AmpliVox Otowave 302+, Инструкция по эксплуатации

Страница: 9 / 65

UNPACKING AND INSTALLATION
8 OTOWAVE 302+ INSTRUCTION FOR USE
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 tympanometer 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:
Symbol Explanation
Type B applied parts. According to IEC 60601-1.
Patient applied parts that are not conductive and can be immediately released from the
patient.
Refer to instruction manual.
WEEE (EU-directive)
This symbol indicates that when the end-user wishes to discard this product, it must be sent to
separate collection facilities for recovery and recycling. Failing to do so may endanger the
environment.
0123
The CE-mark indicates that Amplivox Ltd. meets the requirements of Annex II of the Medical
Device Regulation 2017/745. TÜV Product Service, Identification No. 0123, has approved the
quality system.
Serial number.
Date of manufacture.
The output from the mains AC adapter is Direct Current.
Do not re-use.
Ear-tips are for single use only.
CAUTION