Contents
1Introduction .....................................................................................................4
2Important information.....................................................................................5
2.1 Information about the device.............................................................................. 5
2.2 Intended purpose and classification................................................................... 5
2.3 Liability ............................................................................................................... 5
2.4 Scope of delivery................................................................................................ 6
3Safety instructions..........................................................................................7
4Set up, installation and reconditioning.........................................................8
5Operation.........................................................................................................9
5.1 Layout of the switches und buttons on the control console................................ 9
5.2 Commissioning................................................................................................... 9
5.3 Description and function of the components.................................................... 10
5.3.1 Translation table..............................................................................................................10
5.3.2 Patient chair ....................................................................................................................11
5.3.3 Phoropter arm .................................................................................................................11
5.3.4 Contact lens fitting table with trial lens tray .....................................................................11
6Care and maintenance..................................................................................12
6.1 Care.................................................................................................................. 12
6.2 Maintenance..................................................................................................... 12
6.3 Repairs that can be carried out by the user ..................................................... 12
6.3.1 Changing the bulb in the examination lamp ....................................................................12
6.3.2 Safety fuse ......................................................................................................................13
6.3.3 Function defects..............................................................................................................13
7Warranty.........................................................................................................14
8Technical data ...............................................................................................15
9Other information..........................................................................................22
Appendix: EC Declaration of conformity
3/23
