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Uscom BP+

Device Name:BP Plus
Manufacturer:Uscom Ltd., Suite 2, Level 8, 66 -74 Clarence Street, Sydney, NSW 2000, AUSTRALIA.
Measuring functions:Blood pressure
Primary Client Use:Intended for professional use including central aortic pressure
Measurement Site:Upper Arm
Measurement Occurrence:Intermittent measurements at specified intervals or times
Availability:Available Currently
Assessment:

While the technology used in the Uscom BP+, to measure blood pressure, has been declared as being equivalent to that used in a clinically validated device, no evidence has been published to show that the devices have been compared according to a protocol compliant with (EU) 2017/745 and MEDDEV 2.7/1 rev 4.

Accuracy AssessmentRecommendationBasis
MedavalNoneAlthough equivalence to another device is claimed, this has not been tested to MDR requirements.
BIHS (UK and IRL)Professional useManufacturer declaration of equivalence

Device Family:Par Physio-PortB, PAR Tonoport VIB, Uscom BP+B (B BIHS Derivative)
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.

PAR Tonoport VI

Abou-Dakn M, Döhmen C, Wenzel S. Validation of the TONOPORT VI ambulatory blood pressure monitor in adults according to the European Society of Hypertension International Protocol revision 2010. J Hum Hypertens. 2017 Feb;31(2):89-92. Epub: 2016 Jul 14. doi: 10.1038/jhh.2016.40. PMID: 27411300.

ESH-IP:2010 - Pass General population (Note: Inflation method)

ESH-IP:2010 - Pass General population (Note: Deflation method)