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Statement
Beijing Aeonmed Co, Ltd. (Aeonmed for short) holds the copyrights to this manual, which is
non-public published, and reserves the rights to keep it as a secure document. Refer to this
manual when operating, maintaining and repairing Aeonmed products only. Anyone other than
Aeonmed may not make it known to others.
Proprietary materials protected by the copyright law are included in this manual. Any section of
it cannot be reproduced, copied, or translated into other languages without any prior written
approval from Aeonmed who reserves the copyright.
Everything written in this manual is considered to be correct. Aeonmed is not legally
responsible for any mistakes printed within and any damages caused by incorrect connection
and operation. Aeonmed does not supply privileges endowed by the patent law to any other
parties. Aeonmed is not legally responsible for the results caused by patent law breaking and
any rights of the third party violating.
Refer to this manual before any Aeonmed product is used. The manual includes operating
procedures which must be performed with cautiously, operations that may result in non-normal
working conditions and the dangers which may damage equipment or cause bodily harm.
Aeonmed is not responsible for the security, reliability and function of the equipment in case
that the dangers, damages and non-normal phenomenon mentioned in this manual happen.
Free repairs for these malfunctions will not be provided by Aeonmed.
Aeonmed have the rights to replace any content in this manual without notice.
Manufacturer Responsibility
Aeonmed is responsible for the security, reliability and function of the equipment when to
following conditions are adhered to:
Connection, adjustments, mending and repairs must be performed by individuals
authorized by Aeonmed;
Necessary electrical equipment and the working environment must be in accordance with
the national standards, professional standards and the requirements listed in this manual;
Equipment must be used as instructed in the operating instructions.
The paid theoretical framework diagram will be supplied according to customer requirements
by Aeonmed, plus calibrating method and other information to help the customer, under the
assistance of qualified technicians, repair the equipment parts where can be done by customer
himself based on the stipulation by Aeonmed.
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Troubleshooting
Related Manuals for Aeonmed Shangrila510s
Summary of Contents for Aeonmed Shangrila510s
- Page 1 Statement Beijing Aeonmed Co, Ltd. (Aeonmed for short) holds the copyrights to this manual, which is non-public published, and reserves the rights to keep it as a secure document. Refer to this manual when operating, maintaining and repairing Aeonmed products only. Anyone other than Aeonmed may not make it known to others.
- Page 2 Aeonmed’s obligation under the above warranties does not include the freight and other fees. Aeonmed is not responsible for any direct, indirect or final product broken and delay which result from improper use, alteration by using the assemblies ungratified and maintenance by anyone other than Aeonmed.
- Page 3 Follow the steps in case that the product needs to be returned to Aeonmed: 1. Obtain the rights of return Contact with the customer service of Aeonmed by informing them the number and type of the product. The number is marked on the surface of the product. Return is unacceptable if the number cannot be identified.
- Page 4 Warning for use Thank you for purchasing an AEONMED Shangrila510s Ventilator. In order to use this product correctly and effectively, please read these operating instructions carefully and completely before using the product for the first time. When using the product, always proceed in accordance with the information provided in these operating instructions as detailed in this user manual.
- Page 5 Manufacturer(holder): Beijing Aeonmed Co., Ltd. Manufacturer(holder) Room 405，Basement 1 to 4th Floor of 901 Unit, address: Building 9, No.26 Outer Ring West Road, Fengtai District, Beijing 100070, China Facility: Beijing Aeonmed Co., Ltd. Room 405，Basement 1 to 4th Floor of 901 Unit, Facility address: Building 9, No.26 Outer Ring West Road, Fengtai...
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Page 6: Table Of Contents
Contents Introduction ........................1-1 Product Description for Shangrila510S ..............1-1 1.1.1 Intended Use ..................... 1-1 1.1.2 Contraindication ..................1-2 Symbols ........................ 1-2 Warnings and Cautions ..................1-3 1.3.1 Warnings....................1-3 1.3.2 Cautions ....................1-5 Frequently Used Functions .................. 1-6 Definitions, Acronyms, and Abbreviations ............1-7 Structure .......................... - Page 7 Power on ......................5-5 Clean, disinfect and sterilize ................... 6-1 User Maintenance ......................7-1 Repair Policy ......................7-1 Maintaining Outline and Schedule ............... 7-2 7.2.1 User Maintenance ..................7-2 7.2.2 Useful Life Estimation................7-2 Replacing Fuses....................7-3 Maintaining Battery....................7-3 Alarm and Troubleshooting .....................
