Sperian Titmus V2 User Manual

Titmus V4 / Titmus V2
Electromagnetic Environment - Guidance
This section applies to the following models — Titmus V4, Titmus V2.
Medical Electrical Equipment needs special precautions regarding Electromagnetic Emissions and Immunity and needs to
be installed and put into service according to the Electromagnetic Emissions and Immunity information provided in this
document.
Portable and mobile RF communications equipment can affect Medical Electrical Equipment.
Equipment should not be used adjacent to or stacked with other equipment and, if adjacent or stacked use is necessary,
the Equipment should be observed to verify normal operation in the configuration in which it will be used.
Guidance and Manufacturer’s Declaration - Electromagnetic Emissions
The Titmus V4/V2 is intended for the use in the electromagnetic environment specified below. The customer or the user of
the Titmus V4/V2 should ensure that it is used in such an environment.
Use of cables, other than those specified in this manual, may result in increased Emissions or decreased Immunity of the
Titmus V4/V2.
Emissions Test Compliance Electromagnetic environment -guidance
RF emissions
CISPR 11
Group 1 The Titmus V4/V2 uses RF energy only for its internal
function. Therefore, its RF emissions are very low and
are not likely to cause any interference in nearby
electronic equipment.
RF emissions
CISPR 11
Class A
Harmonic Emissions
IEC 61000-3-2
Class A
Voltage fluctuations / flicker emissions
IEC 61000-3-3
Complies
The Titmus V4/V2 is suitable for use in all establishments
other than domestic and those directly connected to the
public low-voltage power supply network that supplies
buildings used for domestic purposes.
Guidance & Manufacturer’s Declaration - Electromagnetic Immunity
The Titmus V4/V2 is intended for the use in the electromagnetic environment specified below. The customer/user of the
Titmus V4/V2 should ensure that it is used in such an environment.
Immunity Test IEC 60601 test
level
Compliance level Electromagnetic environment - guidance
Electrostatic discharge
(ESD)
IEC 61000-4-2
± 6 kV contact
± 8 kV air
± 6 kV contact
± 8 kV air
Floors should be wood, concrete or ceramic tile.
If floors are covered with synthetic material, the
relative humidity should be at least 30%.
Electrical fast
transient/burst
IEC 61000-4-4
± 2 kV for power
supply lines
± 1 kV for
input/output lines
± 2 kV for power
supply lines
± 1 kV for
input/output lines
Main power quality should be that of a typical
commercial or hospital environment.
Surge
IEC 61000-4-5
± 1 kV line(s) to
line(s)
± 2 kV line(s) to
earth
± 1 kV line(s) to
line(s)
± 2 kV line(s) to
earth
Main power quality should be that of a typical
commercial or hospital environment.
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines
IEC 61000-4-11
<5% U
T
(>95% dip in U
T
)
for 0,5 cycle
40% U
T
(60% dip in U
T
)
for 5 cycles
<5% U
T
(>95% dip in U
T
)
for 0,5 cycle
40% U
T
(60% dip in U
T
)
for 5 cycles
Main power quality should be that of a typical
commercial or hospital environment. If the user
of the Titmus V4/V2 requires continued
operation during power main interruptions, it is
recommended that the Titmus V4/V2 be powered
from an uninterruptible power supply or a
battery.
Page 21

Sperian Titmus V2 Specifications

General

Brand	Sperian
Model	Titmus V2
Category	Medical Equipment
Language	English