Prolife PS1 Standard Instruction Manual
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Prolife PS1 Standard Instruction Manual

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DIGITAL
BLOOD PRESSURE MONITOR
Prolife PS1 Standard
en
Instruction manual

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Summary of Contents for Prolife PS1 Standard

  • Page 1 DIGITAL BLOOD PRESSURE MONITOR Prolife PS1 Standard Instruction manual...

  • Page 2: Medical Device Description

    Digital Blood Pressure Monitor Prolife PS1 Standard. MEDICAL DEVICE DESCRIPTION The Digital Blood Pressure Monitor Prolife PS1 Standard is a semi-automatic digital blood pressure measuring device for use on the upper arm (with inte- grated date /time display), which enables very fast and reliable measurement of the systolic and diastolic blood pressure as well as the pulse frequency.
  • Page 3 Electrical shock protection Internal power unit Safety classifications Type BF equipment Mode of operation Continuous operation Protection against ingress of IP22 water Prolife standard cuff 22–32 cm with a pump ball, Accessories 4 size AA batteries, instruction manual, warranty card...
  • Page 4 COMPLETENESS Cuff connection opening TIME button ON/OFF button MEMORY button Display Time and date User selection Traffic light display Systolic value Pressure units Diastolic value Memory set number Heart symbol Air pump-up Pulse Air discharge Memory symbol Heart arrhythmia Battery warning symbol indicator...

  • Page 5: Inserting The Batteries

    PUTTING THE DIGITAL BLOOD PRESSURE MONITOR INTO OPERATION Inserting the batteries 1. Insert the batteries (4 x size AA, 1.5 V), thereby observing the indicated polarity. 2. If the battery warning , icon appears in the display, the batteries are empty and must be replaced by new ones. ATTENTION After the battery warning , icon appears, the device is blocked until...
  • Page 6 Setting the time and date This blood pressure monitor incorporates an integrated clock with date display. This has the advantage, that at each measurement procedure, not only the blood- pressure values are stored, but also the exact moment of the measurement. After new batteries have been inserted, the clock begins to run from 12:00, after pressing the TIME button –...

  • Page 7: Further Information

    5. Press the TIME button again. The display now switches to the current time, during which the first character (hour) blinks. The corresponding hour can now be entered by pressing the MEMORY button. 6. Press the TIME button again. The last two characters (minutes) now blink. The exact time can now be entered by pressing the MEMORY button.
  • Page 8 The performance of an automatic sphygmomanometer can be influ- enced by extreme environmental conditions: high or low temperature, humidity, elevation of the measurement point above sea level. • Prevent deformation and twisting of the cuff tube. • Improper (loose) fixation of the cuff on the arm causes false measure- ment values.

  • Page 9: Measuring Procedure

    3. Keep your legs straight and uncrossed, lean on the back of the chair. Measuring procedure After the cuff has been appropriately positioned, the measurement can begin: 1. Press ON/OFF button to switch on the device and wait until «0» appears in the display and the arrow starts to flash.

  • Page 10: Memory Full

    4. When the measurement has finished, press the quick discharge valve in order to release any remaining air in the cuff. Discontinuing a measurement If it is necessary to interrupt a blood pressure measurement for any reason (e. g. the patient feels unwell), the ON/OFF button can be pressed at any time.

