Sanitas SBM21 Инструкция по эксплуатации онлайн [20/52] 80602

Accessories Instruction for use, 4 x 1.5 V AA alkaline

batteries., storage pouch

Classification Internal supply, IPX0, no AP or APG,

continuous operation, type BF applied

part

Technical information is subject to change without notification

to allow for updates.

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This unit is in line with European Standard EN 60601-1-2 and

is subject to particular precautions with regard to electro-

magnetic compatibility (EMC). Please note that portable and

mobile HF communication systems may interfere with this

unit. More details can be requested from the stated Custo-

mer Service address or found at the end of the instructions

for use.

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This device is in line with the EU Medical Devices Directive

93/42/EC, the „Medizinproduktegesetz“ (German Medical

Devices Act) and the standards EN1060-1 (non-invasive

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 equipment – Part 2 – 30: Particular requirements

for the safety and essential performance of automated non-

invasive blood pressure monitors).

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The accuracy of this blood pressure monitor has been ca-

refully checked and developed 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.