
Q9 Digital Color Doppler Ultrasound System
Regulatory Requirement
This product conforms to the essential requirements of the Medical Device
Directive 93/42/EEC. Accessories without the CE mark are not guaranteed to
meet the Essential Requirements of the Medical Device Directive.
This manual is a reference for the Q9. Please verify that you are using the latest revision of this
document. If you need the latest revision, contact your distributor.
Important
1.
No part of this manual may be reduced, modified, copied or reprinted, in whole or in part, without
written permission from CHISON.
2.
The contents of this manual are subject to change without prior notice and without our legal
obligation.
3.
Before operating the system, please read and understand this manual. After reading, keep this
manual in an easily accessible place. If you have any question or doubt, please contact CHISON's
authorized service engineer.