Clinical Trial of YuWell YE660D Blood Pressure Monitor in General Population According to the ISO 81060-2:2018

Validation of the YuWell YE660D Oscillometric Upper-arm Blood Pressure Monitor for Clinic and Home in General Population According to the AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018)

The purpose of this study is to evaluate the accuracy of the YuWell YE660D oscillometric upper-arm blood pressure monitor for clinic and home in general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Universal Standard (ISO 81060-2:2018).

Inclusion Criteria:

• 12 Years and older;
• Subjects voluntarily participate in the clinical trial and sign the informed consent.

Exclusion Criteria:

• Disturbance of consciousness;
• Patients requiring hemodialysis;
• Taking anticoagulant drugs due to cardiovascular and cerebrovascular diseases;
• Pregnant and lactating women;
• Patients with cardiac arrhythmias;
• Other conditions that the investigator considers ineligible for clinical trial.