Omron R3-I Plus (HEM-6022-E)
Device Name:
R3-I Plus
Device Model:
HEM-6022-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:
Discontinued but still available
Device Manual:
Click here to download the Device Manual
Description:
The Omron R3-I Plus (HEM-6022-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. This device has been discontinued by the manufacturer but may be available through certain outlets.
Assessment:
The technology used in the Omron R3-I Plus (HEM-6022-E), to measure blood pressure, has passed in a clinical validation study, in a general population, according to a recognised standard protocol, as published in a peer-reviewed publication.
Recommendations:
Accuracy AssessmentRecommendationBasis
BP Medaval Legacy approval Older clinical validation; older protocol
BP BIHS (UK and IRL) Previous recommendation, now archived (Archived) Published evidence
BP Stride BP Self-measurement for adults (Unavailable) Published evidence
Device Family:
Omron R3 (HEM-6021-E)D, Omron R3-I Plus (HEM-6022-E)D,J, Omron HEM-6022J
Legend: D DET Equivalence, J JHS Implied Equivalence
Validation Publications:

Asmar R, Khabouth J, Topouchian J, El Feghali R, Mattar J. Validation of three automatic devices for self-measurement of blood pressure according to the International Protocol: The Omron M3 Intellisense (HEM-7051-E), the Omron M2 Compact (HEM 7102-E), and the Omron R3-I Plus (HEM 6022-E). Blood Press Monit. 2010 Feb;15(1):49-54. doi: 10.1097/MBP.0b013e3283354b11. PMID: 20032779.

ESH-IP:2002 - Pass General population

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 R3 (HEM-6021-E)

Eckert S, Gleichmann U, Zagorski O, Klapp A. Validation of the OMRON R3 blood pressure self-measuring device through simultaneous comparative invasive measurements according to protocol 58130 of the German Institute for Validation. Blood Press Monit. 1997 Aug;2(4):189-192. PMID: 10234115.

58130:1995 - Pass General population (Note: (n=75/15))

Dieterle T, Battegay E, Bucheli B, Martina B. Accuracy and 'range of uncertainty' of oscillometric blood pressure monitors around the upper arm and the wrist. Blood Press Monit. 1998;3(6):339-46. PMID: 10212375.

BHS:1993 - Fail General population (Note: No grades in abstract)

SP10:1992 - Fail General population

Watson S, Wenzel RR, di Matteo C, Meier B, Lüscher TF. Accuracy of a new wrist cuff oscillometric blood pressure device: comparisons with intraarterial and mercury manometer measurements. Am J Hypertens. 1998 Dec;11(12):1469-74. PMID: 9880129.

IA protocol - Pass General population (Note: (n=100))

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