Montex
Prolife PX7 Premium
Preferred devices rules
Preferred devices are upper-arm cuff devices with at least one STRIDE BP approved validation study, which was published within the last 10 years and used a recent protocol (AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018); ANSI/AAMI/ISO 2013 or 2009; ESH-IP 2010). Preferred devices for home use also have automated storage of multiple readings, or mobile phone, PC or internet link connectivity enabling data transfer.
Market Availability
Available
Population
Adults
Use
Home
Measurement Site
Upper arm cuff
Measurement Method
Automated oscillometric
Validated Cuff Sizes (cm)
22-45
Additional Features
Atrial fibrillation detection, Automated storage of multiple readings, Wide-range cuff
Validation studies according to established protocols
Population
Adults
Protocol and version (year)
AAMI_ESH_ISO Universal Standard (ISO 81060-2:2018) 2018
Year of validation study publication
2025
Link