Kodak RVG, RVG 5100, RVG 6100 User Manual

CS4000-00_en
KODAK RVG Digital Radiography Systems
User’s Guide
Notice
© Eastman Kodak Company, 2006. No part of this publication may be reproduced, stored in a retrieval system, translated to another language, or transmitted in any form by any means, electronic, mechanical, photocopied, recorded, or otherwise, without prior written permission.
NEITHER EASTMAN KODAK COMPANY NOR ANY OF ITS SUBSIDIARIES MAKE ANY WARRANTY OF ANY KIND WITH RESPECT TO THIS MATERIAL, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY, NONINFRINGEMENT, AND FITNESS FOR A PARTICULAR PURPOSE.
The information in this document is subject to change. Neither Eastman Kodak Company nor any of its subsidiaries shall be liable for errors contained herein or for incidental damages in conjunction with the furnishing, performance, or use of this material.
Kodak and RVG are trademarks of Eastman Kodak Company. RINN is a trademark of Dentsply International, Inc. All other trademarks and registered trademarks are the property of their respective
holders.
Current Dental Terminology copyright © 2002, 2004 American Dental Association
U.S. Federal law restricts the Kodak RVG sensor to sale by or on the order of a dentist or physician.
Manual Name: KODAK RVG Digital Radiography Systems User’s Guide Part Number: CS4000_en Revision Number: 00 Print Date: June 2006
This document was originally written in English.
The names of persons and the data reflected in this guide are fictitious and are not intended to represent any real individual, event, or condition. Any resemblance or similarity of the names of persons or data reflected in this guide to any actual person’s name or any event or condition is purely coincidental and unintended.
Made in France by Kodak-Trophy A Subsidiary of Eastman Kodak Company Marne-la-Vallée, France
KODAK RVG Digital Radiography Sy stems User’s Guide (CS4000_en) iii
About This Guide
This manual contains information on using the following products:
KODAK RVG 5100 digital radiography sensor
KODAK RVG 6100 digital radiography sensor
The following list describes information contained in each chapter of this guide:
1 Compliance and Safety Describes compliance
information and indicates potential risks to personnel or equipment.
2 Getting Started Describes preliminary use of the
sensor .
3 Acquiring Images Describes the procedures for
acquiring images.
4 Disinfecting and
Maintaining the Sensor
Describes the procedures for disinfecting and maintaining the sensor.
5 Troubleshooting Images Describes techniques for
producing better images.
Note
Contact your Kodak dealer for any additional information you may need.
Foreword
iv About This Guide
Foreword
For optimum image display and processing quality, use the sensor with the Kodak dental imaging software. The Kodak dental imaging software is specifically designed to make the most of the capabilities of the sensor.
The sensor is a class I device in accordance with annex VII of directive 93/42/EEC concerning medical devices. The CE marking guarantees compliance with the main requirements of this directive.
A thorough review of this user guide is necessary to fully use the sensor.
KODAK RVG Digital Radiography Sy stems User’s Guide (CS4000_en) 1–1
Chapter 1
Compliance and Safety
This chapter includes the following topics:
Ensuring Compliance with Applicable Standards
on page 1–1
Directive 93/42/CEE Concerning Medical
Devices on page 1–2
Marking and Labeling Symbols on page 1–2
Non-Medical Devices on page 1–3
Ensuring Compliance with Applicable Standards
The electronics used in the sensor are designed to observe all applicable standards.
Do the following to ensure compliance with the applicable standards:
After installation, ensure that the system does not
represent any risk to the operator or patient.
Ensure all equipment associated with the system
bears a CE marking.
Check that the electrical network complies with
the current standards of the country of installation.
Directive 93/42/CEE Concerning Medical Devices
1–2 Compliance and Safety
Directive 93/42/CEE Concerning Medical Devices
The sensor belongs to class I of the Directive Concerning Medical Devices. The sensor is an active device that temporarily penetrates the body through a body orifice for diagnostic purposes. The applicable European standards are the General requirements for Safety (IEC/EN 60601-1 and collaterals) and Electromagnetic Compatibility (EN 60601-1-2).
Marking and Labeling Symbols
Table 1–1 describes the applicable marking and labeling symbols.
Table 1–1 Marking and Labeling Symbols
Label Description
Type BF Device
The sensor is a Type BF device.
WEEE Symbol
In the European Union, this symbol indicates that when the last user discards this product, it must be sent to appropriate facilities for recovery and recycling. Contact your local Kodak representative or refer to www.kodak.com/go/recycle for additional information on the collection and recovery programs available for this product.
Non-Medical Devices
KODAK RVG Digital Radiography Systems User’s Guide (CS4000_en) 1–3
Non-Medical Devices
Non-Medical Device Warning
This warning symbol means: “Warning: Consult the accompanying documents” and refers to this document. Using accessories that do not meet the equivalent sensor security requirements could result in a lower level of security for the entire system. When choosing an accessory , take into account its use around the patient and ensure that it complies with the harmonized standards IEC/EN 60 601-1 and IEC/ EN 60 601-1-1. Install and use computer or video peripheral equipment while closely following the steps in this manual to ensure compliance with these standards.
