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Using wet cloths to remove dirt

 

Do not attempt to clean the reusable 

cuff with water and never immerse the 

cuff in water.

Disinfection:

 If required (for example, in a hospital setting), disinfection of 

the pressure cuff twice per week is recommended.

Disinfect the interior of the pressure cuff (the surfaces that come into con

-

tact with the patient’s skin) with the use of a soft cloth soaked in ethyl 

alcohol (75-90%) and wait for the pressure cuff to dry up.

Cleaning of the pressure cuff after 200 uses is recommended.

Periodic calibration of device:

 the accuracy of measurement instru-

ments must be verified from time to time. For this reason, verification of 

the indication of statistical pressure periodically (once a year) and after 

technical maintenance and repair is recommended. More information can 

be obtained from the service center.

SYMBOL INFORMATION 

SYMBOL

REFERENT

Consult instruction for use

Manufacturer

Manufacturing date

Summary of Contents for iCare

Page 1: ...automatic BLOOD PRESSURE MONITOR model iCare MONITOR m mo od de el l i iC Ca ar re e...

Page 2: ...r blood pressure and pulse correctly For all questions concerning the de vice please contact your local distributor or TM iHerz service centre in your country ATTENTION This blood pressure monitor is...

Page 3: ...pushing blood into the arteriae and a diastolic lower one which means the blood pressure between two heartbeats Blood pressure is subject to fluctuations during the day even in healthy people The fluc...

Page 4: ...e optimum 100 119 60 79 Blood pressure normal 120 129 80 84 Blood pressure slightly high 130 139 85 89 Blood pressure too high 140 159 90 99 Blood pressure far too high 160 179 100 109 Blood pressure...

Page 5: ...rement there appears the dotted line in the left part of the display opposite the zone to which the result of the measurement corresponds green zone optimal blood pressure yellow elevated orange too h...

Page 6: ...received a mastectomy Please consult your doctor prior to using the unit if you suffer from illnesses The device is not suitable for measuring the blood pressure of children Ask your doctor before usi...

Page 7: ...n of the cuff and its pressurization on any arm where intravascular access or therapy or an arterio venous A V shunt is present inflating the cuff on the side of a mastectomy Warning Do not apply the...

Page 8: ...n This device comprises sensitive components and must be treated with caution Observe the storage and operating conditions described in this booklet The equipment is not AP APG equipment and not suita...

Page 9: ...ded that the performance should be checked every 2 years and after maintenance and repair by retesting at least the requirements in limits of the error of the cuff pressure indication and air leakage...

Page 10: ...ect this equipment and should be kept at least a distance d away from the equipment The distance d is caculated by the MANUFAC TURER from the 80MHz to 5 8 GHz column of Table 4 and Table 9 of IEC 6060...

Page 11: ...COMPARTMENT Installing and Replacing the Batteries Open the battery cover Install the batteries as indicated in the battery compartment Always select the authorized specified battery Four AAA size ba...

Page 12: ...e environment Do not dispose with daily garbage Remove the old batteries from the device following your local recycling guidelines LCD display signal SYMBOL DESCRIPTION EXPLANATION Systolic blood pres...

Page 13: ...is important to set the clock before using your blood pressure monitor so that a time stamp can be assigned to each record that is stored in the memory The setting range of the year 2014 2054 time for...

Page 14: ...middle of the cuff should be at the level of the right atrium of the heart Efforts by the patient to support the arm can increase the blood pres sure Make sure you are in a comfortable relaxed positio...

Page 15: ...2 cm above the bend of your elbow on the inside of your left arm Identify where the pulse can be felt the strongest This is your main artery 4 The cuff should be snug but not too tight You should be...

Page 16: ...he monitor and it will finish the whole measurement Take User 1 for example Press the START STOP to power off otherwise it will turn off within 1 minute MEMORY FUNCTION Reading Measurement Results 1 W...

Page 17: ...If you did not get the correct measurement you can delete all results by following steps below 1 Hold pressing MEM SET for 3 seconds when the monitor is in the memory recall mode the flash display wil...

Page 18: ...he cuff is too tight or too loose Readjust the cuff not too loose or too tight and then measure again E 3 shows The pressure of the cuff is excess Relax for a moment and then measure again E 10 or E 1...

Page 19: ...at least 1 m away In cases where this is inevitable please make sure that the device is working properly before use If you are suffering from a heartbeat disorder arrhythmia evaluation of measurement...

Page 20: ...se of a soft cloth soaked in ethyl alcohol 75 90 and wait for the pressure cuff to dry up Cleaning of the pressure cuff after 200 uses is recommended Periodic calibration of device the accuracy of mea...

Page 21: ...network of industry funded systems for recycling the packaging materials of consumer goods TECHNICAL SPECIFICATIONS Power supply Battery powered mode 6VDC 4 AAA batteries Display mode Blue LCD with wh...

Page 22: ...AAA batteries user manual Mode of operation Continuous operation Degree of protection Type BF applied part Protection against ingress of water IP21 It means the device could protected against solid fo...

Page 23: ...d essential performance EN 60601 1 11 2015 IEC 60601 1 11 2015 Medical electrical equipment Part 1 11 General requirements for basic safety and essential performance Collateral standard Requirements f...

Page 24: ...Evaluation and testing within a risk management process ISO 10993 5 2009 Biological evaluation of medical devices Part 5 Tests for in vitro cytotoxicity ISO 10993 10 2010 Biological evaluation of medi...

Page 25: ...lies buildings used for domestic purposes Harmonic emissions IEC 61000 3 2 Class A Voltage fluctuations flicker emissions IEC 61000 3 3 Complies Table 2 Guidance and manufacturer s declaration electro...

Page 26: ...ase at 0 0 UT 300 cycle Mains power quality should be that of a typical com mercial or hospital environment Power frequency 50Hz 60Hz magnetic field IEC 61000 4 8 30 A m 50Hz 60Hz 30 A m 50Hz 60Hz Pow...

Page 27: ...of the transmitter Recommended separation distances d 0 35 P d 1 2 P Radiated RF IEC 61000 4 3 10V m 80 Am at 1kHz 10V m 80 Am at 1kHz 80 MHz to 800 MHz d 1 2 P 800 MHz to 2 7 GHz d 2 3 P where P is...

Page 28: ...nt and the device The device is intended for use in an electromagnetic environment in which radi ated RF disturbances are controlled The customer or the user of the device can help prevent electromagn...

Page 29: ...4 3 Test specifica tions for ENCLO SURE PORT IMMU NITY to RF wireless commu nications equipment Test Frequency MHz Band a MHz Service a Modula tion b Modu lation b W Dis tance m IMMU NITY TEST LEVEL V...

Page 30: ...e services only the uplink frequencies are included b The carrier shall be modulated using a 50 duty cycle square wave signal c As an alternative to FM modulation 50 pulse modulation at 18 Hz may be u...

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