  • Page 11: Appearance Of The Heart Arrhythmia Indicator For Early Detection

    In order to delete all stored readings, depress the MEMORY button for at least 5 seconds, the display will show the symbol «CL»and then release the button. The symbol «CL» begins to blink. To permanently clear the memory, press the MEMORY button while «CL» is flashing. APPEARANCE OF THE HEART ARRHYTHMIA INDICATOR FOR EARLY DETECTION This symbol indicates that certain pulse irregularities were detected...
  • Page 12 The measured readings indicated an unacceptable difference between systolic and diastolic pressures. Take another reading following directions carefully. Contact you doctor if you continue to get unusual readings The pressure is over 290 mm Hg Other possible malfunctions and their elimination If problems occur when using the device, the following points should be checked and if necessary, the corresponding measures are to be taken: Malfunction...
  • Page 13 Further Information • The level of blood pressure is subject to fluctuations even with healthy people. Important thereby is, that comparable measurements always require the same conditions (Quiet conditions)! If, in spite of observ- ing all these factors, the fluctuations are larger than 15 mmHg, and / or you hear irregular pulse tones on several occasions, please consult your doctor.
  • Page 14 Which values are normal? The blood pressure is considered to be elevated, if at rest the diastolic pressure level is 90 mmHg or above and/or the systolic pressure level is above 140 mmHg. In this case, please consult your doctor. Maintenance of such pressure levels for a long period of time pose risk to health.
  • Page 15 The Digital Blood Pressure Monitor Prolife PS1 Standard is intended for use in the electromagnetic environment specified below. The customer or the user of the Prolife PS1 Standard should assure that it is used in such an environment. Electromagnetic emissions: (IEC 60601-1-2)
  • Page 16 IEC 61000-4-11 eration during power mains for 5 cycles interruptions, it is recom- 70 % UT mended that the Prolife PS1 (30 % dip in UT) Standard be powered from for 25 cycles an uninterruptible power supply or a battery <5 % UT...
  • Page 17 Portable and mobile RF IEC 61000-4-6 to 80 MHz communications equipment 80 % AM (2 Hz) should be used no closer to any part of the Prolife PS1 Standard, including cables, Radiated RF 3 Vrms 80 MHz 3 V/m than the recommended sep- IEC 61000-4-3 to 2.5 GHz 80 %...
  • Page 18 To assess the electromagnetic environment due to fixed RF trans- mitters, an electromagnetic site survey should be considered. If the meas- ured field strength in the location in which the Prolife PS1 Standard is used exceeds the applicable RF compliance level above, the Prolife PS1 Standard should be observed to verify normal operation.

  • Page 19: Care And Maintenance

    • It is forbidden to open the device housing and perform any other indi- vidual manipulations! WARRANTY The Digital Blood Pressure Monitor Prolife Prolife PS1 Standard a 10 years warranty from the date of purchase. The warranty does not apply to damage caused by improper handling, accidents, not following the operat- ing instructions or alterations made to the device by third parties.

  • Page 20: Service Life

    The manufacturer reserves the right to make changes in the design of the device. The information of the date of mass production and the importer is placed on the individual package. SERVICE LIFE The service life of the device is 10 years. BATTERY LIFE It is used 1000 times measurement with 4 size AA alkaline batteries.

  • Page 21: Reference To Standards

    For this device you can use such models of cuffs as: Prolife standard cuff 22–32 cm; Prolife standard cuff 22–42 cm; Prolife conic cuff 22–42 cm. Device care Clean the device only with a soft, dry cloth. Disposal The symbol on the product or on its packaging indicates that this prod- uct is not classified as household waste.
  • Page 22 "IG Trend" LLP, Republic of Kazakhstan, Almaty, Rayymbek Avenue, No. 169, tel +7 727 339-3474, e-mail: info@igtrend.kz For service support on the territory of the Republic of Kazakhstan, please call +7(701) 035 1445 or email: service@igtrend.kz Prolife® is the registered trademark by Montex Swiss AG, Tramstrasse 16, CH–9442, Berneck, Switzerland.

  • Page 23: List Of Symbols

    LIST OF SYMBOLS Symbol Meaning The product complies with Directive 93/42/EEC concerning med- ical products. WEEE (Waste Electrical and Electronic Equipment Directive). The symbol on the product or its package means that this prod- uct does not fall under the category of domestic waste. To avoid possible damage to the environment and human health, separate such wastes from others and dispose of them in accordance with accepted standards.

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