Instruction Manual
Table Of Contents
- FCC Statement
- 1. Introduction
- 1.1. Product Introduction
- 1.2. Safety Guide
- 1.3. Symbol and text description
- 2. Recommended clinical application
- 3. Product Description
- 3.1. Standard Configuration
- 3.2. Product Introduction
- 3.3. Main interface (monitoring interface) descrip
- 3.4. Setting interface specification
- 4. Setting of monitor
- 4.1. Disassembly and installation and list of acce
- 4.2. Connect the power supply Charge
- 5. Operational Guidelines
- 5.1. Preparation before Use
- 5.2. FHR monitoring
- 5.3. TOCO monitoring
- 5.4. Manual FM monitoring
- 5.5. Monitoring information update
- 5.6. Restore Factory Settings
- 6. Maintenance and clean of Fetal Monitor
- 6.1. Product Handling
- 6.2. Maintenance
- 6.3. Cleaning and Disinfection
- 6.4. Gel
- 7. Packaging, transportation and storage
- 7.1. Packaging
- 7.2. Transport
- 7.3. Storage
- 8. Fault finding and eliminating
- 9. Warranty Period and Maintenance
- 10. Technical Parameters
- AppendixⅠ—Electromagnetic Compatibility Declaratio
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AppendixⅠ—Electromagnetic Compatibility Declaration
This device is capable of generating, using, and radiating RF energy. This equipment may cause the
electromagnetic interference between other medical devices or non-medical devices, as well as radio communications.
According to the statement of IEC 60601-1-2, this product belongs to the medical device with the emission limit of
B-grade in first group, so as to provide corresponding protection measures for avoiding interference. Nevertheless, it
cannot be fully guaranteed that the electromagnetic interference will not occur under specific installation conditions.
When it is discovered that this equipment causes an interference phenomenon, (it needs to be confirmed by the
switch-on and switch-off of the equipment), the operators (or the maintenance personnel) can eliminate the
interferences based on the following measures:
Adjust or reposition the affected device;
Increase the distance between the device and the affected device;
Use another power supply to provide power for the device;
Consult maintenance engineers for more advice.
Note: Before using this device, please make sure that all of the requirements for EMC in this section are met.
Note: This Chapter shall list the contents described in IEC 60601-1-2, and the users are obliged to ensure that
this equipment and its nearby equipment conform to the RF interference parameters as indicated in the
general safety requirements.
Note: Near this device, do not using the devices that purposely transmit RF signals (mobile phones, radio
receiver and transmitter or radio controlled products), for this may cause operation to exceed the
specified values. When it is near this device, please switch off such types of the device. The operator
shall have the responsibility to prompt the patient or other personnel near the device to comply fully
with the above requirements.
Note: The manufacturer will not be responsible for any interference caused by the use of non-recommended
internal connecting cables or any unauthorized changes or modifications to this equipment.
Guidance and manufacturer’s declaration – electromagnetic emissions
The JPD-300E is intended for use in the electromagnetic environment specified below. The
customer or the user of the JPD-300E should assure that it is used in such an environment.
Emissions test
Compliance
Electromagnetic