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Page 9: Introduction
WARNING: Shangrila510S is unsuitable for use in a magnetic resonance imaging (MRI) environment. 1.1.1 Intended Use Shangrila510S is intended to be used for adult, child and infant patients weighting over 3.5kg for ventilation assistance and respiratory support in general ward, recovery room and emergency department. -
Page 10: Contraindication
1.1.2 Contraindication The Shangrila510S ventilator has no contraindications to its use at present. 1.2 Symbols Instead of illustrations, other symbols may also be utilized. Not all of them may necessarily appear in the equipment and manual. The symbols include: Power supply switch... -
Page 11: Warnings And Cautions
1 Introduction Manual 1.3 Warnings and Cautions WARNING and CAUTION indicate all the possible dangers in case of violation of the stipulations in this manual. Refer to and follow them. WARNING: indicates potential hazards to operators or patients CAUTION: indicates potential damage to equipment 1.3.1 Warnings WARNING: Do not use the system until you have read and understood this manual including:... - Page 12 WARNING: 510S ventilator is not intended to be a comprehensive monitoring device and does not activate alarms for all types of dangerous conditions for patients on life-support equipment. WARNING: Patients on life-support equipment must be appropriately monitored by competent medical personnel and suitable monitoring devices at all times. WARNING: Patients on ventilator should be appropriately monitored by competent medical personnel and suitable monitoring devices.
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Page 13: Cautions
Aeonmed recognizes that cleaning, sterilization, sanitation, and disinfection practices vary widely among health care institutions. It is not possible for Aeonmed to specify or require specific practices that will meet all needs, or to be responsible for the effectiveness of cleaning, sterilization, and other practices carried out in the patient care setting. -
Page 14: Frequently Used Functions
CAUTION: To avoid a fire hazard, keep matches, lighted cigarettes, and all other sources of ignition (e.g., flammable anesthetics and/or heaters) away from 510S ventilator and oxygen hoses. CAUTION: In case of fire or a burning odor, immediately disconnect the ventilator from the oxygen supply, facility power and backup power source. -
Page 15: Definitions, Acronyms, And Abbreviations
1 Introduction (10) System interconnections for gas supply 1.5 Definitions, Acronyms, and Abbreviations CPAP Continuous Positive Airway Pressure (setting) Respiratory rate, i.e. breaths per minute (setting) Total respiratory rate, i.e. sum of and f (monitored) total spont Delivered oxygen percentage (setting and monitored data) I : E Inspiration to expiration time, I to E ratio, (monitored) Exhaled minute volume (monitored) -
Page 17: Structure
2 Structure 2 Structure CAUTION: The conditions of parameters monitoring in this system are as follows: the environment temperature: 23 ℃; gas temperature 25 ℃; humidity: 50%; Gas: oxygen. WARNING: Do not use antistatic or electrically-conductive breathing tubes and mask. 2.1 510S Profile Figure 2-1 Main unit... -
Page 18: Front Panel
2.2 Front Panel The front panel is composed of display area, function keys, free to define keys, knob, indicator light and power switch. Figure 2-2 Display area The windows of follow figure is display area, it contains: Patient Type, Patient Measured Parameters, Alarm Messages, AC and Battery indicators, Waveforms etc. - Page 19 2 Structure Function keys Figure 2-4 In Figure 2-4, the part of the rectangle is function keys, include: six ventilation modes，that is 【A/C-V】 ， 【SIMV-V】 ， 【 SPONT/PSV 】 ， 【 A/C-P 】 （ optional ） ， 【 CPAP 】 mode：...
- Page 20 Free to define keys Figure 2-5 CAUTION: If the [Psens] key is depressed the mode will change to [Vsens]. Knobs Figure 2-6 knob： Adjusts the value of a setting.
- Page 21 2 Structure ： Adjust the oxygen concentration of the machine Peak Flow Adjust the flow rate to control the tidal volume of the setting： machine CAUTION: Do not overexert when you adjust the knobs. Indicator light and power switch Figure 2-7 Press power switch, the machine will enter starting up Power switch: test.
