
Table of contents
Instruction For Use • C-MAC® video laryngoscope 8401xxx, Electronic Module 8401/8402 X, C-MAC® PM 8401
XD • 96076011EN-US • V3.1
3
Table of contents
1 General information.......................................................................................................................................5
1.1 Reading the instructions for use ...............................................................................................................5
1.2 Scope........................................................................................................................................................5
2 Intended use .................................................................................................................................................6
2.1 Intended use .............................................................................................................................................6
2.2 Contraindications......................................................................................................................................6
2.3 Target user populations ............................................................................................................................6
2.4 User qualifications ....................................................................................................................................6
2.5 Safety precautions when using the C-MAC® video laryngoscope ...........................................................6
2.6 Safety precautions when using the C-MAC® PM .....................................................................................7
2.7 Training in the operation and function of the device ................................................................................7
2.8 Target patient populations........................................................................................................................ 7
3 Safety ............................................................................................................................................................8
3.1 Serious incidents ......................................................................................................................................8
3.2 Description of warnings ............................................................................................................................8
3.3 Unsterile instruments ................................................................................................................................8
3.4 Correct reprocessing ................................................................................................................................8
3.5 Risks due to damaged parts.....................................................................................................................8
3.6 Combination with other devices and accessories ....................................................................................9
3.7 Damage to the instrument ........................................................................................................................9
3.8 Damaged products ...................................................................................................................................9
3.9 Allergic reactions ......................................................................................................................................9
4 Product description ....................................................................................................................................10
4.1 Product overview ....................................................................................................................................10
4.2 Packaging symbols.................................................................................................................................12
4.3 Symbols on the product .........................................................................................................................12
4.4 Charging Unit for C-MAC® PM ...............................................................................................................12
5 Installation and commissioning...................................................................................................................14
5.1 Visual and functional test........................................................................................................................14
5.2 Initial operation .......................................................................................................................................15
5.2.1 Operating the C-MAC® PM.......................................................................................................... 15
5.2.2 Energy management.................................................................................................................... 17
5.2.3 Putting the electronic module into service .................................................................................. 18
5.2.4 Focus ........................................................................................................................................... 18
6 Application ..................................................................................................................................................19
6.1 Function keys for the video laryngoscope..............................................................................................19
6.2 Monitor function keys .............................................................................................................................19
6.3 Insertion of an oxygen or suction catheter (only with 8401 AX/BX/HX)..................................................19
6.4 Disassembly............................................................................................................................................20
6.5 C-MAC® bag 8403 YD ............................................................................................................................20
7 Reprocessing ..............................................................................................................................................21
7.1 Cleaning and disinfection .......................................................................................................................21
7.2 Manual cleaning and disinfection ...........................................................................................................22
7.3 Machine cleaning and disinfection .........................................................................................................22
7.4 Overview table ........................................................................................................................................23
7.5 Sterilization .............................................................................................................................................23
8 Service and repair .......................................................................................................................................25
8.1 Servicing and repair program .................................................................................................................25
8.2 Complaint shipments ..............................................................................................................................25
9 Limitation of Liability ...................................................................................................................................26