EN
3
Contents Page
1. Warning, Precautions and Notes ............................................................................................................ 5
2. Intended Use ............................................................................................................................... 6
3. System Parts ................................................................................................................................ 6
4. Contraindications........................................................................................................................... 7
5. Explanation of symbols used................................................................................................................ 7
6. Standards applied .......................................................................................................................... 8
7. Technical product specifications ............................................................................................................ 9
8. Ambu® aScope™ functions.................................................................................................................. 11
8.1 Ambu® aScope™ ..................................................................................................................... 11
8.2 Ambu® aScope™ Monitor............................................................................................................. 12
9. Connecting the system ..................................................................................................................... 14
9.1 Connecting to an external monitor/video recorder ................................................................................... 15
10. Clinical Application ......................................................................................................................... 15
11. Preparation for Use ......................................................................................................................... 15
12. Use of the Ambu® aScope™ system ......................................................................................................... 16
12.1 Injection and control of the Luer channel ............................................................................................. 17
12.2 Removal procedure .................................................................................................................. 17
12.3 Post-check guide..................................................................................................................... 17
12.4 Cleaning of the Ambu® aScope™ Monitor: ............................................................................................ 17
12.5 Disinfection of the Ambu® aScope™ Monitor ......................................................................................... 18
12.6 Disposal.............................................................................................................................. 18
13. Trouble-shooting guide..................................................................................................................... 18
14. Warranty and replacement program........................................................................................................ 18
Ambu® is a registered trademark of Ambu A/S, Denmark.
Ambu is certified according to ISO 9001 and ISO 13485.