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Blood pressure measurements determined with MW701f are equivalent to those obtained by a trained observer using cuff/stethoscope auscultation method, within the limits prescribed by the American National Standard, Electronic or Automated Sphygmomanometers. This unit is to be used by adult consumers in a home environment. The patient is an intended operator. Do not use this device on infants or neonates. MW701f is protected against manufacturing defects by an established International Warranty Program. For warranty information, you can contact the manufacturer, Rossmax International Ltd.
Attention: Consult the accompanying documents. Please read this manual carefully before use. For specific information on your own blood pressure, contact your physician. Please be sure to keep this manual.
This unit uses the oscillometric method to detect your blood pressure. Before the cuff starts inflating, the device will establish a baseline cuff pressure equivalent to the air pressure. This unit will determine the appropriate inflation level based on pressure oscillations, followed by cuff deflation.
During the deflation, the device will detect the amplitude and slope of the pressure oscillations and thereby determine for you the systolic blood pressure, diastolic blood pressure, and pulse.
This Blood Pressure Monitor complies with the European regulations and bears the CE mark "CE 1639". The quality of the device has been verified and conforms to the provisions of the EC council directive 93/42/EEC (Medical Device Directive), Annex I essential requirements and applied harmonized standards.
EN 1060-1: 1995/A2: 2009 Non-invasive sphygmomanometers - Part 1 - General requirements
EN 1060-3: 1997/A2: 2009 Non -invasive sphygmomanometers - Part 3 - Supplementary requirements for electro-mechanical blood pressure measuring systems
EN 1060-4: 2004 Non-invasive sphygmomanometers - Part 4: Test Procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers.
ISO 81060-2:2013 Non-invasive sphygmomanometers - Part 2: Clinical investigation of automated measurement type.
This blood pressure monitor was designed for long service time. Ensure continued accuracy, it's recommended that all digital blood pressure monitors require re-calibration. This monitor (under normal usage with approx. 3 measurements a day) does not require recalibration for 2 years. Once the unit should be re-calibrated the device will display . The unit should also be re-calibrated if the monitor sustains damage due to blunt force (such as dropping) or exposure to fluids and / or extreme hot or cold temperature / humidity changes. When
appears, simply return to your nearest dealer for re-calibration service.
Refer to the definitions of the World Health Organization, the blood pressure ranges can be classified into 6 grades. (Ref. 1999 WHO-International Society of Hypertension Guidelines for the management of Hypertension). This blood pressure classification are based on historical data, and may not be directly applicable to any particular patient. It is important that you consult with your physician regularly. Your physician will tell you your normal blood pressure range as well as the point at which you will be considered at risk. For reliable monitoring and reference of blood pressure, keeping long- term records is recommended. Please download the blood pressure log at our website www.rossmax.com.
EE / Measurement Error: Make sure the L-plug is securely connected to the air socket and measure again quietly. Wrap the cuff correctly and keep arm steady during measurement. If the error keeps occurring, return the device to your local distributor or service center.
E1 / Air Circuit Abnormality: Make sure the L-Plug is securely connected to the air socket on the side of the unit and measure again quietly. If the errors still occur, return the device to your local distributor or service center for help.
E2 / Pressure Exceeding 300 mmHg: Switch the unit off and measure again quietly. If the error keeps occurring, return the device to your local distributor or service center.
E3 / Data Error: Remove the batteries, wait for 60 seconds, and reload. If the error keeps occurring, return the device to your local distributor or service center.
Er / Exceeding Measurement Range: Measure again quietly. If the error keeps occurring, return the device to your local distributor or service center.
If the cuff was wrapped too loosely, it may cause unreliable measurement results. The "Cuff Wrap Detection" can help to determine if the cuff is wrapped snugly enough. The specified icon appears once a "loosen cuff" has been detected during measurement. Otherwise the specified icon
appears if the cuff is wrapped correctly during measurement.
The "Movement Detection" helps reminding the user to remain still and is indicating any body movement during measurement. The specified icon appears once a "body movement" has been detected during and after each measurement.