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Page 22: Right Side Panel
2.3 Right Side Panel Figure 2-8 Flow sampling port Control port Inspiratory port （optional） Power socket Fuse RS232 interface sensor port Control port: It can control the open and close of the expiration valve. Flow sampling port: is located at the closest position to the patient inspiration end, so it can provide accurate monitoring of VT and MV. -
Page 23: Left Side Panel
2 Structure sensor port: Installing O sensor, O sensor is used to measure O concentration. CAUTION: The equipment which connects the ventilator by RS232 port, must comply with IEC60601-1. 2.4 Left Side Panel In the left-hand side panel of the ventilator, there is a window which can open. This is the internal battery replace window. -
Page 24: Back Side Panel
2.5 Back Side Panel Figure 2-10 Emergency air intake：Do not obstruct. Exhaust port：Do not obstruct. Safety valve Buzzer... -
Page 25: Operating Guide
3 Operating Guide 3 Operating Guide WARNING: Do not connect to the patient before finish the patient setting. This ventilator was designed for patient safety and security, but always monitor the patient’s clinical state in conjunction with the ventilator display and settings. CAUTION: ... -
Page 26: Setup Ventilation Mode
If starting-up is passed, display shows the patient type [adult], [children], [infant]. According to the situation of the patient choose patient type. See right figure 3.2 Setup Ventilation Mode Step 1： Press the key, enter [mode] interface, as shown in the right figure. -
Page 27: Ventilation Mode Introduction
3 Operating Guide 3.3 Ventilation Mode Introduction 3.3.1 A/C In A/C mode, the ventilator delivers only mandatory breaths. When the ventilator detects patient inspiratory effort, it delivers a patient-initiated mandatory (PIM) breathe (also called an assisted breath). If the ventilator does not detect inspiratory effort, it delivers a ventilator-initiated mandatory (VIM) breath (also called a control breath) at an interval based on the set respiratory rate. -
Page 28: A/C-V
3.3.2 A/C-V A/C-V (Volume Control Ventilation) is mandatory ventilation with preset respiratory frequency and tidal volume. When ventilator detects patient’s spontaneous breath, it will work according to the above settings. Tidal volume adjustment: according to the frequency and I:E set by the ventilator , observe the VT monitoring value on the screen, and adjust the VT to the expected value by adjusting the peak flow. -
Page 29: Cpap
3 Operating Guide assisted breath) or a ventilator-initiated mandatory (VIM) breath (in case the patient’s inspiratory effort is not sensed within the breath cycle). As shown in Figure 3-4, each SIMV breath cycle (Tb) has two parts: the first part of the cycle is the mandatory interval (Tm) and is reserved for a PIM. - Page 30 Figure 3-5 Press the free to define key of【f】 ， 【f】turns yellow，as shown in the below figure. Figure 3-6 Rotate the knob to adjust value until the wanted, and then press it again to confirm.
- Page 31 3 Operating Guide Figure 3-7 Figure 3-8 Setting procedure about other parameters is similar to one above. When ventilation mode is changed, the values of the parameter keys displayed will change to correspond to the new ventilation mode. CAUTION: If the knob is not pressed for confirmation, the previous value will be displayed. The following conditions should be noticed in parameter setting: a) Pressure parameter setting is subject to high pressure limit.
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Page 32: Alarm Settings
3.5 Alarm Settings There are the following parameters can be set: Alarm parameter Meaning unit Minute volume upper limit and lower limit Airway pressure upper limit and lower limit 0.1kPa Oxygen concentration upper limit and lower limit —— Setting method as shown in the following: ”... - Page 33 3 Operating Guide Figure 3-10 Figure 3-11 Turn the knob to select appropriate value and depress the knob..
- Page 34 Figure 3-12 CAUTION: If “Accept” is not clicked, the screen will return to the main menu after 10 seconds, and the last setup changes made will have no effect. CAUTION: In the case of an alarm during operation, the following scenarios may have occurred: Improper breathing parameter setting or alarm limit setting;...
