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AGFA DR 18M - Table of Contents

AGFA DR 18M
78 pages
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Contents
Legal Notice ..........................................................................4
Introduction to this Manual ................................................... 5
Scope .........................................................................6
About the safety notices in this document .................. 7
Disclaimer ................................................................. 8
Introduction to the DR Detector .............................................9
Intended Use ............................................................10
Indications for Use ................................................... 11
Intended User ..........................................................12
Configuration .......................................................... 13
Equipment Classification ..........................................14
Non-medical equipment ...............................14
Operation Controls .................................................. 15
DR 18M, DR 24M ......................................... 16
DR Detector Switch on the NX Workstation ....
17
DR detector cable and control unit ............... 18
System Documentation ............................................20
Training ...................................................................21
Product Complaints ................................................. 22
Compatibility ...........................................................23
Compliance ..............................................................24
General ........................................................25
Safety .......................................................... 25
Electromagnetic Compatibility .....................25
X-ray devices ................................................25
Connectivity ............................................................ 26
Wired communication ................................. 26
Installation .............................................................. 27
Environment of Use ..................................... 27
Messages ................................................................. 28
Labels ......................................................................29
Additional Labeling of the DR detector .........31
Additional Labeling of the DR detector control
unit ..............................................................32
Cleaning and Disinfecting ........................................ 33
Cleaning ...................................................... 34
Disinfecting ................................................. 35
Use of protective plastic envelope .................36
Approved disinfectants .................................37
Safety directions for disinfection .................. 38
Maintenance ............................................................40
Daily inspection ........................................... 41
Half-yearly inspection ..................................42
Patient data security ................................................ 43
ii
| DR 18M, DR 24M | Contents
0380A EN 20180703 1429

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