Note: It's highly recommended that you measure again if the icon appears.
This monitor has a non-stored single measurement function. Press the User-Switching key to select the memory zone of guest , and follow the Measurement Procedure to take a measurement correctly. When the measurement is completed, the measurement value will not be stored in memory zone.
The World Health Organization, classifying blood pressure ranges into 6 grades. This unit is equipped with innovative blood pressure risk indication, which visually indicates the assumed risk level (optimal / normal / high-normal/ grade1 hypertension / grade 2 hypertension / grade 3 hypertension) of the result after each measurement.
This unit is equipped with an Irregular Heartbeat (IHB) Detection which allows those who have an irregular heartbeat to obtain accurate measurements alerting the user of the presence of an irregular heart beat during the measurement.
Note: It is strongly recommended that you consult your physician if the IHB icon () appears often.
You need to replace the batteries when
Here are a few helpful tips to help you obtain more accurate readings:
This blood pressure monitor will re-inflate automatically to higher pressure if the system detects that more pressure is needed to take a blood pressure measurement.
Note:
Note: The memory bank can store up to 60 readings per memory zone. When the number of readings exceeds 60, the oldest data will be replaced with the new record.
Note: AM is defined as 4:00 AM – 11:59 AM
Note: PM is defined as 6:00 PM – 2:00 AM
Rossmax provides a free, integrated and user-friendly blood pressure management software which can be downloaded and installed on your computer. You may purchase a special designed USB cable in order to connect Rossmax's blood pressure monitor and your PC. Please visit the website at http://www.rossmax.com for proceeding the downloading and installation process.
If any abnormality will arise during use, please check the following points.
Symptoms | Check Points | Correction |
No display when the ON/OFF/START key is pressed | Have the batteries run down? | Replace them with four new batteries. |
Have the batteries' polarities been positioned incorrectly? | Re-insert the batteries in the correct positions. | |
EE mark shown on display or the blood pressure value is displayed excessively low (high) | Is the cuff placed correctly? | Wrap the cuff properly so that it is positioned correctly. |
Did you talk or move during measurement? | Measure again. Keep wrist steady during measurement. | |
Did you vigorously shake the cuff during measurement? |
Note: If the unit still does not work, return it to your dealer. Under no circumstance should you disassemble and repair the unit by yourself.
Measurement Method | Oscillometric | ||
Measurement Range | Pressure: 30~260 mmHg; Pulse: 40~199 beats/ minute | ||
Pressure Sensor | Semi conductor | ||
Accuracy | Pressure: ± 3 mmHg; Pulse: ± 5% of reading | ||
Inflation | Pump Driven | ||
Deflation | Automatic Air Release Valve | ||
Memory capacity | 60 memories for each zone x 2 zones | ||
Auto-shut-off | 1 minute after last key operation | ||
Permissible Operating Temperature and Humidity | 10°C~40°C (50°F~104°F); 15%~85% RH; 700~1060 hPa | ||
Permissible Transport and Storage Temperature and Humidity | -10°C~60°C (14°F~140°F); 10%~90% RH; 700~1060 hPa | ||
DC Power Source | DC 6V four AA Batteries | ||
AC Power Source | DC 6V, ≥600mA (Plug size: outer(-) is Ø4.0, inner(+) is Ø1.7) | ||
Dimensions | 160 (L) X 120 (W) X 81 (H) mm | ||
Weight | 400g (G.W.) (w/o Batteries) | ||
Arm circumference | Adult: 24~40 cm (9.4"~15.7") | ||
Limited Users | Adult users | ||
![]() | Type BF: Device and cuff are designed to provide special protection against electrical shocks. | ||
IP Classification | IP21: Protection against harmful ingress of water and particulate matter | ||
* Specifications are subject to change without notice. |
Rossmax Swiss GmbH,
Widnauerstrasse 1, CH-9435 Heerbrugg, Switzerland
Here you can download full pdf version of manual, it may contain additional safety instructions, warranty information, FCC rules, etc.
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