Keeler Jazz Ultra, Инструкция по эксплуатации

Страница: 4 / 20

2
EN
Jazz Ultra Instruments by KEELER
Consult instructions for use General warning sign
Date of manufacture Warning: Electricity
Manufacturer’s name and
address
Warning: Floor level obstacle
Country of manufacture
Warning: Non-ionizing
radiation
Waste Electrical and Electronic
Equipment (WEEE) recycling
Warning: Optical radiation
This way up Warning: Hot surface
Keep dry Conformité Européene
Fragile Type B applied part
Do not use if package is
damaged
Class II equipment
Temperature limit
Atmospheric pressure
limitation
Authorised representative in
the European Community
Humidity limitation
Catalogue number Serial number
Translation Medical device
The Keeler Jazz Ultra Instruments are designed and built in conformity with Directive 93/42/EEC, Regulation (EU)
2017/745 and ISO 13485 Medical Devices Quality Management Systems.
Classifi cation: CE: Class I
FDA: Class II
The information contained within this manual must not be reproduced in whole or part without the manufacturer’s
prior written approval. As part of our policy for continued product development we the manufacturer reserve the right
to make changes to specifi cations and other information contained in this document without prior notice.
This IFU is also available on the Keeler UK and Keeler USA websites.
Copyright © Keeler Limited 2021. Published in the UK 2021.