Clinical Trial of Wrist Blood Pressure Monitor in Conformance With the EN ISO 81060-2:2019/A1:2020 Standard

Inclusion Criteria: 1. Subjects should voluntarily participate in the clinical trial and sign the informed consent form. 2. Subjects must be willing and able to follow the investigation procedures. 3. Subjects are over 18 years old whose wrist circumference should be within 13.0-20.0 cm. Exclusion Criteria: 1. Subjects with serious arrhythmias (atrial fibrillation, atrial flutter, ventricular flutter, ventricular fibrillation, ventricular tachycardia, borderline tachycardia, sinus arrest, pathological sinus syndrome, pacemaker rhythm) showed by electrocardiogram during screening period. 2. Subject with prior allergy to nylon, fluororubber, thermoplastic polyurethane elastomer (TPU), or polyvinyl chloride (PVC) materials. 3. Subjects with prior arterial obstructive disease or arteritis. 4. Subjects who had previously undergone mastectomy. 5. Subjects with wound or wrist inflammation were measured. 6. Subjects who are receiving intravenous infusion, blood transfusion, or other catheters at the site of measurement. 7. Subjects who had eaten, drank, smoked or exercised vigorously in the 30 minutes prior to the study. 8. Subjects who have participated in other clinical trials within 30 days that may affect this trial. 9. Subjects who the investigator consider inappropriate to attend the trial.