Rossmax CF155f Blood Pressure Monitor User Manual

Introduction

Blood pressure measurements determined with CF155f 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. CF155f 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.

Real Fuzzy Measuring Technology

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.

Preliminary Remarks

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.

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 re-calibration for 2 years. Once the unit should be re-calibrated the device will display [re-calibration symbol]. 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 [re-calibration symbol] appears, simply return to your nearest dealer for re-calibration service.

Blood Pressure Standard

The National High Blood Pressure Education Program Coordinating Committee has developed a blood pressure standard, classifying blood pressure ranges into 4 stages. (Ref. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure-Complete Report JNC-7, 2003). 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.

Blood Pressure Standard Classification (JNC7: 2003, unit: mmHg)

Category Systolic Pressure Diastolic Pressure
Normal <120 <80
Suspected Hypertension 120~139 80~89
Suspected Stage 1 Hypertension 140~159 90~99
Suspected Stage 2 Hypertension ≥160 ≥100

Display Explanations

Key Features

Movement Detection

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.

Hypertension Risk Indication

The National High Blood Pressure Education Program Coordinating Committee has developed a blood pressure standard, classifying blood pressure ranges into 4 stages. This unit is equipped with innovative blood pressure risk Indication, which visually indicates the assumed risk level (normal / prehypertension / stage 1 hypertension / stage 2 hypertension ) of the result after each measurement.

Irregular Heartbeat (IHB) Detection

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 ( [IHB symbol] ).

Using the AC Adaptor (Optional)

  1. Connect the AC adaptor with the AC adaptor jack on the right side of the unit.
  2. Plug the AC adaptor into the socket. (AC adaptors with required voltage and current indicated near the AC adaptor jack.)

Caution:

Installing Batteries

  1. Press down and lift the battery cover in the direction of the arrow to open the battery compartment.
  2. Install or replace 4 “AAA” sized batteries in the battery compartment according to the indications inside the compartment.
  3. Replace the battery cover by clicking in the bottom hooks first, then push in the top end of the battery cover.
  4. Replace the batteries in pairs. Remove batteries when unit is not in use for extended periods of time.

You need to replace the batteries when:

Caution:

Applying the Cuff

  1. Unwrap the arm cuff, leaving the end of the cuff through the D-ring of the cuff.
  2. Put your left arm through the cuff loop. The color strip indication should be positioned closer to you with the tube pointing in the direction of your arm (Fig. ). Turn your left palm upward and place the edge of the arm cuff at approximately 1.5 to 2.5 cm above the inner side of the elbow joint (Fig. ). Tighten the cuff by pulling the end of the cuff.
  3. Center the tube over the middle of the arm. Press the hook and loop material together securely. Allow room for 2 fingers to fit between the cuff and your arm. Position the artery mark (Ø) over the main artery (on the inside of your arm) (Fig. ,). Note: Locate the main artery by pressing with 2 fingers approximately 2 cm above the bend of your elbow on the inside of your left arm. Identify where the pulse can be felt the strongest. This is your main artery.
  4. Plug in the cuff connecting tube into the unit (Fig. ).
  5. Lay your arm on a table (palm upward) so the cuff is at the same height as your heart. Make sure the tube is not kinked (Fig. ).
  6. This cuff is suitable for your use if the arrow falls within the solid color line as shown on the right (Fig. ). If the arrow falls outside the solid color line, you will need a cuff with other circumferences. Contact your local dealer for additional size cuffs.

Measurement Procedures

Here are a few helpful tips to help you obtain more accurate readings:

  1. Press the ON/OFF/START key. All displays will appear for approximately one second before returning to “0”.
  2. The unit will automatically inflate to the appropriate inflation level based on the user’s pulse oscillations. Measurement will then begin. It is important to remain still and quiet during measurement. Any significant movement may affect measurement results.
  3. When the measurement is completed, systolic, diastolic and pulse will be shown simultaneously and be saved automatically in memory system. Up to 90 memories can be saved.
  4. Measurement is now completed. Press the ON/OFF/START key to turn off the power. If no key is pressed, the unit will shut off automatically in 1 minute.

