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Omron RS7 Intelli IT (HEM-6232T-E)
Device Name:
RS7 Intelli IT
Device Model:
HEM-6232T-E
Manufacturer:
Omron Corporation, Kyoto Head Office, Shiokoji Horikawa, Shimogyo ku, Kyoto 600-8530, JAPAN.
Measuring functions:
Blood pressure
Primary Client Use:
Intended for self-measurement and home use
Measurement Site:
Wrist
Measurement Occurrence:
Single measurements only
Availability:
Available Currently
Availability according to Countries or Regions:
Ireland
Description:
The Omron RS7 Intelli IT (HEM-6232T-E) is an automatic blood pressure monitor. Its blood pressure measurement technology has been proven to be accurate. Blood pressure measurements are taken from the wrist. It is intended for self-measurement and home use.
Assessment:
The technology used in the Omron RS7 Intelli IT (HEM-6232T-E), to measure blood pressure, has passed in two clinical validation studies, in a specific populations, according to recognised standard protocols, as published in peer-reviewed publications.
Recommendations:
Accuracy AssessmentRecommendationBasis
BP Medaval Recommended in certain condition(s) Validation in specific condition(s). See publications for details.
BP Stride BP Self-measurement for adults and obese adults Published evidence
Consumer BodyYear(s)LevelComment
BP Stiftung Warentest (DE) Latest: 2020 Good
Device Family:
Omron HEM-6232TP,Y, Omron RS7 Intelli IT (HEM-6232T-E)P, Omron HEM-6232T (HEM-6232T-AP)Y
Legend: P Stride Equivalence, Y Internal declaration
Validation Publications:

Tasic D, Topouchian J, Dragisic D, Tasic N, Hakobyan Z, Vatinyan S, Zelveian P, Asmar R. Reproducibility of the European Society of Hypertension - International Protocol for validation of blood pressure measuring devices in obese patients. J Hypertens. 2019 Sep;37(9):1832-1837. doi: 10.1097/HJH.0000000000002106. PMID: 31246893.

ESH-IP:2010 - Pass Arm circumference at least 32 cm or obesity (Note: Validation by Serbian team)

ESH-IP:2010 - Pass Arm circumference at least 32 cm or obesity (Note: Validation by Armenian team)

Karampela I, Dalamaga M, Stratigou T, Antonakos G, Nikolopoulos M, Tzortzis E, Diomidous M. Validation of an Automatic Wrist Blood Pressure Monitor in a Critical Care Setting. Stud Health Technol Inform. 2020 Jun 26;272:171-174. doi: 10.3233/SHTI200521. PMID: 32604628.

IA protocol Critically ill patients (Note: IA validation (n=45/45 - one pair in each of the patients))

Validation Publications for Equivalent Devices:

Note: This is a provisional list, as equivalence according to EU Regulation 2017/745 (e.g. MEDDEV 2.7/1 rev 4) is not proven. Accordingly, these publications are not used in the assessment of star-ratings.

Omron HEM-6232T

Saito K, Hishiki Y, Takahashi H. Validation of two automatic devices, Omron HEM-6232T and HEM-6181, for self-measurement of blood pressure at the wrist according to the ANSI/AAMI/ISO 81060-2:2013 protocol and the European Society of Hypertension International Protocol revision 2010. Vasc Health Risk Manag. 2019 Mar 6;15:47-55. doi: 10.2147/VHRM.S188089. PMID: 30881007. Available from: PMC6410757. eCollection 2019. Erratum in: Vasc Health Risk Manag. 2019 May 17;15:137.

81060-2:2013 - Pass General population

ESH-IP:2010 - Pass General population

The studies use the same data and are, therefore, not independent.

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