Sanitas SBM 30 Instructions For Use Manual page 18

• The instrument is in line with the EU Medical Products
Directive 93/42/EC, the German medical products act and
European standards EN1060-1 (non-invasive blood pres-
sure monitors, Part 1: general requirements) and EN1060-3
(non-invasive blood pressure monitors, Part 3: Supplemen-
tary Requirements for Electromechanical Blood Pressure
Measure ment Systems).
• If you are using the instrument for commercial or economic
purposes, you must check measurement precision regularly
in accordance with the "Operators' Ordinance on Medical
Products". Even in the case of private use, we recommend
checking measurement precision every two years at the
manufacturers.
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