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Page 35: System
3 Operating Guide 3.6 System ” on the front panel, Turn the knob, move to 【System】 key, press Press the menu key “ knob, enter into 【System】 interface. Figure 3-13 Figure 3-14 3-11... -
Page 36: Unit
3.6.1 Unit Turn the knob, move to 【Unit】 key, press knob, enter into 【Unit】 interface. Figure 3-15 Unit: cmH O、0.1kPa、mBar. When pressure unit changed, the Y-axis unit of waveforms changed in-phase and keep identical. 3.6.2 Language Turn the knob, move to 【Language】 key, press knob, enter into 【Language】 interface. Figure 3-16 3-12... -
Page 37: Waveform
3 Operating Guide Language：Chinese, English, Spanish, and so on. 3.6.3 Waveform Turn the knob, move to 【Waveform】 key and press knob, enter into 【Waveform】 interface. Figure 3-17 Waveform style: Paw-t and Flow-t. 3.6.4 Trace Select Turn the knob, move to 【Trace select】 key and press knob, enter into 【Trace select】 interface. -
Page 38: Calibration
Waveforms two types: Block and Line. 3.6.5 Calibration Turn the knob, move to 【Calibration】 key and press knob, enter into 【Calibration】 interface. Figure 3-19 The calibration choices include: Pressure Sensor Calibration, O Sensor Calibration, elevation compensation, Flow Sensor Calibration, Expiratory Valve Calibration. 3.6.5.1 Pressure Sensor Calibration Press “Pressure Sensor”... - Page 39 3 Operating Guide Press “Start” to start pressure sensor calibration. A progress bar will be displayed. After calibration, the result will appear: Calibration succeeded or Calibration failed. If failed, restart the calibration. NOTE: During this period no, other operation can be performed. Clicking other areas will have no response.
- Page 40 Figure 3-22 "21%" calibration: remove the oxygen battery from the gas circuit of the ventilator, put it in the air for at least 3 minutes, press the “shuttle button” to confirm, and the ventilator will perform the calibration. "100%" calibration: 1.
- Page 41 3 Operating Guide NOTE: Please disconnect the wiring plug when disassembling the oxygen concentration sensor and be careful not to damage the wiring. 3.6.5.3 Flow Sensor Press “Flow Sensor” to enter the interface. A message is displayed: “To offset zero of flow sensor, please remove the circuit from the ventilator.”...
- Page 42 Figure 3-25 Connect the breathing circuit, connect the gas resistance connector of the ventilator self-contained to the test lung, and adjust the flow rate knob to about 3/4 of the full range. Press the “Start” button to start Expiratory Valve Calibration, the remaining procedure is the same as the pressure sensor calibration.
- Page 43 3 Operating Guide A message box appears. Input desired new altitude in the message box then press knob to confirm it. Figure 3-27 Figure 3-28 NOTE: The altitude measurement is meters. 3-19...
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Page 44: Patient Data Menu
3.7 Patient Data Menu This area displays all of the monitored patient parameters including VT, MV, PEEP, Ppeak, Ftotal, FiO Figure 3-29 3.8 Turn off the Ventilator (1) Disconnect the breathing hoses from the patient. (2) Turn off the power switch. (3) Disconnect the gas supply. -
Page 45: Pre-Use Test
4 Pre-use Test 4 Pre-use Test 4.1 AC Failure Alarm Test Turn on power switch “ ” on the front panel, the ventilator is started,enters into A/C ventilation mode interface after self-test. After the ventilator operates for five minutes, pull out power cord. Make sure that power failure alarm occurs( alarm bell sounds;... -
Page 46: Breathing System Test
Low Oxygen Concentration Alarm FunctionTest The ventilator works in the standard state, Ventilation for more than 2 minutes,after the oxygen concentration monitoring is stable, adjust the oxygen concentration lower limit value in the alarm setting area,the oxygen concentration lower limit value is slightly higher than the monitoring value of the ventilator, and there should be a sound and light alarm. - Page 47 4 Pre-use Test SIGH Let the ventilator work at a standard work state, record the tidal volume. Then change ventilation mode to SIGH, adjust the airway upper limit pressure to maximum, see the display of the tidal volume data, it should 1.5 time as normal the second time respiration takes place. This happens every 100 times, during this ventilation mode.
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Page 49: Connection
5 Connection WARNING: To prevent generating wrong data and malfunction, please use the cables, hoses, and tubes from Aeonmed. WARNING: The operator will have to ensure that the inspiratory and expiratory resistances are not exceeded when adding attachments or other components or sub-assemblies to the breathing system. -
Page 50: Connect Oxygen Supply And Patient Circuit
5.2 Connect Oxygen Supply and Patient Circuit Shangrila510S can work with oxygen bottle gas supply in the ambulance or on the wall. When the ventilator is working, make sure the gas supply has been connected without any false, no break, no leak or wrong connecting, and check the pressure monitor is right. - Page 51 5 Connection Step 2 Connect pressure controlling pipe Step 3 Connect the O inlet pipe Step 4 Connect flow sampling pipe Step 5 Connect gas outlet pipe to breath valve Step 6 Connect pressure controlling pipe Step 7 Connect flow sampling probe...
