Overview
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).
Eligibility
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.
