3
Table of Contents
1.1 Using this Instruction Manual .................................................................... 5
1.2 Icons...................................................................................................... 5
1.2.1 General Symbols ................................................................................. 5
1.2.2 Device and Packaging ........................................................................... 5
1.2.3 Display ............................................................................................... 6
1.3 Symbol Convention .................................................................................. 6
1.4 Glossary ................................................................................................. 7
1.5 Intended Use .......................................................................................... 8
1.5.1 Indications .......................................................................................... 8
1.5.2 Contraindications ................................................................................. 8
1.5.3 Precautions ......................................................................................... 8
1.5.4 Restrictions on use ............................................................................... 9
1.6 Basic Safety Instructions .......................................................................... 9
1.7 User Requirements .................................................................................11
1.8 Information on Product Liability ................................................................11
1.9 Material Compatibility ..............................................................................11
2.1 Whole View ............................................................................................12
2.1.1 PRO-II
®
Device ...................................................................................12
2.1.2 PRO-II
®
Device product contents ..........................................................12
2.1.3 Pro-III
®
Device ...................................................................................13
2.1.4 PRO-III
®
Device product contents .........................................................13
2.2 Product Properties ..................................................................................14
2.2.1 Disposable exudate canister for PRO-II
®
Device ......................................14
2.2.2 Information on the filter system for the PRO-II
®
Device ...........................15
2.2.3 Information on the carbon filter of the PRO-II
®
Device ............................15
2.2.4 Disposable exudate canister system for PRO-III
®
Device ..........................15
2.2.5 Information on the double filter system for PRO-III
®
Device .....................16
2.2.6 Battery ..............................................................................................16
2.2.7 Pressure settings ................................................................................17
2.3 Warranty ...............................................................................................17
3.1 Set-Up and Startup .................................................................................19
3.1.1 Startup ..............................................................................................19
3.1.2 Connecting the PRO-II
®
and PRO-III
®
Devices ........................................19
3.1.3 Positioning of the PRO-II
®
Devices ........................................................20
3.1.4 Connecting the disposable exudate canister of the PRO-II
®
Device ............20
3.1.5 Positioning of the PRO-III
®
Device .........................................................20
3.1.6 Connecting the DeRoyal
®
disposable exudate canister system of the PRO-III
®
Device ...............................................................................................21
3.1.7 Connecting a wound drainage system ....................................................21
3.2 Operation of the PRO-II
®
and PRO-III
®
Devices ..........................................22
3.2.1 Operation at initial startup ...................................................................22
3.2.2 Continuous operation ..........................................................................23
3.2.3 Intermittent operation .........................................................................24
3.2.4 Language selection .............................................................................26
3.2.5 Alarm delay at startup .........................................................................26
3.3 Patient Mode ..........................................................................................27
3.4 Canister exchange ..................................................................................29
3.4.1 Replacement of the canister of the PRO-II
®
Device ..................................29
3.4.2 Replacement of the canister of the PRO-III
®
Device ................................29
4.1 Cleaning and Care ..................................................................................30
4.1.1 General Information ............................................................................30
4.1.2 Cleaning and disinfection of the surface of the device ..............................30
4.1.3 Disposal of the exudate canister incl. the suction tube for PRO-II
®
Device ..31
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