- Page 52 ISO-standard cone and socket. Aeonmed recommends that you use one of the patient circuits identified by Aeonmed, or their equivalents to ensure that the maximum pressure/flow values specified by EN794-1 are not exceeded (see related content in part 9 specifications). Using a circuit with a higher resistance does not prevent ventilation but can cause compromise the patient’s ability to...
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Page 53: Power On
5 Connection 5.3 Power on Press the power button, all indicator lights on the front panel are ON together with a short buzz. If something abnormal happened, stop using the ventilator immediately, and connect the manufacturer for some repairing. Details about it will be displayed in the section 8 Alarm and Troubleshooting. -
Page 55: Clean, Disinfect And Sterilize
6 Clean, disinfect and sterilize 6 Clean, disinfect and sterilize WARNING: Use a cleaning, disinfection and sterilizing schedule that conforms to your institution’s sterilization and risk-management policies. Refer to the material safety data policy of each agent. Refer to the operating and maintaining manual of all the sterilizing equipment’s. ... - Page 56 Steam disinfection is a viable disinfecting method of Shangrila510S patient circuits supplied by Aeonmed, but it may shorten the tubing’s life span. Discoloration (yellowing) and decreased tubing flexibility are expected side effects of steam disinfecting this tubing. These effects are cumulative and irreversible.
- Page 57 6 Clean, disinfect and sterilize Vacuum Pressure: 20psig(138kPa) Drying Time: 20minutes CAUTION: Disposable breathing hoses must not be reused. Reuse of the single use hoses can cause cross infection and patient harm.
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Page 59: User Maintenance
It is recommended that you replace damaged parts with components manufactured or sold by Aeonmed. After any repair work, test the unit to ensure it complies with the manufacturer’s published specifications. Contact the nearest Aeonmed Service Center for service assistance. In all cases, other than where Aeonmed’s warranty is applicable, repairs will be made at Aeonmed’s current list price... -
Page 60: Maintaining Outline And Schedule
7.2 Maintaining Outline and Schedule The schedule is designed based on the typical condition, that is to say, the least maintenance times is 2000h operating per year. In case the actual operating time is longer than 2000h per year, the maintenance times should be more. 7.2.1 User Maintenance Minimum maintenance interval Task... -
Page 61: Replacing Fuses
7 User Maintenance 7.3 Replacing Fuses WARNING: Disconnect from power supply before replacing fuses. This may injure or cause death of the operator. Replace fuses with only those of the specified type and current rating, otherwise this can damage the equipment. - Page 62 Same model battery with CE certification is suggested. CAUTION: An authorized Aeonmed services representative can replace battery. If the battery is not used for a long-time, please contact Aeonmed service representatives to disconnect the battery. The waste battery should be disposed in accordance with the local regulations.
- Page 63 7 User Maintenance International, Inc for reprocessing. The separate collection and recycling of your waste equipment at the time of disposal will help to conserve natural resources and ensure that it is recycled in a manner that protects human health and the environment. For more information about where you can drop off your waste equipment for recycling, please contact your local city office, your waste disposal service, or your product distributor or retailer.
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Page 65: Alarm And Troubleshooting
8 Alarm and Troubleshooting 8 Alarm and Troubleshooting WARNING: No repair should ever be undertaken or attempted by anyone without proper qualifications and equipment. 8.1 About Alarm The operator may be positioned anywhere around the unit to view the alarm light. The alarm light is visible from a distance of 3 meters. -
Page 66: Alarm Message List
Figure 8-1 Alarm message area Ventilation mode Alarm mute time Alarm messages Patient type Alarm level Power supply and battery indicator NOTE: If a high-priority alarm goes away spontaneously (autoresets), its message remains lit with blue background (not flashing) until you press the alarm reset key. NOTE: When alarm silencing, the alarm bell has dashed “X”... - Page 67 8 Alarm and Troubleshooting Message Priority Type Alarm definition Operator action Check patient MV High!! Medium Physiological MV greater than high limit. and settings. Charge battery quickly. Under the battery operation, Battery High Technical the remaining battery run Obtain alternative Low!!! time is less than 10min.