Non-Medical Devices
1–4 Compliance and Safety
KODAK RVG Digital Radiography Sy stems User’s Guide (CS4000_en) 2–1
Chapter 2
Getting Started
This chapter includes the following topics:
Understanding the Ima gi ng Chain on page 2–1
Adjusting Exposure Time on page 2–5
Sharing the Sensor Between Workstations on
page 2–9
Acquiring a Good Image on page 2–10
Enhancing the Digital Image on page 2–16
Understanding the Imaging Chain
The imaging chain consists of the following components:
Sensor and remote control
X-ray generator
Timer
Computer and monitor
Sensor and Remote Control
The sensor consists of two inseparable parts:
Sensor
Remote control
Note
To determine the exposure time and create an exposure time table for your sensors, see “Customizing the Exposure Chart” on page 2–7.
Note
Because these sensors are used in the same manner, this manual references use of the size 1 sensor.
Understanding the Imaging Chain
2–2 Getting Started
Sensor
Sensor
The sensor is radio-sensitive. The active surface is the flat surface marked with the Kodak logo. The marking #0, #1 or #2 indicates the size of the sensor, respectively size 0, 1, or 2. The back of the sensor, non-reactive to x-rays, is rounded and contains the cable attachment.
Remote Control
The use of your sensor depends on the kit ordered:
Size 1, universal, sensor—Use for regular
periapical and retro-coronary procedures.
Size 2 sensor—Use for bitewings and peri-apical
procedures.
Size 0 sensor—Use for pediatric intraoral exams.
The Size 0 sensor requires less x-ray doses and has a very small size to fit in a child’s mouth.
Remote Control
The remote control contains all the electronics of the sensor. The button on the remote control activates, at a distance, the acquisition in the Kodak dental imaging software. See “Preparing the Software” on page 2–10.
Understanding the Imaging Chain
KODAK RVG Digital Radiography Systems User’s Guide (CS4000_en) 2–3
The remote control is connected to the computer with its USB 2 connector . You can connect the remote control with the power on, when the computer is switched on. You do not need to start the Kodak dental imaging software before you connect the sensor. However, you can acquire the image only in the imaging module. You can disconnect the remote control with the power on, but do not disconnect the remote control when you are acquiring an image. This can damage the sensor.
X-ray Generator
The x-ray generator has a significant impact on image quality. Due to its high sensitivity and capacity to store an enormous quantity of inform ation, the sensor requires high-energy rays generated over very short time periods. This way , the im ages are formed by a ma ximum number of gray levels and you can process the images digitally to assist in extracting the clinical information. The Kodak generators meet the requirements.
As a general rule, the sensor is compatible with all generators provided the generator meets the current standard of intraoral radiology. You can use a high-frequency or conventional generator. The generator must operate with a voltage of 60 to 70kV.
The generator head must have a long cone with a focal point / film distance of at least 20 cm, to concentrate the x-rays toward the sensor. Select a mechanism that supports the generator and provides stability to avoid any motion blurring due to vibration of the x-r ay sou rce.
Caution!
See “Acquiring Images” on page 3–1 for the precautions to take when connecting and disconnecting the sensor in certain operating modes.
Important
The power of a generator decreases over time. Have the generator inspected annually to determine any difference between its nominal and effective power.
Important
The sensor is not compatible with generators of lesser specifications.
Understanding the Imaging Chain
2–4 Getting Started
Timer
Use the timer to control exposure times. Depending on the technologies used, the selected exposure time does not exactly represent the dose of x-rays output by the generator since the timing does not systematically take into account variations in the mains current. Avoid x-ray sources of inconsistent quality. Use a digital timer to compensate for current variations in conventional generators.
You can connect the Kodak generators directly to the electronics of the sensor to synchronize image acquisition with the trigger action. This link provides an ergonomic advantage that eliminates the need for the operator to click on the acquisition icon prior to each exposure. See “Preparing the Software” on page 2–10.
Remember that the image quality for short exposures is linked to the use of the physical synchronization function of the sensor and the timer, in particular with the very high-frequency Kodak intraoral x-ray units.
Adjusting Exposure Time
KODAK RVG Digital Radiography Systems User’s Guide (CS4000_en) 2–5
Computer and Monitor
Place the computer and its monitor in or close to the operating area, in the visual field of the practitioner when he is at the chair. Provide visual access for the patient, to encourage communication. This enables you to access the RVG system and maintain the working ergonomics at the chair.
Use a monitor with proper technical display characteristics for the visualization of radiologi cal images. Select and set up the monitor according to the procedure described in the installation guide for the sensor. Position the monitor to avoid direct light or reflections that could hinder the reading of the clinical information.
Adjusting Exposure Time
As in conventional radiology, the exposure time depends on the following:
Generator type
Patient's morphology
Tooth that is x-rayed
Caution!
A poor monitor setting or a poor quality monitor can cause diagnostic errors due to the inability of the equipment to display the image properly.
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