CardiAI BPAro Operator'S Manual Download Page 18

18

 

BPAro 

ENG Revision A

 

Application 

 

 

 

3.6

 

Switching ABPM Devices ON and 

OFF 

The ABPM devices have a power switch inside their 

battery compartment. Open the battery compartment (see 

Fig. 3.1) and turn the device on and off as follows, if 

(rechargeable) batteries have been inserted: 

To switch ON:  Slide the switch to ON. 

To switch OFF:  Slide the switch to OFF 

3.7

 

Performance Check  

When turned on, the ABPM devices run a self-test that 

includes all symbols and segments on the LCD (Fig. 

3.5). Then, the version number of the device software is 

displayed (e.g., “P 30” for version 3.0). 

Afterwards, the device checks the inserted 

(rechargeable) batteries and indicates the remaining 

capacity (see Fig. 3.6). "A 100", for instance, means that 

the rechargeable batteries have a capacity of 100%, i.e., 

they are fully charged. "b 50" means that the alkaline 

batteries have a capacity of only 50%, i.e., they are half 

depleted. 

The minimum battery capacity for a 24-hour measure- 

ment is 90%. 

If the capacity is below 90%, new or fully charged 

batteries must be inserted. 

BP monitors that have passed the self-test and completed 

the battery test will indicate the following information: 

 

the time of day 

 

the measuring phase (day        / night        ), and 

 

whether data are stored in the BP monitor (

M

) (see 

Fig. 3.7). 

The BP monitor will also emit an audio signal if enabled. 

 

 

 

    Fig. 3.5  Test display on LCD

 

 

 

   Fig. 3.6  Battery capacity of 80 %

 

 

3.8

 

Clock Display 

Each time the device is started by the PC software, the 

clock, which is integrated into the device, is auto-

matically set to the PC time (see Fig. 3.7). Manually 

changing the time at the device is not possible.   

 

      Fig. 3.7  Example: Display after successful self-test 

(= BP data in memory,         measuring 

phase: day)

 

 

Summary of Contents for BPAro

Page 1: ...BPAro Ambulatory Blood Pressure System Firmware Version 3 0 Operator s Manual A8135 ENG Revision A...

Page 2: ...please inform us so that we can resolve the discrepancies as soon as possible Due to continuing product innovation specifications in this manual are subject to change without notice To find out about...

Page 3: ...NiMH batteries 16 3 5 Charging Batteries with the VARTA Charging Unit 17 3 6 Switching ABPM Devices ON and OFF 18 3 7 Performance Check 18 3 8 Clock Display 18 4 Application 19 4 1 Applying the cuff...

Page 4: ...Aro ENG Revision A General Information 6 5 Disposal of the Product 25 7 Technical Specifications 26 7 1 Blood Pressure Measurement 26 8 Order Information 27 9 Appendix Electromagnetic Compatibility EM...

Page 5: ...vision History This manual is subject to change order service The revision index a letter that follows the order number changes with every update of the manual Order Number Revision Date Comment A8135...

Page 6: ...ance of the information given in the manual is a prerequisite for proper equipment performance and correct operation and ensures patient and operator safety Please note that information pertinent to s...

Page 7: ...7 BPAro ENG Revision A General Information CardiAI Inc 201 3151 27th St NE Calgary Alberta T1Y 0B4 Canada www cardiai com The country of manufacture is indicated on the device label...

Page 8: ...ence The cuffs are wrapped around the uninjured upper arm so that they come in contact only with intact skin The devices are not intended to be used in intensive care medicine or for raising alarm in...

Page 9: ...ic value Once the systolic value is determined the cuff can immediately and quickly be deflated The measurement typically takes only approx 20 seconds See Fig 1 2 If disturbances occur during measurem...

Page 10: ...result of the proposed combination of equipment The standards IEC 60601 1 or IEC 60950 1 must be observed in any case Connection of this device to an IT network that includes other equipment could res...

Page 11: ...EMC requirements X ray equipment MRI devices radio systems etc are possible sources of interference as they may emit higher levels of electromagnetic radiation Caution Equipment damage risk to person...

