X3 Comfort AFib
5 years of warranty *
Upper arm blood pressure monitor with early AFib detection
The OMRON X3 Comfort AFib is a clinically validated upper arm blood pressure monitor designed to simplify home hypertension tracking. It features Atrial fibrillation (AFib) detection, a 3× measurement function with automatic averaging, an Intelli Wrap Cuff (22–42 cm) and Intellisense technology for comfortable, controlled inflation. Supports two users with 60 readings each.
Specifications
- Weight of Device (kg)
- Weight of Device (kg)
- 0.34
- Cuff Type
- Cuff Type
- Intelli Wrap Cuff 22–42 cm
- Cuff Wrap Guide
- Cuff Wrap Guide
- Yes
- Memory
- Memory
- 2 users x 60 readings
- Irregular Heartbeat Detection
- Irregular Heartbeat Detection
- Yes
- Body Movement Detection
- Body Movement Detection
- Yes
- Validation
- Validation
- Clinical Validation, Diabetic Validation, Pregnancy Validation
- AFib detection
- AFib detection
- No
- Easy High Blood Pressure Indicator
- Easy High Blood Pressure Indicator
- No
- Advanced Positioning Sensor
- Advanced Positioning Sensor
- No
- Intellisense
- Intellisense
- Yes
- Storage Case Included
- Storage Case Included
- Yes
- Averaging Function
- Averaging Function
- No
- Connected
- Connected
- No
- Item Dimensions (mm)
- 105 x 152 x 85
What's in the box?
X3 Comfort, Intelli Wrap arm cuff, 4 x AA batteries, storage case, instruction manual.
* For home blood pressure monitors in Europe, Cerner Enviza, survey with cardiologists (2023)
Bilo G, Sala O, Perego C, et al. Impact of cuff positioning on blood pressure measurement accuracy: may a specially designed cuff make a difference?. Hypertens Res. 2017;40(6):573–580. Beschikbaar op https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5506235/
Topouchian J. et al. Clinical accuracy of the Omron M3 Comfort® and the Omron Evolv® for self-blood pressure measurements in pregnancy and pre-eclampsia - validation according to the Universal Standard Protocol. Vasc Health Risk Manag. 2018 Aug 31;14:189-197. Beschikbaar op https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124447
Chahine M. et al. Validation of BP devices QardioArm® in the general population and Omron M6 Comfort® in type II diabetic patients according to the European Society of Hypertension International Protocol (ESH-IP). Med Devices (Auckl). 2017 Dec 27;11:11-20. Beschikbaar op https://www.ncbi.nlm.nih.gov/pubmed/29343992