Maico MA 1, Руководство по эксплуатации

Страница: 8 / 22

MA 1 Operating Manual
4
8100216-3 (D-0100192)
3.1. Important Safety Note
The MA 1 should always be operated in a quiet room with minimal magnetic influence,
to ensure that examinations are not disturbed by external noise.
Electro-medical instruments that emit strong electromagnetic fields (e.g. microwaves,
radiotherapy devices) can affect the operation of the MA 1
Therefore, the operation of these instruments in close proximity to the MA 1 should be
avoided at all times.
The examination room should have a normal temperature between 15˚C/ 59˚F and
35˚C/ 95˚F. If the instrument has cooled down during transportation, please wait for it
to warm up to room temperature before operation.
Attention
PLEASE READ THE ENTIRE MANUAL CAREFULLY BEFORE OPERATING THIS
INSTRUMENT.
Please only use this instrument as described in the manual.
Please familiarize yourself with the instrument and its operation before using.
Should defects or damages be suspected, please do not, under any circumstances, use
or attempt to fix the instrument yourself.
Calibration of the instrument: The audiometer and the headphone complement each
other and share the same serial number (i.e. 63252). Therefore, the instrument shall
not be used with any other headphone prior to recalibration. Recalibration also needs
to be conducted, when a defective headphone is replaced.
NOTE: Uncalibrated instruments may lead to faulty measurements.
Take note to ensure that all the accessories have been properly connected.
To avoid person-to-person cross contamination of communicable diseases, parts that
come in direct contact with the patient (i.e. earphone cushions) should be
disinfected using commercial disinfectant after each use.
In accordance with the Electronic Equipment Act for disposal of electronic
equipment, the customer is obliged to dispose of the used consumables,
according to appropriate regulation at own cost.
This equipment is intended to be connected to other equipment thus forming a
Medical Electrical System. External equipment intended for connection to signal input,
signal output or other connectors shall comply with the relevant product standard e.g.
IEC 60950-1 for IT equipment and the IEC 60601-series for medical electrical
equipment. In addition, all such combinations – Medical Electrical Systems – shall
comply with the safety requirements stated the general standard IEC 60601-1, edition