User Manual
Table Of Contents
- 1 Safety and Regulatory Information
- Document Conventions
- Intended Use and Indications for Use
- Safety and Related Information
- DRX-1 System Product Information
- Disposal Information
- Operating Environment
- 2 Hardware and Operation
- Overview
- CARESTREAM DRX-1 System
- Cautions
- Installing the Hardware
- CARESTREAM DRX-1 System Battery
- Labeling the Detector
- DRX-1 Detector LED
- Positioning the Detector in the Bucky
- Range of Operation
- Wireless Operation
- Tether Operation
- Cleaning the Hardware
- With Each Occurrence of Patient Contact
- System Maintenance
1-6 7H8166
Safety and Regulatory Information
The following Product Safety Standards are applicable to the
CARESTREAM DRX-1 System Battery.
The following Product Safety Standards are applicable to:
• CARESTREAM DRX-1 System Battery Charger
• CARESTREAM DRX-1 System Console
• CARESTREAM DRX-1 System Wireless Access Point
USA UL 60601-1:2003 - Medical Electrical Equipment, 1st Edition
Canada CAN/CSA-C22.2 No. 601.1-M90 (R2001) Medical Electrical Equipment
CAN/CSA-C22.2 No. 601.1S1-94 (R1999) - Supplement No. 1-94 to
CAN/CSA-C22.2 No. 601.1-M90
CAN/CSA-C22.2 No. 601.1B-90 (R2002) - Amendment 2 to CAN/CSA-C22.2
No. 601.1-M90
Europe EN 60601-1:1990 + Amendment 1:1993 + Amendment 2:1995 - Medical
Electrical Equipment
International IEC 60601-1:1988 + Amendment 1:1991 + Amendment 2:1995 - Medical
Electrical Equipment
USA UL 60950-1, Information Technology Equipment - Safety - Part 1: General
Requirements
Canada CAN/CSA C22.2 No. 60950-1-03, Information Technology Equipment - Safety
- Part 1: General Requirements
Europe EN 60950-1:2001 + A11, Information Technology Equipment - Safety - Part
1: General Requirements
International IEC 60950-1:2001, Information Technology Equipment - Safety - Part 1:
General Requirements