Home /  Omron HEM-907 (HEM-907-E7)

Omron HEM-907 (HEM-907-E7)

Device Name:HEM-907
Device Model:HEM-907-E7
Manufacturer:Sole: Omron Corporation, Kyoto Head Office, Shiokoji Horikawa, Shimogyo ku, Kyoto 600-8530, JAPAN.
Measuring functions:Blood pressure
Primary Client Use:Intended for professional use
Measurement Site:Upper Arm
Measurement Occurrence:Single measurements only
Availability:Available Currently

The technology used in the Omron HEM-907 (HEM-907-E7), to measure blood pressure, has passed in clinical validation studies, between general and pregnancy populations, according to recognised standard protocols, as published in peer-reviewed publications.

Accuracy AssessmentRecommendationBasis
Medaval RecommendationOlder clinical validation; older protocol; multiple clinical validations
BIHS (UK and IRL)Self-measurement for adults and the elderlyPublished evidence
ESH (Europe)Professional usePublished evidence
Japanese Society of HypertensionProfessional use (2016-2018)Published evidence
Stride BPProfessional use for adults and the elderlyPublished evidence

Validation Publications

White WB, Anwar YA. Evaluation of the overall efficacy of the Omron office digital blood pressure HEM-907 monitor in adults. Blood Press Monit. 2001 Apr;6(2):107-10. PMID: 11433132.

SP10:1996 - Pass General population

El Assaad MA, Topouchian JA, Darné BM, Asmar RG. Validation of the Omron HEM-907 device for blood pressure measurement. Blood Press Monit. 2002 Aug;7(4):237-41. PMID: 12198340.

ESH-IP:2002 - Pass General population

Omboni S, Riva I, Giglio A, Caldara G, Groppelli A, Parati G. Validation of the Omron M5-I, R5-I and HEM-907 automated blood pressure monitors in elderly individuals according to the International Protocol of the European Society of Hypertension. Blood Press Monit. 2007 Aug;12(4):233-42. PMID: 17625396.

ESH-IP:2002 - Pass General population

Gurpreet K, Tee GH, Karuthan C. Evaluation of the accuracy of the Omron HEM-907 blood pressure device. Med J Malaysia. 2008 Aug;63(3):239-43. PMID: 19248698.

Ad Hoc protocol General population (Note: Modified BHS/AAMI protocols)

Czarkowski M, Staszków M, Kostyra K, Shebani Z, Niemczyk S, Matuszkiewicz-Rowińska J. Determining the accuracy of blood pressure measurement by the Omron HEM-907 before and after hemodialysis. Blood Press Monit. 2009 Oct;14(5):232-8. PMID: 19938337.

ESH-IP:2002 - Fail Before haemodialysis

ESH-IP:2002 - Fail After haemodialysis

Davis GK, Roberts LM, Mangos GJ, Brown MA. Comparisons of auscultatory hybrid and automated sphygmomanometers with mercury sphygmomanometry in hypertensive and normotensive pregnant women: parallel validation studies. J Hypertens. 2015 Mar;33(3):499-505; discussion 505-6. doi: 10.1097/HJH.0000000000000420. PMID: 25380148.

BHS:1993 - Pass (A/A) Normotensive (n=170) and hypertensive (n=170) pregnancy

Relevant Publications

Halfon M, Wuerzner G, Marques-Vidal P, Taffe P, Vaucher J, Waeber B, Liaudet L, Ltaief Z, Popov M, Waeber G. Use of oscillometric devices in atrial fibrillation: a comparison of three devices and invasive blood pressure measurement. Blood Press. 2018 Feb;27(1):48-55. Epub: 2017 Sep 28. doi: 10.1080/08037051.2017.1383852. PMID: 28958152.

Measurements from the Omron HEM-907 (HEM-907-E7) are compared to those from the Microlife WatchBP Home (BP 3MX1-1) and the Omron R7 (HEM-637-IT) in atrial fibrillation, though not in a formal validation.