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Authorized Components

.

Please use the TRANSTEK 

authorized adaptor.

2

.Storage bag.

Adaptor
Type:

UE08WCP-060100SPA

Input:

100~240V

50~60Hz,400mA

Output:

6V      1A

17

16

Contact Information

(Conforms to UL certificate)

AUTHORIZED COMPONENTS

For more information about our products, please visit www.transtek.cn.you can get 

customer service, usual problems and customer download, transtek will serve you 

anytime.

Manufactured by:

GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD

Company:

GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD

Address:

Zone A, 5/F., Investment Building , No. 12, Huizhan East Rd., Torch 

Development District, Zhongshan, Guangdong, 528437, China

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.

 

Caution: The user is cautioned that changes or modifications not expressly 

approved by the party responsible for compliance could void the user’s authority 

to operate the equipment.

 

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. 

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.

FCC Radiation Exposure Statement:

This equipment complies with FCC radiation exposure limits set forth for an  

uncontrolled environment. 

This transmitter must not be co-located or operating in conjunction with any other 

antenna or transmitter.

FCC Statement

Summary of Contents for LS802-E

Page 1: ...u very much for selecting TRANSTEK Blood Pressure Monitor LS802 E please keep well this manual in order to reference in future Arm Type Version 1 0 FCC ID OU9LS802 E02 GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO LTD Zone A 5 F Investment Building No 12 Huizhan East Rd Torch Development District Zhongshan Guangdong 528437 China ...

Page 2: ...SER 10 Tips for measurement Maintenances ABOUT BLOOD PRESSURE 12 What are systolic pressure and diastolic pressure What is the standard blood pressure classification Why my blood pressure is varies even in one day Why the blood pressure I get from the hospital is different from home If the result is the same if measuring on the right arm TROUBLESHOOTING 14 SPECIFICATIONS 15 AUTHORIZED COMPONENTS 1...

Page 3: ...e START STOP button to stop inflation The equipment is not AP APG equipment and not suitable for use in the presence of a flammable anesthetic mixture with air of with oxygen or nitrous oxide The operator shall not touch output of batteries adapter and the patient simultaneously To avoid measurement errors please avoid the condition of strong electromagnetic field radiated interference signal or e...

Page 4: ...measurement for user 2 and then save the measure data Data storage To remind the users that the measurement data don t upload to bridge in time Wireless transmitter The blood monitor and Bridge in communication Network connection The bridge not connect the network Shocking remainding Shocking will result in inaccurate Low battery Batteries are low and need to be replaced Measurement Unit of the bl...

Page 5: ...ws your blood circulation to recover For a meaningful comparison try to measure under similar conditions For example take daily measurements at approximately the same time on the same arm or as directed by a physician Tie the Cuff 1 Tie the cuff on your upper arm the position the tube off center toward the inner side of arm in line with the little finger 2 The cuff should be sung but not too tight...

Page 6: ...ssful activation synchronization the equipment will display and transmit the measuring results after each measurement Activation synchroniz ation is proceeding The measureme nt data is uploading The data has been uploaded successfully CAUTION Interference may occur in the vicinity of equipment marked with the following symbol And LS802 E may interfering vicinity electrical equipment Sensitive peop...

Page 7: ... it with a dry cloth in case Avoid the dusty and unstable temperature environment Avoid washing the cuff 11 10 Tips for measurement In a very cold environment Immediate measurement after tea coffee smoking When talking or moving your fingers When you want to discharge urine It can cause incorrectness if the measurement are taken in the following circumstances Within 20 minutes after taking a bath ...

Page 8: ...LOOD PRESSURE If the result is the same if measuring on the right arm ABOUT BLOOD PRESSURE Irregular Heartbeat Detector This Blood Pressure Monitor is equipped with an intelligent function of Irregular Heartbeat IHB Detector During each measurement this equipment records the heartbeat intervals and works out the standard deviation If the calculated value is larger than or equal to 15 this equipmen...

Page 9: ...th new batteries Batteries are inserted incorrectly Display is dim or show Batteries are low E 1 shows RF communication failed Check the database is power on or not Or synchronize the data operation E 3 shows E10 or E11 shows E20 shows Exxx shows on the display A calibration error occurred Retake the measurement If the problem persists contact the retailer or our customer service department for fu...

Page 10: ...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 harm...

Page 11: ...cle processes ISO EN 14971 2012 Medical devices Application of risk management to medical devices ISO EN 15223 1 2012 Medical devices Symbols to be used with medical device labels labelling and information to be supplied General requirements EN 1041 2008 Medical equipment manufacturers to provide information IEC 60601 1 2005 A1 2012 Medical electrical equipment Part 1 General requirements for basi...

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