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Summary of Contents for Cor1

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Page 5: ...Number Manufacturer Direct Current Manufacture Date Type B Applied Parts ENVIRONMENT PROTECTION Waste electrical products should not be disposed of with house hold waste Please recycle where facilities exist Check with your local authority or retailer for recycling advice Caution ...

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Page 8: ...ats per Minute Memory See Page 14 Movement Error Results in Inaccurate Measurement Low Battery Replace Batteries kPa Measurement Unit 1kPa 7 5mmHG mmHg Measurement Unit 1mmHg 0 133kPa Deflating Cuff is Deflating Current Time YY MM DD HH MM Grade Grade of Blood Pressure Arrhythmia Irregular Heartbeat Heartbeat Heartbeat Detection During Measurement N ...

Page 9: ...Norm Hype G3 G2 G1 Time Date Memory Pul min Hypo ...

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Page 22: ...press artery vein blood discharging Systolic relax blood entering Diastolic ...

Page 23: ...ive 120 139 or 80 89 High Blood Pressure Stage 1 Hypertension Hypertension Stage 1 140 159 or 90 99 High Blood Pressure Stage 2 Hypertension Hypertension Stage 2 160 or higher or 100 or higher Hypertensive Crisis Emergency Care Needed Emergency Care Needed Higher than 180 or Higher than 110 SYS 135 mm Hg DIA 85 mm Hg ...

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Page 26: ...e pressure of the cuff is excessive Relax for a moment then measure again E10 or E11 Shows The monitor detected motion while measuring Movement can affect the measurement Relax then measure again E20 Shows The measurement process does not detect the pulse signal Loosen clothing on the arm and them measure again E21 Shows Measure incorrectly Relax for a moment and then measure again EExx shows on t...

Page 27: ...a to 105kPa Storage transportation condition Temperature 24 8 F to 131 F Temperature 20 C to 55 C Relative humidity 90 RH Measurement perimeter of the wrist Approximately 5 3 in 8 4 in Approximately 13 5 cm 21 5 cm Weight Approximately 4 23 oz Excluding the dry cells External dimensions Approx 2 6 in x 2 9 in x 1 2 in 68 mm 75 mm 31mm Attachment 2 AAA batteries user manual Mode of operation Contin...

Page 28: ...ity Requirements and tests Performance and clinical requirements ANSI AAMI SP10 2002 A2 2008 Manual electronic or automated Software life cycle processes IEC 62304 2006 AC 2008 Medical device software Software life cycle processes Guidance and manufacturer s declaration electromagnetic emission The device is intended for use in the electromagnetic environment specified below The customer or the us...

Page 29: ...tter m 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz 0 01 Not Applicable 0 117 0 233 0 1 Not Applicable 0 369 0 738 1 Not Applicable 1 167 2 333 10 Not Applicable 3 690 7 378 100 Not Applicable 11 67 23 33 For transmitters rated at a maximum output power not listed above the recommended separation distance d in meters m can be estimated using the equation applicable to the frequency of th...

Page 30: ...00 4 5 1 kV line s to line s 2 kV line s to earth N A Mains power quality should be that of a typical commercial or hospital environment Voltage dips short interruptions and voltage variations on power supply input lines IEC 61000 4 11 5 UT 95 dip in the UT for 0 5 cycles N A Mains power quality should be that of a typical commercial or hospital environment If the user of the device requires conti...

Page 31: ...y should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Field strengths from fix...

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