Warnings, Cautions, and Errors
The GSI Pello Audiometer is designed to be used with a hospital grade outlet.
Injury to personnel or damage to equipment can result when a three-prong to
two-prong adaptor is connected between the GSI Pello power plug and an AC
outlet or extension cord.
Warning!
To avoid the risk of electric shock, this equipment must only be connected to
supply mains with protective earth.
Do not block access to the power switch. Do not position the GSI Pello ME
EQUIPMENT so that it is difficult to operate the disconnection device.
Audiometers should be interconnected with accessories that have the proper
electrical compatibility Connection of accessories not meeting these electrical
compatibility requirements may result in electrical leakage currents in excess
of those allowed by the standard and present a potential electrical shock hazard
to the person being tested.
When testing with the High Frequency earphones, do not allow the
presentation of the signal at the maximum dB HL to exceed 10 minutes. The
buildup of increased temperature can cause harm to the earphones. This caution
label refers the user to the accompanying literature and manuals.
This icon indicates that the GSI Pello is in compliance with applied part Type B
requirements of IEC 60601-1.
The GSI Pello is designed for compliance to IEC and ES 60601-1 when used in
the patient vicinity.
In the presence of high intensities, a yellow light will appear per channel as a
warning indictor (IEC 60645-1 and ANSI S3.6).
Any program aimed at obtaining reliable records of hearing thresholds should be
staffed and supervised by appropriately trained individuals.
Latex is not used anywhere in the manufacturing process. The base material for
the earphone cushions is made from natural and synthetic rubber.
Warning!
No modifications of the equipment are allowed by anyone other than a qualified
GSI representative.
In this manual the following two labels identify potentially dangerous or
destructive conditions and procedures.
The WARNING label identifies conditions or practices that may present danger
to the patient and/or user.
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