Kraujospūdžio matuoklis OMRON M6 Comfort (2024) su adapteriu

Trumpai apie prekę

Prekė: Kraujospūdžio matuoklis OMRON M6 Comfort (2024) su adapteriu. Kategorija: Kraujospūdžio matuokliai.

• Gamintojas: Omron
• Modelis: 7380-S

The OMRON M6 Comfort AFib is a next-generation digital blood pressure monitor. New TruRead pro objective results function (average of 3 measurements with adjustable interval) and new Intellisense AFib technology (detection of atrial fibrillation with each pressure measurement). Highly precise results thanks to the universal INTELLI cuff. The blood pressure monitor has a split pro memory of 2 users and a number of other functions (high pressure indicator, cuff insertion control, motion indicator, arrhythmia detection).

Product Description

• The device is designed to pro measure blood pressure on the arm.
• Very large, clear and easy to read 3-line display. With a dual display, you can compare the latest results with previous blood pressure values.
• Intellisense technology* – fast and accurate measurement.
• Universal INTELLI cuff (pro arm circumference 22-42 cm) – eliminates errors when placed incorrectly on the arm, because it has a larger measuring surface and thus ensures accurate measurement of blood pressure also at home. One pro cuff of normal and thicker arm (replaces two cuffs and eliminates wrong cuff selection).
• TruRead mode (new) – pro objective results; the device performs 3 consecutive measurements with the possibility of setting the interval between individual measurements (15/30/60/120 seconds) and displays the average value.
• Intellisense AFib technology (new) – the device automatically detects atrial fibrillation with each blood pressure measurement. This is not a diagnosis, but only the detection of possible atrial fibrillation. If there is a possibility of atrial fibrillation, the appropriate symbol will appear on the display and in this case you should contact your doctor and consult with him about your health condition. **
• Hypertension indicator (icon on the display) – displays if any of the measured values is higher than the recommended values of optimal blood pressure pro home measurements (135/85 mmHg).
• The device helps to detect the risk of morning hypertension – elevated blood pressure values in the morning are an independent factor of cardiovascular risk.
• Control of the correct insertion of the cuff (icon on the display) – warns about inadequate (insufficient) insertion of the cuff. If the OK symbol is displayed, the results are reliable.
• Assessment and display of arrhythmia (irregular pulse) – if this symbol appears too often, contact your doctor.
• Indicator warning of inadequate movement during measurement – movement during measurement may affect its accuracy. If you move during the measurement, a movement symbol will appear. The measurement must be repeated.
• Prevention of stroke – hypertension and atrial fibrillation are the 2 main risk factors for stroke. OMRON blood pressure monitors accurately measure blood pressure and detect arrhythmias.
• Split memory pro 2 users (2x100 memory with date and time) + HOST mode (after selecting the HOST mode, no measured value will be saved in the device memory).
• Calculation of the average blood pressure from the last 2 or 3 measurements taken in 10 minutes.
• Weekly morning and evening averages with measured values.
• Clinically approved – such marked devices are recommended by the Czech Society for Hypertension (ČSH) and meet international standards for clinical validation.
• Also tested in pregnant women and diabetics.
• The kit also includes the original Omron power supply.

Technical data:

• Measurement range:
• Blood pressure SYS: 60 – 260 mmHg, DIA: 40 – 215 mmHg.
• Pulse: 40 – 180 strokes/min.
• Measurement accuracy: Blood pressure: ± 3 mmHg, Pulse: ± 5 % of the measured value.
• The new alkaline batteries last for about 700 measurements (the number of measurements may decrease if you use TruRead mode).
• Weight of the main unit approx. 440 g without batteries, cuff weight approx. 163 g.
• External dimensions (S x W x G): 191 mm x 85 mm x 117 mm.
• CE 0197.
• Classification according to the European directive pro medical devices MDR 2017/745 – class II A.

Specifications