Beurer BM 53 vs Omron M6 Comfort

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BM 53 compared with M6 Comfort

	BeurerBM 53	OmronM6 Comfort
Overview
Released
Released	–	–
Measuring
Type
Type	Upper arm	Upper arm
Clinically validated
Clinically validated	–	Yes
Irregular heartbeat detection
Irregular heartbeat detection	Yes	Yes
AFib detection or ECG
AFib detection or ECG	Yes	Yes
Method
Method	Automatic oscillometric upper-arm measurement during deflation; first on-sale date not established	Automatic oscillometric upper-arm measurement; HEM-7360-E, distinct from M6 Comfort AFib HEM-7380-E and earlier M6 Comfort revisions. First on-sale date not established
Accuracy
Accuracy	Maker manual specifies display accuracy of ±3 mmHg for systolic and diastolic pressure and ±5% of the displayed pulse value; this specification is distinct from clinical validation	Maker's pressure accuracy ±3 mmHg and pulse accuracy ±5% of displayed reading; systolic range 60–260 mmHg, diastolic 40–215 mmHg and pulse 40–180 beats/minute
Clinical validation
Clinical validation	Beurer states clinical testing to ISO 81060-2 and suitability during pregnancy; exact independent registry confirmation was not established	Maker manual states an 85-subject investigation under EN ISO 81060-2:2014 and compliance with 2019+A1:2020, plus pregnancy/preeclampsia and type II diabetes validation. Medaval attributes BIHS/STRIDE recommendations to BP760N HEM-7320-Z equivalence, but notes that the unpublished assessment cannot be verified against MDR requirements; blood-pressure validation does not establish diagnostic accuracy of rhythm indicators
Features
Features	Advanced arrhythmia indication including possible atrial fibrillation, automatic triple measurement, resting indicator, cuff fit check, classification scale and automatic switch-off	Selectable AFib mode takes three consecutive measurements at 30-second intervals and displays their average with a possible-AFib indicator. This is pulse-wave screening, not ECG recording or diagnosis; unlike the newer HEM-7380-E, screening is not automatic in every single reading. Exact manual and maker headline confirm the mode despite the web table's AFib No entry. Cuff-wrap, movement, irregular-heartbeat and high-pressure indicators
Cuff
Cuff fits
Cuff fits	22–42 cm	22–42 cm
Cuff
Cuff	Supplied upper-arm cuff	Included HEM-FL31 Intelli Wrap cuff, 22–42 cm arm circumference; approximately 145 × 532 mm, 750 mm tube and 163 g
Connections and memory
Users
Users	2	2
Readings stored
Readings stored	100 per user	100 per user
Bluetooth and app
Bluetooth and app	No	No
Memory
Memory	100 readings per user; average of all saved readings and morning/evening readings from the last seven days	Up to 100 readings per user for two users; unsaved single-reading guest mode does not offer AFib screening. Latest two/three-reading average within ten minutes and morning/evening weekly averages; dual display compares current and earlier results
App
App	Scan & Save in beurer HealthManager Pro uses a smartphone camera to record the display; no Bluetooth connection	No Bluetooth or OMRON connect transfer
Power
Power	Four 1.5 V AAA batteries or optional DC 5 V, 1 A mains adaptor; maker claims approximately 300 measurements depending on pressure	Four AA batteries included, DC 6 V / 4 W; optional AC adapter sold separately. Approximately 1000 measurements using new alkaline batteries; AFib mode consumes three regular measurements per indication
Design
Display details
Display details	Illuminated LCD, 8.0 × 7.4 cm, with black digits on a white background	Digital LCD with side-by-side readings; monitor IP20. Optional adapter IP21/IP22 classifications do not apply to the monitor
Size
Size	14.00 × 9.40 × 4.60 cm (L × W × H), current maker product page	Approximately 191 × 85 × 120 mm (W × H × L); 460 g without batteries
In the box
In the box	Monitor, 22–42 cm cuff, four AAA batteries and storage bag; maker product page also lists a blood pressure record	Monitor, HEM-FL31 cuff, four AA batteries, storage case and instruction manuals 1/2