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Dräger BiliLux User Manual
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72
Instructions for use BiliLux
T
echnical data
14.2.1
Spring arm dimensions
14.2.2
T
rolley dimensions
040
110°
120°
155°
10°
20°
155°
360°
6.1 cm
(2.4 in)
45.2 cm
(17.8 in)
45.2 cm
(17.8 in)
115°
115°
Ø22
041
126 cm (49.6 in) MAX
84 cm (33.1 in) MIN
48.4 cm
(19.1 in)
49.5 cm
(19.49 in)
35.1 cm
(13.82 in)
12.0 cm
(4.7 in)
MAX
71
73
Table of Contents
Default Chapter
3
Table of Contents
3
1 Information about this Document
7
Typographical Conventions
7
Illustrations
7
Use of Terms
7
Trademarks
7
2 Safety-Related Information
9
Target Groups
9
Information on Safety Instructions and Precautionary Statements
10
Basic Safety Instructions
11
Device Compatibility Safety
13
Safety Instructions for Accessories
13
Electrical Safety
14
Explosion and Fire Protection
15
Drug Storage Precautions
15
Mechanical Safety
16
Device Failure
16
3 Application
17
Intended Use
17
Environment of Use
17
Indications/Contraindications
17
4 Overview
19
Bililux Phototherapy Light
19
Bililux with Optional Spring Arm
20
Bililux with Optional Trolley
21
Radiometer (Optional)
22
Description
22
Abbreviations
23
Definitions
24
Symbols
24
5 Operating Concept
27
Control Panel
27
Displaying Bililux Screens
28
Adjusting the Bililux with Spring Arm
29
6 Assembly and Preparation
31
Unpacking
31
Proper Assembly
31
Placing the Bililux Phototherapy Light on an Incubator Hood
32
Installing the Bililux with Optional Spring Arm
32
Installing the Bililux with Optional Trolley
34
Installing the Optional Radiometer
35
7 Getting Started
37
System Startup
37
Functional Check Procedure
38
8 Operation
41
Positioning the Bililux
43
Adjusting Light Distance and Coverage for the Patient
47
Starting Therapy
48
Using the Bililux Radiometer (Option)
49
Exporting a Phototherapy Report
50
Checking Device Status
51
Ending Phototherapy
52
Using the MEDIBUS.X Interface for Data Transfer
52
Shutting down the Device
53
9 Configuration
55
Adjusting the Date and Time
55
Adjusting the Language
56
10 Troubleshooting
57
11 Reprocessing
59
Disassembly
59
Information on Reprocessing
59
Classifications for Reprocessing
60
Reprocessing List
61
Reprocessing Procedures
61
After Reprocessing
63
Preparations before Reuse
63
12 Service
65
Safety Information
65
Overview
66
Definition of Service Terminology
66
Inspection
66
Maintenance
67
Maintenance Instructions
67
Repair
68
13 Disposal
69
For Countries Subject to the EU Directive 2002/96/EC
69
14 Technical Data
71
Device Classification
71
Physical Attributes
71
Environmental Requirements
73
Electrical Requirements
73
Noise Requirements
73
RS-232 Communication Port
73
Irradiance
74
Radiometer Option Requirements
75
Device Combinations
76
EMC Declaration
76
15 List of Accessories
83
Device
83
Accessories
83
Optional Components
83
Index
85
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Dräger BiliLux Specifications
General
Brand
Dräger
Model
BiliLux
Category
Medical Equipment
Language
English
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