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Storz D-ACTOR 200 - Safety during treatment of the patient; Warning against damage to equipment and the device

Storz D-ACTOR 200
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19 620 02 0117
7
General Safety Information
Disconnect the D-ACTOR
®
200 from the mains before starting any cleaning or
maintenance work!
Disconnect the connected handpieces from the device before carrying out cleaning
and maintenance work. Do not reconnect them until they have been completely
reassembled!
The optional KARL STORZ foot switch must not be used in potentially explosive
atmospheresaccordingtoclassicationAPasperIEC60601.
Protection against noise
The noise level during administration of pulses is within the safe area. Nevertheless,
we recommend wearing suitable ear protection during treatment in order to minimise
exposure to noise.
1.1.2 Safety during treatment of the patient
General note:
Organs with gas inclusions, in particular parts of the lung, are NOT allowed to be
exposed to pulses.
As it passes through tissue, the pulse energy is slightly reduced; this reduction is
signicantlyweakenedbythebonestructure.
Pulses can give rise to undesirable heart reactions. The patient must be continuously
observed during the treatment.
Only perform treatments approved by STORZ MEDICAL AG!
The user is responsible for correctly positioning the handpieces and correctly selecting
the treatment zone.
No more than 6,000 pulses are allowed to be administered without interruption.
Treatment with the suction cup must be limited to 30 minutes.
1.2 Warning against damage to equipment and
the device
Any damage to the device resulting from incorrect operation is not covered by the
manufacturer’s warranty.
Electromagnetic compatibility
This device complies with the requirements of the applicable standard on
electromagnetic compatibility.
Nevertheless, portable and mobile HF communications equipment (e.g. mobile
phones) can interfere with medical electrical equipment.
This device is subjected to special precautions regarding EMC and needs to
be installed according the EMC guidelines in Chapter 7.4.1 eMC guidelines and
ManufaCturers deClaratiOn.

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