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D-0126050 rev 1 - 270+ Operating Manual
2. UNPACKING AND INSTALLATION
2.1. GENERAL
Please check the contents of the shipping carton against the delivery note to make sure that all items ordered
have been included. If anything is missing, please contact the distributor who supplied the audiometer or
Amplivox if purchased directly.
Please retain the carton and packaging as the instrument will need calibrating on an annual basis and should
be returned to Amplivox in its original shipping carton.
For supply in US only: Federal Law restricts this device to sale by or on the order of a licensed medical
professional.
2.2. MARKINGS
The following markings can be found:
Refer to instruction manual.
Definition: Type B applied part – an applied part providing protection against electric
shock, particularly regarding allowable patient leakage current and patient auxiliary
current.
The applied parts are the left & right earphones, bone vibrator, insert masker, patient
response switch and the associated cables.
WEEE (EU-directive)
This symbol indicates that when the end-user wishes to discard this product, it must be
sent to appropriate collection facilities for recovery and recycling. Failing to do so may
endanger the environment.
The CE-mark indicates that Amplivox Ltd meets the requirements of Annex II of the
Medical Device Directive 93/42/EEC. TÜV Product Service, Identification No. 0123,
has approved the quality system.
The output from the mains AC adapter is Direct Current.
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