vivocare Guardy, Instruction Manual

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Technical information is subject to change without notification to allow for updates.
• This unit is in line with European Standard EN 60601-1-2 and is subject to particular
precautions with regard to electromagnetic compatibility (EMC). Please note that port -
able and mobile HF communication systems may interfere with this unit. More details
can be requested from the stated Customer Service address or found at the end of
the instructions for use.
• This device is in line with the EU Medical Devices Directive 93/42/EC, the “Medizin -
produktegesetz” (German Medical Devices Act) and the standards EN 1060-1 (non-in -
vasive sphygmomanometers, Part 1: General requirements), EN 1060-3 (non-invasive
sphygmomanometers, Part 3: Supplementary requirements for electro-mechanical
blood pressure measuring systems) and IEC 80601-2-30 (Medical electrical equip
-
ment – Part 2 – 30: Particular requirements for the safety and essential performance
of automated non-invasive blood pressure monitors).
• The accuracy of this blood pressure monitor has been carefully checked and de -
veloped with regard to a long useful life. If using the device for commercial medical
purposes, it must be regularly tested for accuracy by appropriate means. Precise
instructions for checking accuracy may be requested from the service address.