User's Manual
Table Of Contents
- Introduction and Basics
- Introduction
- Safety Information
- Installing and Moving Sprite
- Safety
- External Machine Diagram
- Machine Specifications
- Contact Information
- Basic Operation
- Sample Placement
- Contact Information
- Components
- Main Screen
- Begin a New Scan Screen
- Scanning Screen
- Scan Review Screen
- Processing Setup Screen
- Results Screen
- _
- Locate a Scan Screen
- Background Processing Screen
- Utilities Screen
- System Sleep Button
- Touch screen Calibration Button
- System Shutdown Button
- Storage Device Management Button
- Network Configuration Button
- One Touch Scan Setup Button
- Submit Trouble Ticket Button
- Reset Processing Engine Button
- Reset System Board Service Button
- Reset X-ray Service Button
- Reset Scan Engine Button
- System Restart Button
- System Status Screen
- X-ray System Maintenance Screen
- Common Elements
- Technical Support
Introduction and Basics
Safety
Compliance
Sprite complies with all federal regulations for cabinet X-ray equipment set forth in the Code of
Federal Regulations (revised 2008) by the U.S. Food and Drug Administration's Center for
Devices and Radiological Health (see 21CFR1020.40). Sprite also complies with UL 61010-1
(Electrical Equipment for Measurement, Control, and Laboratory Use; Part 1: General
Requirements, Underwriters Laboratories). This Class A digital apparatus complies with
Canadian ICES-003. [Cet appareil numerique de la classe (*) est conforme a la norme NMB-003
du Canada.]
Modification of Sprite
FCC ID: DGFESPE130
IC: 458A-ESPE130
Modifications to this device shall not be made without the written consent of the 3M Company.
Unauthorized modifications may void the authority granted under federal Communications
Commission and Industry Canada rules permitting the operation of this device.
Please be advised that the U.S. Food and Drug Administration's Code of Federal Regulations for
ionizing radiation emitting products states:
"The modification of a cabinet X-ray system previously certified pursuant to 1010.2 by any
person engaged in the business of manufacturing, assembling or modifying cabinet X-ray
systems shall be construed as manufacturing under the act if the modification affects any
aspect of the system's performance for which this section has an applicable requirement.
The manufacturer who performs such modification shall recertify and reidentify the system
in accordance with the provisions of 1010.2 and 1010.3 of this chapter."
U.S. Food and Drug Administration. Code of Federal Regulations. 2008.
Title 21, Volume 8. 21CFR1020.40.
This equipment has been tested and found to comply with the limits for a Class A digital device,
pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection
against harmful interference when the equipment is operated in a commercial environment. This
equipment generates, uses, and can radiate radio frequency energy and, if not installed and used
in accordance with the instruction manual, may cause harmful interference to radio
communications. Operation of this equipment in a residential area is likely to cause harmful
interference in which case the user will be required to correct the interference at his own
expense.
Safety Features
Emergency Stop Button
Pushing this button physically disconnects the power to both the X-ray source and the
motion stages. This button is located on the front of the top door.
X-ray Shutoff Buttons on the Touch Screen
You may stop a scan by tapping the Abort button or by holding down the Turn X-rays Off
button (or, as mentioned above, by pressing the Emergency Stop button located on the
front of the top door.
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