
06/2009 SM731_K2200_01_en
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1. Safety and Regulatory Information
The information contained in this manual is based on the experience and
knowledge relating to the subject matter gained by Carestream Health, Inc.
prior to publication. No patent license is granted by this information.
Carestream Health, Inc. reserves the right to change this information without
notice, and makes no warranty, express or implied, with respect to this
information. Carestream Health, Inc. shall not be liable for any loss or
damage, including consequential or special damages, resulting from any use
of this information, even if loss or damage is caused by Carestream Health,
Inc. negligence or other fault.
Conventions Used in This Manual
Note
Notes provide additional information,
such as expanded explanations, hints,
or reminders.
Important
Important highlights critical policy
information that affects how you use
this manual and this product.
CAUTION:
Caution points out procedures that you must follow precisely to avoid
damage to the system or any of its components, yourself or others,
loss of data, or corruption of files in software applications.
General Safety Guidelines
•
This product is designed and manufactured to ensure maximum
safety of operation. Operate and maintain it in strict compliance with the
safety precautions and operating instructions contained in this manual.
•
This product meets all the safety requirements applicable to medical
equipment. However, anyone attempting to operate the system must be
fully aware of potential safety hazards.
•
There are no user serviceable parts in this system. The product must
be installed, maintained, and serviced by qualified service personnel
according to procedures and preventive maintenance schedules in the
product service manual. If your product does not operate as expected,
contact your Service Representative.
•
Do not modify this product in whole or in part without prior written
approval from Carestream Health, Inc.
•
The assembly, extensions, adjustments, modifications, and repairs
must be performed by an authorized Service Representative. Your
radiology system must be installed in premises that comply with
applicable standards.
•
Personnel operating and maintaining this system should receive
training and be familiar with all aspects of operation and maintenance.
•
KODAK 2200 Intraoral x-ray system is intended to be used at the
direction of dentists, oral surgeons and orthodontists for x-ray imaging of
the dento-maxillo-facial area.
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