Instruction manual
-3-
DORO
®
Instruction Manual
1. Conformities ....................................................................... 4
1.1 Guidelines and norms .........................................................4
1.2 CE conformity ......................................................................4
1.3 FDA Registration .................................................................4
2. General Safety Information ................................................4
2.1 Symbols used for safety information ...................................4
2.2 Proper handling and permitted user .................................... 6
2.3 Creutzfeldt Jakob Disease ..................................................6
3. Basic Information ...............................................................6
3.1 Warranty and liability ........................................................... 6
3.2 Obligations of the purchaser ...............................................6
3.3 Use as per instructions ........................................................7
3.4 Improper use .......................................................................7
4. Product description ............................................................8
4.1 General description/Intended use .......................................8
4.2 Component description .......................................................8
4.3 Components ........................................................................ 8
4.4 Technical specications .....................................................10
5. Mounting .......................................................................... 11
5.1 Mounting of the DORO Base Unit ..................................... 11
5.1.1 Adjusting the Base Unit to a standard OR Table ......... 11
5.1.2 Mounting the Base Unit to a standard OR Table ..........12
5.2 Mounting the DORO Swivel Adaptor ................................. 13
5.3 Mounting of the DORO Skull Clamp..................................13
5.4 Mounting of the DORO Skull Pins ..................................... 13
6. Use and Handling .............................................................14
6.1 Detailed description of application.....................................14
6.2 Function and safety inspection ..........................................19
6.2.1 Prior to clinical use of a DORO device ......................... 19
6.2.2 After clinical use of a DORO device ............................. 19
7. Care ................................................................................20
7.1 Manual Precleaning...........................................................20
7.2 Automated Cleaning .........................................................21
7.3 Sterilization ........................................................................22
7.4 Lubrication .........................................................................24
8. Maintenance and Repair ................................................. 25
8.1 Maintenance intervals .......................................................25
8.2 Maintenance to be performed by the purchaser................26
8.2.1 Adjusting the Locking Lever .......................................... 26
8.2.2 Checking the stability of the Transitional Member ........ 27
8.2.3 Replacing the Transitional Member .............................. 27
9. Environmentally Compatible Disposal ............................. 29
10. Manufacturer information .................................................29