A study to collect data recorded by devices for cNIBP evaluation purposes.
The study is going to be conducted to collect data from the devices used in the study for future AMS engineering purposes as deemed appropriate by the Sponsor.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
12
To measure blood pressure in different circumstances with noninvasive blood pressure device
Data collection of NIBP measurement
To collect data recorded by devices for cNIBP evaluation purposes.
Time frame: through study completion, average of one day
Collect number of adverse events (AEs), serious adverse events (SAEs), and device issues
The safety objective is to collect safety information, including type and number of adverse events (AE), serious adverse events (SAE), and device issues.
Time frame: through study completion, an average of one day
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