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Page 68: Troubleshooting
8.3 Troubleshooting Symptom Possible Cause Recommended Action Power supply cable Plug in power supply cable unplugged Ventilator does not work Turn on power switch Power switch is off Replace with a new fuse Fuse is burned Ventilator stops operating manual ventilation, suddenly, indicator light Power supply is interrupted... -
Page 69: Specifications
Electromagnetic Compatibility (EMC): According to IEC 60601-1-2:2014 9.2 Physical Specification All specifications are approximately, maybe changed at any moment without notice. CAUTION: Do not put Shangrila510S into the shock environment. CAUTION: Do not lay the heavy on the top. Size 300mm(H)×168mm(W)×156mm(D) -
Page 70: Environment Requirements
9.3 Environment Requirements Operation: -18℃～+50℃ Temperature Storage: -20℃-60℃ Transport: -40℃～+70℃ Operation: 15%～95%, non-condensing Relative humidity Storage: 10%～95 % Transport: 10%～100% Operation: 70～110kPa Atmospheric Pressure Storage: 50～110kPa Transport: 50～110kPa CAUTION: The device should be stored in a room with good ventilation in which there are no corrosive gas. -
Page 71: Gas Supply
9 Specifications 9.4.2 Gas Supply Gas supply Composition: Compress O Pressure: 0.25MPa～0.6MPa Flow Max 180L/min CAUTION: All gas must be medical grade. CAUTION: If gas supply pressure less than 0.25MPa, there will be Gas supply down alarm, Thia may affect tidal volume. 9.4.3 Power Supply Voltage AC100V～240V, 50Hz/60Hz or DC12V;... -
Page 72: Operation Principle
9.6 Operation Principle... -
Page 73: Performance Parameters
Meet requirements for Class II, type B equipment specified in Electrical safety EN60601-1 Medical Electrical equipment: Part one: General requirement for safety. According to EN 60601-1, Shangrila510S belongs to the following classifications: Classification Class II, Type B, General, portable equipment. -
Page 74: Setting Ventilating Parameters
9.7.3 Setting Ventilating Parameters Based on the principle of ventilator, the value of oxygen concentration can be satisfied under standard conditions, but the accuracy of oxygen concentration will deviate under some boundary conditions. Item Range Resolution Accuracy Remark ±40mL（≤200mL） ； 0～2000mL ---- Peak flow = V... -
Page 75: The Effect Of Tidal Volume And Fio
9 Specifications Item Range Accuracy - upper limit ±10% OFF，50%～100%, default OFF - lower limit OFF，35%～99%, default 40% ±10% -upper limit 6 cmH O～80 cmH O, default 40 cmH ±2cmH O or ±10% -lower limit 0 cmH O～40 cmH O, default 5 cmH ±2cmH O or ±10% CAUTION:... -
Page 76: Emc Guidelines
Important information regarding Electro Magnetic Compatibility (EMC): Shangrila510S VENTILATOR needs special precautions regarding EMC and put into service according to the EMC information provided in the user manual; Shangrila510S conforms to this IEC 60601-1-2:2014 standard for both immunity and emissions. Nevertheless, special precautions need to be observed. - Page 77 9 Specifications EMI Compliance Table Table 1 - Emission Phenomenon Compliance Electromagnetic environment RF emissions CISPR 11 Professional healthcare facility environment Group 1, Class A Harmonic distortion IEC 61000-3-2 Professional healthcare facility environment Class A Voltage fluctuations IEC 61000-3-3 Professional healthcare facility environment and flicker Compliance EMS Compliance Table...
- Page 78 Table 4 – Input a.c. power Port Phenomenon Basic Immunity test levels standard Professional healthcare facility environment Electrical fast IEC 61000-4-4 ±2 kV transients/burst 100kHz repetition frequency Surges IEC 61000-4-5 ±0.5 kV, ±1 kV Line-to-line Surges IEC 61000-4-5 ±0.5 kV, ±1 kV, ±2 kV Line-to-ground Conducted IEC 61000-4-6...
- Page 79 This manual No.: 130015824 CE mark in this manual applies only to product with CE mark. Directive 93/42/EEC concerning Medical Devices Beijing Aeonmed Co., Ltd. Tel: +86-10-83681616 Fax: +86-10-83681616-8130 E-Mail: service@aeonmed.com Website: http://www.aeonmed.com Edition: V00.10 June 2021...
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