Cardioline ar1200view, Руководство пользователя

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8
the message “
? Press 1
”:
Q
1
to obtain the printout) sums up the
operations linked to the single commands presented in the manual.
Further information and clarifications can be requested directly from:
CARDIOLINE ® - Supporto Prodotto
Strada Rivoltana Nuova, 53, I - 20060 Vignate (MI) ITALIA
e-mail: et.service@etmed.biz
tel. +39 02 95 05 181 fax: +39 02 95 66 013
1.2 Information and recommendations relating to
safe use
-
The electrical system used by the device must be in accordance with the
standard in force.
-
Always use the equipment according to the instructions in this manual.
-
The device is equipped with a set of standard accessories. For reasons
of safety, reliability and conformity with the Medical Devices Directive
93/42/EEC, use only original accessories or accessories approved by the
manufacturer.
-
The device is equipped with a special long-life thermal head writing
system, which allows maximum writing precision. To avoid frequent and
costly replacements and repairs, always use the original paper or paper
approved by the manufacturer. The manufacturer will not accept liability
for any damage to the device or any other adverse effect caused by the
use of unsuitable paper.
-
Do not subject the device to impact or excessive vibrations.
-
Do not allow liquids to penetrate inside the device. If this should
accidentally occur, have the device tested by an Authorised Assistance
Centre to verify its functional efficiency, before using it again.
-
Make sure that the value of the supply voltage corresponds to that
indicated on the data plate of the device.
-
If you are using the device in connection with others, ensure that: all
connections are made by skilled persons; all connections comply with
safety regulations; all other devices connected respond likewise to
regulations. Non-compliance with regulations can cause physical harm to
the patient connected and to the person operating the device. Should it
be difficult to obtain the necessary information for assessing the risk of
the individual connections, apply directly to the manufacturers
concerned or avoid making the connections.
-
In the event of other equipment being connected directly or indirectly to
the patient, check for the possible risks caused by the sum of the
leakage currents on the body of the patient.
-
The device is protected against defibrillation discharges in accordance
with IEC standard 601-1-25; to ensure that the signal is restored, use