☰
🏠
📞  +353 1 6643768
 
📧  info@medaval.ie
      
PAR Tonoport VI
Device Name:
Tonoport VI
Manufacturer:
PAR Medizintechnik GmbH & Co. KG, Platinum, Sachsendamm 6, 10829 Berlin, GERMANY.
Measuring functions:
Blood pressure
Primary Client Use:
Intended for ambulatory blood pressure monitoring
Measurement Site:
Upper Arm
Measurement Occurrence:
Intermittent measurements at specified intervals or times
Availability:
Available Currently
Device Manual:
Click here to download the Device Manual
Device Specifications:
Click here to download the Device Specifications
Description:
The PAR Tonoport VI is an ambulatory blood pressure monitor. Its blood pressure measurement technology has been proven to be accurate, with a 2-star Medaval rating. Blood pressure measurements are taken from the upper arm. It is intended for ambulatory blood pressure monitoring.
Assessment:
The technology used in the PAR Tonoport VI, 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 ★★ Recommendation Recent clinical validation; recent protocol
BP BIHS (UK and IRL) ABPM Published evidence
BP ESH (Europe) ABPM Published evidence
BP Stride BP ABPM for adults (Preferred) Published evidence
Device Family:
PAR Tonoport VIB, Par Physio-PortB, Uscom BP+B
Legend: B BIHS Derivative
Validation Publications:

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)

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.

Uscom BP+

Glenning JP, Sheeran F, Cuthbert J, Harris W, Quinlan C, Mynard JP. Validation of the Uscom BP+ automated oscillometric blood pressure monitor for professional office use in children and adolescents according to the AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018). Hypertens Res.. Epub: 2024 Dec 24. doi: 10.1038/s41440-024-01992-1. PMID: 39719530.

81060-2:2019 - Pass General population (Note: Three standard cuffs: Extra Small (12 cm - 17 cm), Small Adult (16 cm - 24 cm) and Adult (22 cm - 32 cm))

81060-2:2019 - Fail General population (Note: Non-standard wide-range cuff (22 cm - 42 cm))

© Medaval Ltd. Please read the Terms and Conditions before using this site.