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12 Technical description
Main power supply
Main fuses (x2)
T 3,15 A L, 250 V
Electrical class
I
Type
A
Leak current
IEC 60601-1 compliant
Protection following a loss of power
Continuous audible alarm and patient vented to
atmosphere
Internal battery (Air Liquide ref. KY633300)
Type
NiMh
Rated voltage: 24 V
Rated capacity 2X4500 mAh
Battery capacity (new and charged battery) with
the standard ADULT configuration
3 h typical
Ambient temperature: 25°C
Charging time (h)
10 h typical (according to environmental condi-
tions)
Isolation
Separation from the power supply
To electrically separate the
Monnal T75
from the
power supply, disconnect the flexible power ca-
ble.
12.4.3.3 Electromagnetic Compatibility
All of the information set out below was obtained from the normative requirements to which the manu-
facturers of electro-medical devices are subject, within the meaning of standard IEC 60601-1-2 Ed4.
The medical device is compliant with the electromagnetic compatibility standards in force; neverthe-
less the user shall ensure that any electromagnetic interference does not create an additional risk,
such as radio-frequency transmitters or other electronic devices.
In this section you will find the information required to ensure that the installation and putting into op-
eration of your medical device is carried out under the best possible conditions in terms of electro-
magnetic compatibility. The various leads attached to the medical device must be separated from
each other.
Certain types of telecommunications mobile devices such as mobile phones may interfere with the
medical device. The recommended separation distances in this section must therefore be strictly ob-
served.
The medical device must not be used in close proximity to other equipment or placed on top of other
equipment. If this cannot be avoided, its operation under the conditions of use must be checked be-
forehand. The use of accessories other than those specified or sold by
Air Liquide Medical Systems
as
replacement parts may have the consequence of increasing the emissions or decreasing the immunity
of the medical device.
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