Page 12: ...During a long term measurement the buttons on the device have the following functions To start and stop a measurement and to confirm entries To display the most recent measurement values or error mess...

Page 13: ...hases is only possible if two measure intervals were programmed when the ABPM device was started with the PC software and the day night button has not been deactivated If more or less than two measure...

Page 14: ...hase selected Night phase selected Further relevant symbols used on the battery charger Eurasian Conformity Conformity with the current technical regulations of the Customs Union Protection class II e...

Page 15: ...of operation or 400 blood pressure measurements The capacity of rechargeable batteries decreases with age If the capacity of fully charged batteries is consider ably less than 24 hours the batteries...

Page 16: ...arity when inserting the batteries Note The energy source needs to be selected only when the BP monitor is put into service for the first time or when you change from NiMH to alkaline batteries and vi...

Page 17: ...r in the charging unit display where each symbol corresponds to one of the charger compartments Fig 3 4 During the charge cycle the corresponding bar in the battery sym bols blinks Note If the battery...

Page 18: ...have a capacity of 100 i e they are fully charged b 50 means that the alkaline batteries have a capacity of only 50 i e they are half depleted The minimum battery capacity for a 24 hour measure ment...

Page 19: ...to the patient due to blood flow interference The application of the cuff over a wound can cause further injury The application of the cuff and its pressurization on the arm on the side of a mastecto...

Page 20: ...onnect it to the blood pressure cuff port of the ABPM device see Fig 2 3 Do not wrap the pressure tubing completely around the neck to avoid strangulation of the patient You must hear the connector cl...

Page 21: ...remove the pressure hose only in emergency situations see warning below that the cleaning may only be carried out by qualified medical personnel and not by the patient Absolute contraindications The...

Page 22: ...e inflates the cuff to a pressure which is 25 mmHg above the systolic value of the previous measurement minimum inflation pressure 120 mmHg The determination of the blood pressure values takes place w...

Page 23: ...on measurement method Tighten the cuff so that one finger but not two can be inserted between the patient s arm and the cuff At the same time the device switches to a deflation rate of 4 mmHg s When i...

Page 24: ...idin Foam or equivalent disinfectants that are used in practices or hospitals are suitable Please respect the information of the manufacturer especially regarding the exposure time After cleaning rins...

Page 25: ...uest CardiAI provides a Service Manual The device does not require any other maintenance Technical Inspections of the Measuring System The non invasive pressure measurement system of the ABPM devices...

Page 26: ...tion atmospheric pressure 500 1060 hPa altitude relative to sea level 400 4500 m Protection Class IP20 ABPM device IP02 wearable pouch of the ABPM device IP22 ABPM device in wearable pouch Expected Se...

Page 27: ...ith D ring A 2535 xl BPAro BP Cuff for Adults Extra Large 38 46 cm with D ring Operator Manuals USB flash drive Optional Accessories and Combinable Medical Products A 2535 s BPAro BP Cuff cuff for adu...

Page 28: ...issions to EN 55011 CISPR 11 Group 1 The ABPM devices use RF energy only for their internal function Therefore their RF emissions are very low and are not likely to cause any interference in nearby el...

Page 29: ...ommercial or hospital environment Surge to EN 61000 4 5 IEC 61000 4 5 0 5 kV differential mode 1 0 kV differential mode 0 5 kV common mode 1 0 kV common mode 2 0 kV common mode not applicable not appl...

Page 30: ...nd d is the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electro magnetic site surveya should be less than the compli ance level in each f...

Page 31: ...Power of Transmitter W Separation Distance According to Frequency of Transmitter m 150 kHz to 80 MHz d 1 17 P 80 MHz to 800 MHz d 1 17 P 800 MHz to 2 7 GHz d 2 33 P 0 0 1 0 1 2 0 1 2 0 2 4 0 1 0 3 7...

Page 32: ...om the wearable pouch Please wear the pouch over your clothes You do not have to clean the device after the long term measurement Sometimes the device internally stops the long term measurement In thi...

Page 33: ...33 BPAro ENG Revision A CardiAI Inc 201 3151 27th St NE Calgary Alberta T1Y 0B4 Canada www cardiai com...

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