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Prolife PA3 Backlight - Information Provided by Manufacturer

Prolife PA3 Backlight
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21
EN
16 INFORMATION PROVIDED BY
MANUFACTURER
The Digital Blood Pressure Monitor Prolife PS1 is intended for use in the electro-
magnetic environment specified below. The customer or the user of the Prolife
PS1 should assure that it is used in such an environment.
Electromagnetic emissions: (IEC 60601-1-2)
Emission Test Compliance Electromagnetic environment
RF emission CISPR 11 Group 1
The Prolife PS1 uses RF en-
ergy only for internal functions.
Therefore, this RF emission is ex-
tremely weak and there is little
chance of it creating any kind of
interference whatsoever with
nearby electronic equipment
RF emissions CISPR 11 Class B The Prolife PS1 is suitable for
use in all establishments, includ-
ing domestic establishments
and those directly connected to
the public low voltage power
supply network that supplies
buildings used for domestic
purposes
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage fluctuations/
flicker IEC 61000-3-3
Not applicable
Electromagnetic immunity: (IEC 60601-1-2)
Immunity test
IEC 60601-1-2
test level
Compliance
level
Electromagnetic environ-
ment – guidance
Electrostatic dis-
charge (ESD) IEC
61000-4-2
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
Floors should be wood, con-
crete or ceramic tile. If floors
are covered with synthetic
material, the relative humid-
ity should be at least 30 %
Electric fast tran-
sient/burst IEC
61000-4-4
±2 kV for power
supply lines
±1 kV for input/
output lines
Not applicable Mains power quality should
be that of a typical commer-
cial or hospital environment
Surge
IEC 61000-4-5
±1 kV differential
mode
±2 kV common
mode
Not applicable

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