Related Manuals for B.Well PRO-36
Summary of Contents for B.Well PRO-36
- Page 1 Instruction for use PRO-36 Automatic blood pressure monitor High-accuracy measurements...
-
Page 3: Table Of Contents
Instruction for use PRO-36 Model PRO-36 Automatic Upper Arm Blood Pressure Monitor Instruction for Use INDEX 1. INTRODUCTION ...................................4 2. IMPORTANT INFORMATION ON THE SUBJECT OF BLOOD-PRESSURE AND ITS MEASUREMENT ....4 2.1. Normal blood pressure fl uctuation..........................4 2.2. Classifi cation of blood pressure values ........................5 3. -
Page 4: Introduction
This device is easy to use and has been proven in clinical studies to provide excellent accuracy. Before using the PRO-36, read this instruction manual carefully and keep it in a safe place. For further questions on the subject of blood-pressure and its measurement, please contact your doctor. -
Page 5: Classification Of Blood Pressure Values
Instruction for use PRO-36 Considering the above information, it is recommended that you measure your blood pressure at approximately the same time each day. Too frequent measurements may cause injury due to blood fl ow interference, please always relax a minimum moment of 1 to 1.5 minutes between measurements to allow the blood circulation in your arm to recover. -
Page 6: Contents And Display Indicators
Instruction for use PRO-36 3. CONTENTS AND DISPLAY INDICATORS Cuff Air tube socket Air tube Systolic Pressure LCD Display Diastolic Pressure Pulse Rate Voice expanding holes Power adapter socket Heart beat symbol Volume knob Zero-seeking symbol Start button Low battery symbol... -
Page 7: Precautions
Instruction for use PRO-36 6. PRECAUTIONS 1. Read all of the information in the operation guide and any other literature in the box before operating the unit. 2. Stay still, calm and rest for 5 minutes before blood pressure measurement. -
Page 8: Setup And Operating Procedures
Instruction for use PRO-36 The monitor might not meet its performance specifi cations or cause safety hazard if stored or used outside the specifi ed temperature and humidity ranges in specifi cations. Please do not share the cuff with other infective person to avoid cross-infection. -
Page 9: Using A Mains Adapter
Instruction for use PRO-36 The monitor, the batteries and the cuff, must be disposed of according to local regulations at the end of their usage. 7.2. Using a mains adapter 1) Plug the mains adaptor into a 100-240 V, 50/60Hz power socket. -
Page 10: Carrying Out A Measurement
Instruction for use PRO-36 c. While seated, place palm upside in front of you on a fl at surface such as a desk or table. Position the air tube in the middle of your arm in line with your middle fi nger. -
Page 11: Taking Your Blood Pressure Reading
Instruction for use PRO-36 Common sources of error: Note: Comparable blood-pressure measurements always require the same conditions! These are normally always quiet conditions. All efforts by the patient to support the arm can increase the blood-pressure. Make sure you are in a comfortable, relaxed position and do not activate any of the muscles in the measurement arm during the measurement. -
Page 12: Pulse Arrhythmia Detection
During measurement, you can press the “START” button to turn off the monitor manually. The device then immediately lowers the cuff-pressure automatically, and you will hear at the time “B.Well wishes you all the best – stay healthy!” Note: Please consult a health care professional for interpretation of pressure measurements. -
Page 13: Troubleshooting (1)
Instruction for use PRO-36 7.10. Troubleshooting (1) PROBLEM POSSIBLE CAUSE SOLUTION The cuff position was not correct or it was not Apply the cuff correctly and try again properly tightened Review the “BODY POSTURE DURING MEASURE- Body posture was not correct during testing MENT”... -
Page 14: Maintenance
Instruction for use PRO-36 LCD shows “Er 5” Cuff pressure above 300mmHg More than 3 minutes with cuff pressure above LCD shows “Er 6” 15 mmHg Measure again after fi ve minutes. If the monitor is still abnormal, please contact the local distributor or LCD shows “Er 7”... -
Page 15: Specifications
9. SPECIFICATIONS 1. Product name: Blood Pressure Monitor 2. Model: PRO-36 3. Classifi cation: Internally powered, Type BF applied part, IPX0, No AP or APG, Continuous operation 4. Machine size: 87mm x 122mm x 53mm (3 7/16" x 4 13/16" x 2 3/32") 5. -
Page 16: Applied Standards
Instruction for use PRO-36 10. APPLIED STANDARDS The digital automatic blood pressure monitor corresponds to the below standards: IEC 60601-1:2005/EN 60601-1:2006/AC:2010 (Medical electrical equipment – Part 1: General requirements for basic safety and essential performance), IEC60601-1-2:2007/EN 60601-1-2:2007 /AC:2010 (Medical electrical equipment – Part 1-2: General requirements for basic safety and essential performance –... -
Page 17: Warranty Information
Instruction for use PRO-36 POLARITY OF D.C. POWER CONNECTOR OPERATING CONDITION, TEMPERATURE 10˚C ~ 40˚C STORAGE CONDITION, TEMPERATURE –20˚C ~ 50˚C KEEP DRY 12. WARRANTY INFORMATION Warranty period is 3 years from the date of purchase for monitor and 1 year for cuff and adapter. This warranty doesn’t cover any dam- ages caused by improper using, and also battery, and packaging. -
Page 18: Electromagnetic Compatibility Information
Guidance and manufacturer’s declaration – еlectromagnetic emissions The PRO-36 is intended for use in the electromagnetic environment specifi ed below. The customer or the user of the PRO-36 should assure that it is used in such an environment. Emissions test... - Page 19 Guidance and manufacturer’s declaration – еlectromagnetic immunity The PRO-36 is intended for use in the electromagnetic environment specifi ed below. The customer or the user of the PRO-36 should assure that it is used in such an environment. Immunity test...
- Page 20 For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING Guidance and manufacturer’s declaration – electromagnetic immunity The PRO-36 is intended for use in the electromagnetic environment specifi ed below. The customer or the user of the PRO-36 should assure that it is used in such an environment.
- Page 21 fi xed RF transmitters, an electromagnetic site survey should be considered. If the measured fi eld strength in the location in which the PRO-36 is used exceeds the applicable RF compliance level above, the PRO-36 should be observed to verify normal operation.
-
Page 22: Latest Revision
Instruction for use PRO-36 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 the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. - Page 24 B.Well Swiss AG Bahnhofstrasse 24, CH-9443 Widnau, Switzerland...
Need help?
Do you have a question about the PRO-36 and is the answer not in the manual?
Questions and answers