FujiFilm DR-ID 670, Руководство по эксплуатации

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DR-ID 670 Operation Manual 897N102735
Introduction
DR-ID 670 is an X-ray equipment which acquires a general radiograph from the indirect-conversion flat
panel sensor. The detector of flat panel sensors features 150 micron pixel pitch, a wide 16-bit dynamic
range and exposure times up to 3.8 seconds.
Intended Use
The Fujifilm DR-ID 670 provides digital image capture for radiographic examinations.
It is intended for use in general projection radiographic applications wherever conventional screen-film
systems or CR systems may be used. DR-ID 670 is a device that provides images, which diagnostic
image process is not implemented, to image collecting console. It is not designed for mammography,
fluoroscope, tomography or angiography.
About This Manual
This Operation Manual includes descriptions of matters necessary when using the DR-ID 670 such
as the equipment overview, operation procedures and precautions to observe, as well as daily
inspections and maintenance.
Refer System Operation manual (which describe about image correction console, and prepared by
System Integrator), about image collecting console and diagnostic images process.
Accompanying documents were originally drafted in the English language.
Important information
DR-ID 670 consists of DR-ID 600MP, DR-ID 670MC and DR-ID 601SE/DR-ID 602SE/DR-ID 611SE/
DR-ID 612SE/DR-ID 613SE.
DR-ID 601SE, DR-ID 602SE, DR-ID 611SE, DR-ID 612SE and DR-ID 613SE :Wireless communication
mode or wired communication mode is available. When used in wireless communication mode, an
access point*
1
, battery pack (optional) and battery charger (optional) are required.
*1 In the countries other than the U.S., an access point is not included as a component of the system.
For details including installation, consult our official dealer.
Each flat panel sensor complies with IEC 62220-1 (MEDICAL ELECTRICAL EQUIPMENT -
CHARACTERISTICS OF DIGITAL X-RAY IMAGING DEVICES - ) as a general X-ray radiography
equipment.
Installation may only be conducted by authorized service personal.
CAUTIONS
1. No part or all of this manual may be reproduced in any form without prior permission.
2. The information contained in this manual may be subject to change without prior notice.
3. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from
installation, relocation, remodeling, maintenance, and repair performed by other than dealers
specified by FUJIFILM Corporation.
4. FUJIFILM Corporation shall not be liable for malfunctions and damages of FUJIFILM Corporation
products due to products of other manufacturers not supplied by FUJIFILM Corporation.
5. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from remodeling,
maintenance, and repair using repair parts other than those specified by FUJIFILM Corporation.
6. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from
negligence of precautions and operating methods contained in this manual.
7. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from use
under environment conditions outside the range of using conditions for this product such as
power supply, installation environment, etc. contained in this manual.
8. FUJIFILM Corporation shall not be liable for malfunctions and damages resulting from natural
disasters such as fires, earthquakes, floods, lightning, etc.
This system is classified as a medical device under EC Directive 93/42/EEC.
Process waste correctly, as stipulated by local law or any regulations that apply.
Caution : Rx Only in the United States (Federal law restricts this device to sale by or on the order of
a physician.)