Infusion Monitor User Manual Zhejiang Zhier Information Technology Co., Ltd. Version, Manual Vision 1.
Table of Contents 1. Application and contraindications .......................................... 1 2. Product Composition .............................................................. 1 3. Product Performance and Basic Parameters .......................... 2 4. Product Model and specifications .......................................... 2 5. Product Working Principle ...................................................... 3 6. Installation ....................................................................
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1. Application and contraindications Application, This product is used to monitor the infusion status of patients during infusion, which is convenient for emergency treatment in abnormal situations. Contraindications, Can not be used for infusion monitoring of insulin, analgesics, chemotherapy drugs, etc. 2. Product Composition The infusion monitor is mainly composed of the circuit board, battery, sensor, LCD screen, motor, shell and software (version V1.1.0).
technology to sense the droplet passing in the infusion tube per unit time in real time to obtain the liquid dripping speed during the infusion process. When the infusion is completed and the empty bottle status is displayed, the infusion monitor will automatically block the infusion tube , To effectively prevent the patient's blood from flowing back. 3. Product Performance and Basic Parameters Product main performance index, 1. Infusion monitoring range, 10 drops / min‐100 drops / min. 2.
changes to the overall architecture. The second field identifies the minor version number of the software, relative to the major version, the minor version number upgrade corresponds to a partial change. However, this local change caused the program to be incompatible with the previous version, or caused damage to the previous collaborative relationship of the program, or a major improvement or enhancement in functionality.
infusion tube. When the tube is empty, it is a capacitance value. The capacitance value will change when there is a liquid medicine. . Infusion interception function: When the infusion completion status is detected, the motor is controlled by the MCU to rotate the gear to block the upper end of the infusion tube to achieve the interception function. 6. Installation Use the hook to hook the hanging hole of the infusion monitor, and then hang it on the hook of the infusion rod.
monitor. The infusion monitor will automatically detect the drip rate. 4.When the battery level on the device is low, you need to connect the charger to charge. During charging, LED1 (yellow) will blink continuously until the LED1 light is always on which means charge completed. LED2 is the work indicator light. 5.
5. Hang the barb of the infusion tube upside down in the hook hole of the infusion 2. Turn off the left infusion cover, adjust the infusion rate. The left infusion controller will monitor the monitor drop rate and send to the right side display through 4. Press the power button infrared, infusion start. to The display status‐‐ it will start the infusion monitor. display the drop rate when The display will show the status 1. When the left drop 3.
9. Maintenance 1. The infusion monitor is powered by a rechargeable lithium battery. Try not to overcharge and over discharge. When the battery power shows a space, it needs to be charged in time. The charging voltage is DC5V and the current is less than 1A. When the charging indicator (LED1) light is on You can stop charging. 2. After using the infusion monitor once, the nurse or a special person can check the displayed power to see if it shows that the low power needs to be charged. 3.
12. Explanation of graphic symbols Number of drops Infusion Liquid deficit Battery Complete infusion Lock down after infusion finished 13. Basic Troubleshooting Table1, Troubleshooting list SN Problem 1 Solution Check if the infrared tube is blocked or if there is liquid medicine at the liquid sensing position. First block the light to see if it is restored. If it is restored, it is light interference and needs to be returned to the factory for inspection.
14. Packing List Table2, Packing list SN Name Quantity Unit 1 Infusion Monitor 1 Set. 2 Hanging rod 1 Pcs. 3 Instructions 1 Pcs. 4 Packing list 1 Pcs. 15. Electromagnetic compatibility instructions This product (infusion monitor) requires special precautions regarding electromagnetic compatibility (EMC) and must be installed and used in accordance with the relevant information provided in this user manual.
Guidance and manufacturer's statement‐electromagnetic emissions This product (E‐SY01) is expected to be used in the electromagnetic environment specified below, and the purchaser or user should ensure that it is used in this electromagnetic environment: Emission Test Compliance Electromagnetic environment‐ Guidelines Radio frequency emission GB4824 Group 1 This product (E‐SY01) uses radio frequency energy only for its internal functions.
Guidance and manufacturer's declaration‐Electromagnetic immunity This product (E‐SY01) is expected to be used in the electromagnetic environment specified below, the purchaser or user should ensure that it is used in this electromagnetic environment: Immunity Test IEC60601 Test Level Conforming level Electrostatic discharge GB/T 17626.2 ± 6kV Contact discharge ± 8kV Air discharge ± 6kV Contact discharge ± 8kV Air discharge Electrical fast transient burst GB/T 17626.4 ± 2kV to power line.
Power frequency magnetic field 3A/m （50 Hz） GB/T 17626.8 3A/m The power frequency magnetic field should have the level characteristic of power frequency magnetic field in a typical place in a typical commercial or hospital Environment. Note: UT refers to the AC grid voltage before the test voltage is applied.
Guidance and manufacturer's declaration‐electromagnetic immunity This product (E‐SY01) is expected to be used in the electromagnetic environment specified below. The purchaser or user should ensure that it is used in this electromagnetic environment: Immunity Test Conducted RF GB/T17626.6 Radiated RF GB/T17626.3 IEC60601 Test Level 3 Vrms 150 kHz to 80 MHz 3 V/m 80 MHz to 2.
Guidance and manufacturer's declaration‐electromagnetic immunity This product (E‐SY01) is expected to be used in the electromagnetic environment specified below. The purchaser or user should ensure that it is used in this electromagnetic environment: Immunity Test IEC60601 Test Level Conforming Level Electromagnetic environment‐guide A.
Recommended separation distance between portable and mobile RF communication equipment with this product (E‐SY01) This product (E‐SY01) is expected to be used in an electromagnetic environment where radio frequency radiation disturbance is controlled.
CE Caution: Use the Product in the environment with the temperature Between -10℃ and 40℃; Otherwise, it may damage your product. Products can only be used below 2000m altitude For the following equipment: Product Name: Infusion Monitor Device Brand Name: -Model No.: E-IR500 Zhejiang Zhier Information Technology Co., Ltd. E-mail: qiliping@enjoyor.net This product is intended for sale and application in a business environment.
FCC Warning 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 1: 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.
