Focusing on your health

State-of-the art technology is an integral part of modern healthcare. Accurate measurements are essential for  treating hypertension, one of the core risk factors of cardiovascular disease.


In the patient’s best interest

Reliability and safety are a top priority, particularly in intensive care. Our blood pressure modules have been used around the world for decades, and we continue advancing them under close observance of international standards.


Satisfied customers – our primary goal

The consideration and fulfillment of special customer wishes and requirements is a key element of our company policy.
Our technical service guarantees the quality and operability of your products.


PAR products in space – simply out of this world

Produkt Highlights


Ambulatory NIBP monitor that ascertain the blood pressure during the inflation of the cuff.

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NIBP 2020 UP

In-patient, non-invasive, automatic blood pressure module for monitors.

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Ambulatory NIBP monitor that acsertein the blood pressure during the deflation of the cuff.

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PAR Medizintechnik from Berlin – the experts in NIBP technology

Our highly qualified experts find innovative solutions that can be adapted to the individual requirements of today's medical technology. Our state-of-the art technologies and the use of hand-picked materials guarantee the high quality of analysers and blood pressure cuffs. We offer quality made in Germany.

Customer satisfaction is our top priority. Our Service Department is always available to answer your questions and solve your problems.


Certification and audit news

We are proud to inform our customers that our company is certified for ambulatory blood pressure monitors and blood pressure measurement modules according to Regulation (EU) 2017/745 on medical devices (in short: MDR) Annex IX. Likewise, the cuffs for blood pressure measurement meet the applicable requirements of the MDR.

In addition to our MDR certification audit 2022, we have also successfully completed the first MDR surveillance audit. Currently, the MDR conformity of our display software is being evaluated, which is currently still marketed under the Medical Device Directive 93/42/EEC (MDD for short).

In addition to the requirements of ISO 13485:2016, our quality management system fulfills the country-specific requirements of Canada and the USA according to the MDSAP audit program. During the last audit, the specific requirements of Australia were assessed. Our MDSAP certificate will soon be extended to include this country.


Medical engineering meets environmental protection

In addition, we are part of the Motzener Straße e.V. business network and support the "Green Power Plant" project. The project transparently shows to what extent the companies of the industrial area generate and use renewable energies as well as sustainably generated heat.