Biolight Meditech WBP100, WBP201 User Manual

Electronic Sphygmomanometer
Users Manual
Guangdong Biolight Meditech Co., Ltd.
Electronic Sphygmomanometer Users manual
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Contents
1 Intended Use ......................................................................................................................... 1
2 Application ............................................................................................................................ 1
3 Safety Information ................................................................................................................ 1
4 Appearance ........................................................................................................................... 4
5 Display .................................................................................................................................. 6
6 Setting ................................................................................................................................... 7
7 Historical data review function ............................................................................................. 8
8 Download And Install The Software ..................................................................................... 8
9 Using Steps ........................................................................................................................... 8
10 Maintenance and Cleaning .............................................................................................. 11
11 Accessory and Specifications .............................................................................................. 12
12 Troubleshooting .............................................................................................................. 14
13 Equipment Symbols ........................................................................................................ 15
14 Blood pressure general knowledge ................................................................................. 15
Appendix A Guidance and Manufacturer’s Declaration of EMC ................................................... 17
Electronic Sphygmomanometer Users manual
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1 Intended Use
The device is intended to measure blood pressure and pulse rate of adult. The measurement data is available for clinical reference. It can store, manage the measure data, and transmit the measuring result via wireless signal.
It is intended to be used in clinic, general ward, physical examination department and at home.
Caution:
The patient is the operator when the device is used at home or in public
areas;
The device is intended for use only by clinical professionals and in continual
attendance when its used in hospital.
2 Application
The device is reusable and intended for measuring human blood pressure and
pulse rate.
Application population
Adult.
Measurement site
Place a bare arm through the cuff and position the cuff 1-2cm above the elbow joint.
3 Safety Information
Warning
Dont take measurement immediately after smoking, drinking alcohol, coffee
and black tea, or within an hour after a meal;
Magnetic and electrical fields are capable of interfering with the proper
performance of the device. For this reason make sure that all external equipments operated in the vicinity of the device comply with the relevant EMC requirements. Mobile phone, X-ray equipment or MRI devices are a possible source of interference as they may emit higher levels of electromagnetic radiation;
The device is designed for adults and should never be used on infants,
Electronic Sphygmomanometer Users manual
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pregnant, pre-eclampic patients or people with serious arrhythmia. Consult your physician before use on children;
Don’t use the electronic sphygmomanometer in the environment containing
inflammable anesthetic gas;
Consult your physician for any of the following situations:
a) The application of the cuff over a wound or inflamed area; b) The application of the cuff on any limb with intravascular access or
therapy, or an arterio-venous (A-V) shunt;
c) The application of the cuff on the side of a mastectomy; d) Simultaneous use with other medical monitoring equipment on the same
limb; The device cannot be used together with high-frequency electrotomes and
defibrillators;
Please do not use the device while it is charging; Please do not measure immediately after an intense movement or a bath; This product might not meet its performance specifications if stored or used
outside the specified temperature, humidity and altitude ranges;
Please do not share the cuff with any infectious person to avoid
cross-infection;
Battery replacement should only be performed by personnel who have been
confirmed qualified by the manufacturer. To do otherwise will void your warranty and possible damage your unit;
Any form of modification to this device is forbidden.
Caution
Make sure that the appropriate cuff size is used; Cuff is replaceable and its replacement can only be conducted by
manufacturer.
We recommend the users to use the original manufactured cuff and adapter.
If not, it might cause measurement error or product failure;
If the adapter is abnormal, please change the adapter;Too high cuff pressure or too long charging time may make users feel
uncomfortable, and cause ischemia and neuropathy. Please turn off the device in time and take off the cuff;
The device and adapter should be considered as a medical system. The power
Electronic Sphygmomanometer Users manual
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adapter must be provided or designated by manufacturer (see optional item list). If use another power adapter, it should be verified, otherwise electric shock may occur and cause patient death;
The effective wireless transmission distance is 5m in a barrier-free
environment. If more than this distance, the product might not work. Please use this product within effective wireless transmission distance;
The charging cable should be put beyond children to avoid the danger of
strangulation;
If children or pets beat, throw or tramp on the device, it might affect the
performance of the device. Please put the device beyond children and pets;
The main unit, cable, battery and cuff must be disposed according to the
local regulations at the end of their usage.
Caution
Changes or modifications not expressly approved by the party responsible
for compliance could void the user’s authority to operate the equipment;
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. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation;
If this equipment does cause harmful interference to radio or television
reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:
-- Reorient or relocate the receiving antenna.
-- Increase the separation between the equipment and receiver.
-- Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
-- Consult the dealer or an experienced radio/TV technician for help.
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