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: 1. This monitor automatically switches off approximately 1 minute after last key operation. 2. To interrupt the measurement, simply press the Memory or ON/OFF/START key; the cuff will deflate immediately.

Recalling Values from Memory

  1. To recall stored blood pressure readings from memory, simply press the Memory key, the first reading displayed is the average of the last 3 measurements stored in memory, and then the last set of memorized readings will be displayed.
  2. Another press of the Memory key will recall the previous set of readings.
  3. All readings stored in memory will be displayed with its sequence number. Every measurement comes with an assigned memory sequence number.

Clearing Values from Memory

Press and hold the Memory key for approximately 5 seconds, then the data in the memory zone can be erased automatically.

Troubleshooting

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 shake the wrist with the cuff on?

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.

Cautionary Notes

Specifications

Specification Details
Measurement Method Oscillometric
Measurement Range Pressure: 30~260 mmHg; Pulse: 40~199 beats/minute
Pressure Sensor Semiconductor
Accuracy Pressure: ± 3mmHg; Pulse: ± 5% of reading
Inflation Pump Driven
Deflation Automatic Air Release Valve
Memory capacity 90 memories
Auto-shut-off 1 minute after last key operation
Operation Environment 10°C~40°C (50°F~104°F); 40%~85% RH; 700~1060 hPa
Storage and Transportation Environment -10°C~60°C (14°F~140°F); 10%~90% RH; 700~1060 hPa
DC Power Source DC 6V four AAA Batteries
AC Power Source DC 6V, ≥600mA (Plug size: outer(-) is Ø4.0, inner(+) is Ø1.7)
Dimensions 124±2 (L) X 85±2 (W) X 68.6±2 (H) mm
Weight 222±22 g (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.

Electromagnetic Compatibility Information

1. This device needs to be installed and put into service in accordance with the information provided in the user manual.

2. WARNING: Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the CF155f, including cables specified by the manufacturer. Otherwise, degradation of the performance of this device could result.

If higher IMMUNITY TEST LEVELS than those specified in Table 9 are used, the minimum separation distance may be lowered. Lower minimum separation distances shall be calculated using the equation specified in 8.10.

Manufacturer’s declaration-electromagnetic immunity

The CF155f is intended for use in the electromagnetic environment specified below. The customer or the user of the CF155f should assure that is used in such an environment.

Immunity test IEC 60601 test level Compliance level Electromagnetic environment guidance
Conducted RF IEC 61000-4-6 3 Vrms: 0.15 MHz – 80 MHz
6 Vrms: in ISM and amateur radio bands between 0.15 MHz and 80 MHz
80 % AM at 1 kHz
3 Vrms: 0.15 MHz – 80 MHz
6 Vrms: in ISM and amateur radio bands between 0.15 MHz and 80 MHz
80 % AM at 1 kHz
Portable and mobile RF communications equipment should be used no closer to any part of the CF155f including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance: d = 1.2 √P, d = 1.2 √P 80MHz to 800 MHz, d = 2.3 √P 800MHz to 2.7 GHz Where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m).
Radiated RF IEC 61000-4-3 10 V/m
80 MHz – 2.7 GHz
80 % AM at 1 kHz
10 V/m
80 MHz – 2.7 GHz
80 % AM at 1 kHz
Interference may occur in the vicinity of equipment marked with the following symbol: [electromagnetic interference symbol].

NOTE1: At 80 MHz and 800 MHz, the higher frequency range applies.

NOTE2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

More information on EMC compliance of the device can be obtained from Rossmax website: www.rossmax.com.

Models: CF155F Blood Pressure Monitor, CF155F, Blood Pressure Monitor, Pressure Monitor, Monitor

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