Preparation Of Parts For Sterilization; Detailed Manual And Automatic Protocols; Information Concerning The Sterilization; Recommendations For The Inspection Of Parts - Ultradent Products ultrawave J58349 Manuel De L'utilisateur

• preparation of parts for sterilization;

• detailed manual and automatic protocols;

• information concerning the sterilization;

• recommendations for the inspection of parts.

Please refer to the User Manuals, Quick Start Guides and Quick Clean Guides for each
medical device for information about the following:
• unpacking and installing the medical device;
• using the medical device;
• monitoring and maintaining the medical device;
• technical specifications for the medical device

1 Documentation

This document contains the following information:

• relating to patient, practitioner and environmental safety;
• required to install your medical device in optimum conditions;
• required to contact the manufacturer or the latter's representatives if necessary;

1.1 Electronic documentation

The user instructions for your device are in part provided in electronic format and in part in printed format.
However, you can request a free printed copy of the user instructions via the website, by telephone or in
writing.
The electronic user instructions are available in PDF format (Portable Document Format) and you will need to have a
PDF file reader software installed to read the instructions.
The device user instructions can be consulted at the following addresses: www.ultradent.com and
www.satelec.com.
It is important for you to have read and understood the content of the user instructions relating to the use of your
device and its accessories prior to use.
We recommend that you visit the website regularly to consult and/or to download the latest version of your device's
user instructions.

1.2 Archiving duration

Users are asked to keep documentation on hand so that it can be consulted when necessary. You are asked to print
and/or to download all documents or sections of documents that you may need to consult in the event of an emergency,
if you are unable to connect to the internet or if your electronic display tool is not working (computer, tablet, etc.).
All printed and electronic format documentation relating to your medical device must be kept for the device's entire
service life. When loaning out or selling the medical device, the documentation must be provided with it.

2 Required information

2.1 Latest document update

12/2013

2.2 Official Texts

This medical device complies with the essential requirements of European Directive 93/42/EEC. This
equipment is designed and developed in compliance with Electrical Safety standard IEC60601-1 in force. It was
designed and manufactured in accordance with an EN ISO 13485-certified quality assurance system.
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J00039 • V3 • (13) • 12/2013 • RB77US030D
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