assemble and adjust customized protocols referring to patient’s condition. The user can select appropriate protocol segments below, modify the parameters and add them to the phase framework. Click the Start Treatment button to start the treatment.
PA Series Biofeedback and Stimulation System User Manual Software Operations all” or “End all” button. Or the user can pause or end each one channel by corresponding button in its framework. Click Please choose protocol. If the parameter of the selected protocol needs modification, click the protocol, and then configure the current intensity of each channel. If the current intensity is confirmed to be appropriate, click Start all to start the treatment.
PA Series Biofeedback and Stimulation System User Manual Figure 5-27 Single Person 5.7 Database Click Database on the main interface to enter the Database interface.
PA Series Biofeedback and Stimulation System User Manual Software Operations 5.7.1 Patient Information Long press a patient, click Edit, the selected patient information modification interface will pop up, and the patient information can be modified. Click Delete to delete the selected patient information and all patient records. 5.7.2 Patient Record Preview Waveform: refers to section 5.3.4 Examine Report: refers to section 5.3.4 Data Review: refers to section 5.3.
PA Series Biofeedback and Stimulation System User Manual 5） Click the Save button Software Operations . NOTE: The user in different type can pick different authorization. The system manager defaults to have all authorizations; the director cannot pick "Setup"; the doctor and nurse cannot pick "Setup" and "Delete Historical Data". 5.8.1.4 Modifying User 1） Click the Setup button on the main interface. 2） Click User Setup. 3） Click Modify User.
PA Series Biofeedback and Stimulation System User Manual Software Operations Waveform/Template Size: sets the width of all waveforms/ template width in MVC detection on the Assessment and Treatment interface. Pressure Unit: Set the pressure unit in pressure assessment and report, the pressure unit is cmH2O by default. 5.8.2.2 Channel Settings Pelvic Floor: sets the corresponding channel of pelvic floor muscles in the Assessment and Treatment interface.
PA Series Biofeedback and Stimulation System User Manual Software Operations footer. Content Patient Information Report Information Report Title Page Footer Option Instructions Name Selected by default Age Selected by default Gender Selected by default Examining Time Selected by default Position Unselected by default Gravidity Selected by default Parity Selected by default Tel.
PA Series Biofeedback and Stimulation System User Manual Software Operations There are following buttons under Post-Birth Plan Library: Add, Delete, Up, Down, and Check. The operation method is the same as PF Plan Library. Import Protocol: Insert the mobile storage device into the USB interface and click Import Protocol. Select the protocol file, and click Import File. Select the imported protocol, and click Import Protocol to import. 5.8.5 Database 5.8.5.
PA Series Biofeedback and Stimulation System User Manual Software Operations 5.8.6 Communication Settings 5.8.6.1 Wifi Settings 1) Open the top menu, locate the WiFi , and long press to enter. 2) Select the device to connect, enter the device password, and click connect. 5.8.6.2 BT Settings 1) Open the top menu, locate the BT , and long press to enter. 2) Select the device to connect, enter the device password, and click connect. 5.8.6.3 NFC Settings 1) Open the top menu, click the NFC .
PA Series Biofeedback and Stimulation System User Manual Maintenance Chapter 6 Maintenance and Cleaning 6.1 Maintenance 6.1.1 Inspection (1) Visual Inspection Prior to using the system every time, perform the following inspections: 1） Check the system and accessories to see if there is any visible evidence of damage that may affect the patient's or operator's safety. 2） Check all the outer cables, power socket and power cables for damage and connection. 3） Check if the system functions properly.
PA Series Biofeedback and Stimulation System User Manual Care and Cleaning 6.2 Care and Cleaning Use only the EDAN-approved substances and methods listed in this chapter to clean or disinfect your equipment. Warranty does not cover damage caused by using unapproved substances or methods. EDAN Instruments has validated the cleaning and disinfection instructions included in this User Manual.
PA Series Biofeedback and Stimulation System User Manual Care and Cleaning ⚫ Do not allow liquid to enter the case. ⚫ Never use abrasive material (such as steel wool or silver polish). ⚫ Inspect the system and reusable accessories after they are cleaned and disinfected. CAUTION If you spill liquid on the equipment, battery, or accessories, or they are accidentally immersed in liquid, contact your service personnel or EDAN service engineer.
PA Series Biofeedback and Stimulation System User Manual Care and Cleaning 4. Leave them to air dry. 6.2.4 Disinfecting Clean the main unit and reusable accessories before they are disinfected. The validated disinfectants for disinfecting the main unit and reusable accessories are listed below. Refer to the disinfecting agent manufacturer's instruction for use with reference to concentration, temperature and contact time.
PA Series Biofeedback and Stimulation System User Manual Care and Cleaning example, the contact time recommended by the manufacturer for soaking in Cidex Glutaraldehyde (2.4%) is at least 45 min. 6. Rinse the vagina sensor/stress probe/rectum sensor thoroughly with sterile water to remove all chemical residues. For example, it is required to flush the sensor after soaking in Cidex Glutaraldehyde (2.4%) with plenty of sterile water (about 2 gallons) at least one time.
PA Series Biofeedback and Stimulation System User Manual Care and Cleaning Assembling and fitting patient-specific accessories and consumables. 6.2.6 Storage and Transport After reprocessing, there are no special requirements for storage and transport of the product. However, the following must be observed: – Store dry and free of dust – Avoid recontamination and damage during transport All further information on storage and transport included in the accompanying documents must be observed.
PA Series Biofeedback and Stimulation System User Manual Warranty and Service Chapter 7 Warranty and Service 7.1 Warranty EDAN warrants that EDAN's products meet the labeled specifications of the products and will be free from defects in materials and workmanship that occur within warranty period. The warranty is void in cases of: a) damage caused by mishandling during shipping. b) subsequent damage caused by improper use or maintenance.
