Beurer BM 44
Device Model:
BM 44
Manufacturer:

OBL: Beurer GmbH, Söflinger Straße 218, 89077 Ulm, GERMANY.

OEM: Andon Health Co. Ltd., 3 Jinping Road, Ya'an Street, Nankai District, Tianjin 300190, CHINA.

Measuring functions:
Blood pressure
Primary Client Use:
Intended for self-measurement and home use
Measurement Site:
Upper Arm
Measurement Occurrence:
Single measurements only
Availability:
Available Currently
Availability according to Countries or Regions:
Germany, United Kingdom, Spain, France, Italy and Hungary
Device Manual:
Device Specifications:
Description:
The Beurer BM 44 is an automatic blood pressure monitor. Although its blood pressure measurement technology has been evaluated, it is not possible to base a determination on its accuracy from this research. Blood pressure measurements are taken from the upper arm. It is intended for self-measurement and home use.
Assessment:
The technology used in the Beurer BM 44, to measure blood pressure, has been assessed, in a general population, according to a non-standard protocol.
Recommendations:
Accuracy AssessmentRecommendationBasis
BP Medaval None When an evaluation is carried out using a non-standard protocol, no inference can be made on accuracy based on a standard protocol.
BP BIHS (UK and IRL) Self-measurement Published evidence
BP ESH (Europe) Self-measurement Published evidence
BP Stride BP Self-measurement for adults Published evidence
Device Family:
Validation Publications:

Lüders S, Krüger R, Zemmrich C, Forstner K, Sturm CD, Bramlage P. Validation of the Beurer BM 44 upper arm blood pressure monitor for home measurement, according to the European Society of Hypertension International Protocol 2002. Blood Press Monit. 2012 Dec;17(6):248-52. doi: 10.1097/MBP.0b013e32835b9e8e. PMID: 23147534.

ESH-IP:2002 General population (Note: ESH-02 not recognised since 01 July 2011)

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.

Andon KD-5031

Wu N, Zhang X, Wang W, Zhang H. Validation of the Andon KD5031 for clinical use and self-measurement according to the European Society of Hypertension International Protocol. Blood Press Monit. 2016 Oct;21(5):310-2. Epub: 2016 Jul 7. doi: 10.1097/MBP.0000000000000204. PMID: 27392206.

ESH-IP:2010 - Pass General population

Andon KD-5915

Huang QF, Wang J, Sheng CS, Zhang NN, Li Y, Wang JG. Validation of the ANDON KD-5915 blood pressure monitor for home blood pressure monitoring according to the European Society of Hypertension International Protocol. Blood Press Monit. 2010 Aug;15(4):232-4. PMID: 20658765.

ESH-IP:2002 - Pass General population

Andon KD-5917

Guo WG, Li BL, He Y, Xue YS, Wang HY, Zheng QS, Xiang DC. Validation of the Andon KD-5917 automatic upper arm blood pressure monitor, for clinic use and self-measurement, according to the European Society of Hypertension International Protocol revision 2010. Blood Press Monit. 2014 Aug;19(4):242-5. doi: 10.1097/MBP.0000000000000048. PMID: 24847724.

ESH-IP:2010 - Pass General population

Andon KD-595

Wu N, Zhang X, Wang W, Zhang H. Validation of the Andon KD-595 for clinical use and self-measurement according to the European Society of Hypertension International Protocol. Blood Press Monit. 2016 Apr;21(2):124-7. Epub: 2015 Nov. doi: 10.1097/MBP.0000000000000164. PMID: 26544523.

ESH-IP:2010 - Pass General population

Liu K, Wu D, Bing S, Li LY. Validation of the ANDON KD-595 automated upper-arm blood pressure monitor according to the universal standard. Blood Press Monit. 2024 Apr 1;29(2):103-106. Epub: 2023 Dec 14. doi: 10.1097/MBP.0000000000000686. PMID: 38193382.

81060-2:2019 - Pass General population

Andon KD-5965

Huang J, Li Z, Li G, Liu Z. Validation of the Andon KD-5965 upper-arm blood pressure monitor for home blood pressure monitoring according to the European Society of Hypertension International Protocol revision 2010. Blood Press Monit. 2015 Oct;20(5):283-5. Epub: 2015 May 5. doi: 10.1097/MBP.0000000000000129. PMID: 25968093.

ESH-IP:2010 - Pass General population

iHealth Track (KN-550BT)

Van Den Heuvel JFM, Lely AT, Franx A, Bekker MN. Validation of the iHealth Track and Omron HEM-9210T automated blood pressure devices for use in pregnancy. Pregnancy Hypertens. 2019 Jan;15:37-41. Epub: 2018 Nov 2. doi: 10.1016/j.preghy.2018.10.008. PMID: 30825925.

ESH-IP:2010 - Pass Pregnancy (n=33), Pre-eclampsia (n=10)

Shi L, Zhang XY, Sun JY, Chen JF, Ma YF, Zhou KY. Validation of the iHealth Track upper-arm blood pressure monitor KN-550BT in general population according to the AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018+AMD1:2020). Blood Press Monit. 2024 Feb 1;29(1):41-44. Epub: 2023 Sep 14. doi: 10.1097/MBP.0000000000000678 . PMID: 37702596.

81060-2:2020 - Pass General population