Haag-Streit OCTOPUS 900, Instructions For Use Manual

Page: 3 / 20

3
DEUTSCH ENGLISH FRANÇAIS ITALIANO ESPAÑOL NEDERLANDS
PORTUGUÊS
SVENSKA DEUTSCH ENGLISH FRANÇAIS ITALIANO ESPAÑOL NEDERLANDS
PORTUGUÊS
SVENSKA
© HAAG‑STREIT AG, 3098 Koeniz, Switzerland ‑ HS Doc. no. 1500.7220343.04070 – 7. Edition / 2016 – 11
Contents
1. Safety .......................................................................4
1.1 Areas of application of the device .........................................................4
1.2 Patient population .................................................................................4
1.3 Ambient conditions .................................................................................4
1.3 Shipment and unpacking .......................................................................4
1.4 Installation warnings .............................................................................4
1.4 Operation and environment ..................................................................4
1.6 Disinfection ............................................................................................5
1.7 Warranty and product liability .................................................................5
1.8 Symbols .................................................................................................5
2. Introduction ..............................................................6
2.1 Device description ..................................................................................6
2.2 System components ..............................................................................6
2.3 Device overview ....................................................................................6
2.4 LCD display ............................................................................................7
2.5 Control panel ..........................................................................................7
2.6 Connections ...........................................................................................7
2.7 Housing ..................................................................................................7
2.8 Cupola ....................................................................................................7
2.9 Forehead rest .........................................................................................7
2.10 Chin rest .................................................................................................8
2.11 Swing arm ..............................................................................................8
2.12 Refractive lens holder ...........................................................................8
2.13 Patient-response button .........................................................................8
2.14 Network connection ...............................................................................8
2.15 Light sources ..........................................................................................8
2.16 Light intensities ......................................................................................8
2.17 Stimulus .................................................................................................8
2.18 Periphery or background illumination .....................................................8
2.19 Fixation marks ........................................................................................8
2.20 Fixation control .......................................................................................9
2.21 Examination data ...................................................................................9
3. Appliance assembly / installation ..........................9
3.1 Transporting the appliance .....................................................................9
3.2 Connecting the patient response button ................................................9
3.3 Connect the network cable .................................................................10
3.4 Connect the electric power supply cable .............................................10
4. Safe system configuration in accordance
with EN 60601-1 .....................................................10
4.1 System variant I, Octopus 900 with
laptop as control unit ............................................................................10
4.2 System variant II, Octopus 900 with
PC and monitor as control unit ............................................................. 11
5. Commissioning ......................................................12
5.1 Switching on the appliance ..................................................................12
5.2 Switching off the appliance ..................................................................12
6. Operation ................................................................12
6.1 Setting up the patient ..........................................................................12
7. Software / Help menu / Error messages ..............12
8. Technical data ........................................................12
8.1 Octopus 900 .........................................................................................12
8.2 Infrared illumination ..............................................................................12
8.3 Field of sight ........................................................................................12
8.4 Octopus 900 control unit / PC ..............................................................13
9. Maintenance ...........................................................13
9.1 Repairs .................................................................................................13
9.2 Cleaning ...............................................................................................13
9.2.1 Cupola ..................................................................................................13
9.2.2 Response button, chin and forehead rest, eye occluder ......................13
9.2.3 Display, control panel ...........................................................................13
9.2.4 Light sources ........................................................................................13
A. Appendix ................................................................14
A.1 Accessories / spare parts .....................................................................14
B. Legal regulations ...................................................14
C. Classification .........................................................14
D. Disposal ..................................................................14
E. Standards ...............................................................14
F.
RoHS China ............................................................14
G. Information and manufacturer's declaration
concerning electromagnetic compatibility
(EMC) ......................................................................15
G.1 General ................................................................................................15
G.2 Emission (Standard table 1) .................................................................15
G.3 Immunity (Standard table 2) .................................................................16
G.4 Immunity for non-life-support devices (Standard table 4 ) ....................17
G.5 Recommended safe distances for non-life-support devices
(Standard table 6) ................................................................................18
01-IFU_Octopus900-7220343_04070_eng.indd 3 18.11.2016 14:03:36