PA Series Biofeedback and Stimulation System User Manual Product Specification Appendix 1Product Specifications NOTE: Specifications of the system are shown in its accompany file. A1.1 Environmental Specifications Temperature: 0 ºC ~ + 40 ºC Working Relative Humidity: 15%RH ~ 95%RH（non-condensing） Atmospheric Pressure: 86kPa ~ 106kPa Temperature: -20 ºC ~ +55 ºC Transport Storage and Relative Humidity: 15%RH ~ 95%RH（non-condensing） Atmospheric Pressure: 70kPa ~ 106kPa A1.
PA Series Biofeedback and Stimulation System User Manual Water Product Specification proof) Degree of Safety in Equipment not suitable for use in presence of flammable Presence of Flammable gases Gases Disinfection/Sterilizing Method Refer to this user manual for details EMC CISPR 11Group 1 Class B A1.3 Performance Specifications EMG Parameters Measurement Range 1uV ~3000uV Accuracy 1µV ~20µV（±2μV）or 21µV ~3000µV（±10%） Definition ≦0.
PA Series Biofeedback and Stimulation System User Manual Product Specification A1.4 Rechargeable Lithium-ion Battery Type Rechargeable Lithium-ion Battery Continual Working Time ≥8 hours Necessary charge time from "out of power" to ≤7 hours (stand by or power off status) "fully charged" Necessary charge time from "out of power" to ≤6.5 hours (stand by or power off status) "90% charged" Nominal Capacity ≥6000mAH Nominal Voltage 14.
PA Series Biofeedback and Stimulation System User Manual Troubleshooting Appendix 2 Troubleshooting A2.1 Trouble with Starting Up Phenomenon Possible Cause Solution The power supply is faulty. Replace the power supply. Power input is in poor contact. Check the power input. Abrupt switching off. The main control board is Replace faulty. board. the main control The boot interface board is Replace the boot interface faulty. board. A2.
PA Series Biofeedback and Stimulation System User Manual Troubleshooting The device or power Ground the device or the power supply is not grounded. supply. The patient is nervous or the position is wrong, Guide the patient to relax and adjust and the actual EMG the position. signal is higher. The electrodes are not provided by EDAN. The contact of the electrode Use electrodes provided by EADN or connector is so poor that electrodes that are suitable. leads to the change of skin impedance.
PA Series Biofeedback and Stimulation System User Manual Troubleshooting skin impedance. The reference electrode Check whether the reference electrode is not well connected.
PA Series Biofeedback and Stimulation System User Manual EMC Information Appendix3 EMC Information A3.1 Electromagnetic Emissions Guidance and manufacture’s declaration – electromagnetic emission The PA Biofeedback and Stimulation System is intended for use in the electromagnetic environment specified below. The customer or the user of the Biofeedback and Stimulation System should assure that it is used in such an environment.
PA Series Biofeedback and Stimulation System User Manual EMC Information A3.2 Electromagnetic Immunity Guidance and manufacture’s declaration – electromagnetic immunity The PA Biofeedback and Stimulation system is intended for use in the electromagnetic environment specified below. The customer or the user of the PA Biofeedback and Stimulation System should assure that it is used in such an environment.
PA Series Biofeedback and Stimulation System User Manual 0 % UT; 0,5 cycle At 0°, 45°, 90°, 135°, 180°, 225°, 270°and 315° Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11 0 % UT; 1 cycle and 70 % UT; 25/30 cycles ) Single phase: at 0° 0 % UT; 250/300 cycle EMC Information 0 % UT; 0,5 cycle At 0°, 45°, 90°, 135°, 180°, 225°, 270°and Mains power quality should be 315° that of a typical commercial or hospital environment.
PA Series Biofeedback and Stimulation System User Manual d = 1.2 P 150 kHz to 80 MHz Conducted RF 3 Vrms 3 Vrms IEC 61000-4-6 150 kHz to 80 MHz 150 kHz to 80 MHz 6Vrmsc)in ISM bands between 0,15 MHz and 80 MHz EMC Information 6Vrmsc)in ISM bands between 0,15 MHz and 80 MHz Radiated RF 3 V/m 3 V/m d = 1.2 P 80 MHz to 800 MHz IEC 61000-4-3 80 MHz to 2.7 GHz 80 MHz to 2.7 GHz d = 2.3 P 800 MHz to 2.
PA Series Biofeedback and Stimulation System User Manual EMC Information a) Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered.
PA Series Biofeedback and Stimulation System User Manual WLAN,802.11 b/g/n, RFID 2450, LTE Brand 7 5240 5500 5100-5800 WLAN a/n 802.11 5785 EMC Information modulationb) 217 Hz Pulse modulationb) 217 Hz 0.2 0.3 9 Note: If necessary to achieve the IMMUNITY TEST LEVEL, the distance between the transmitting antenna and the ME EQUIPMENT or ME SYSTEM maybe reduce to 1m. The 1 m test distance is permitted by IEC 61000-4-3. a) For some services, only the uplink frequencies are included.
PA Series Biofeedback and Stimulation System User Manual EMC Information For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
PA Series Biofeedback and Stimulation System User Manual Ordering Information Appendix 4 Ordering Information CAUTION Only the parts supplied by the manufacturer should be used with the system. Part Number Accessories 01.57.472216 Sensor Cable（1.6 m，with 3 branches） 01.57.472178 Sensor Cable（1.8 m，with 3 branches） 01.57.472215 Sensor Cable（1.8 m，with 5 branches） 02.57.225123 Vagina Sensor SV1 02.57.225124 Vagina Sensor SV2 01.57.472020 EMG/Stimulation sensor 01.57.
