The digital Erkameter E product family - for blood pressure readings without any doubt

MEASUREMENT METHOD

Medically accurate blood pressure measurements according to latest recommendations of the European Society of Hypertension (ESH): with its combined measuring modes Automatic and Manual all digital Erkameter E strictly implement the standards of ESH and guarantees any time dependable and medically relevant

measuring values in the professional diagnostics. Even by measuring difficult patients groups – for example pregnant – the CLASSIC modes provides correct values: The measurement is taken by auscultation with the stethoscope, reliable thanks to your expert’s assessment.

MEASUREMENT ACCURACY

Validated by an independent test lab using the standards of the European Society of Hypertension all digital Erkameter E achieve best grades concerning measuring exactness in comparison to all other topically tested blood pressure measuring instruments. Small divergence, big effect: a systematic measuring mistake

from -/+ 5mmHG overlooks the need of treatment of leads to the unwarranted treatment of significant patient’s groups. The measuring exactness of each digital Erkameter E creates trust in the measuring values and therefore in diagnosis and therapy.

HYGIENE

ERKA offers a comprehensive assortment of recyclable disposable cuffs – the use of these cuffs still is the safest protection against infections for patient and doctor. However, due to their unique surface and materiality all ERKA Green Cuff blood pressure cuffs can be disinfected thoroughly and fast. The special skin compatibility was verified in dermatological test several times and provides security and wearing comfort for the patient. Every single ERKA Green Cuff blood pressure cuff carries the predicate BIOCOMPATIBLY – the logical renunciation of PVC and DEHP in our products connects ecology and efficiency in optimum way.

IT-INTEGRATION

Designed for integration into your existing practice or clinic software, all digital Erkameter E meet the technical requirements for unhindered data exchange between the device and the electronic patient record.