Validation Study of CONTEC08C Electronic Sphygmomanometer

Validation of the CONTEC08C Oscillometric Blood Pressure Monitor in General Population According to the AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018)

The purpose of this study is to assess the accuracy of the CONTEC08C automated oscillometric upper-arm sphygmomanometer in the general population for clinical use 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:

• Subjects aged 12 to 79 years
• Subjects voluntarily participate in the clinical trial and sign the informed consent.

Exclusion Criteria:

• Subjects with cardiac arrhythmias;
• Pregnancy;
• Poor quality Korotkoff sounds;
• Subject with an arm injury incompatible with the use of a cuff-based sphygmomanometer;
• Other conditions that the investigator considers ineligible for clinical trial.