Vitalograph Compact - Table of Contents

09220 Issue 2
3Page of 28
ENG
Vitalograph COMPACT - Instructions for Use
Contents
1. Indications for Use .............................................................................4
2. Contraindications, Warnings, Precautions
and Adverse Reactions ......................................................................4
3. Main Components of the Vitalograph Compact ..............................7
3.1. Features of the Vitalograph Compact ......................................8
4. Setting Up the Vitalograph Compact ................................................8
4.1. Compact Communications .......................................................9
5. Operating Instructions .......................................................................9
6. Power Management .........................................................................10
7. Cleaning & Hygiene ..........................................................................10
7.1. Preventing Cross-Contamination of Subjects ........................10
7.2. Inspection of the Vitalograph Compact .................................10
8. Fault Finding Guide ..........................................................................13
8.1. Software Check ........................................................................14
8.2. Product Useful Life Checks .....................................................15
9. Customer Service .............................................................................15
10. Consumables and Accessories ....................................................... 15
11. Disposal ............................................................................................16
12. Explanation of Symbols ...................................................................16
13. Description of the Vitalograph Compact ........................................17
14. TechnicalSpecication .................................................................... 18
15. CE Notice ..........................................................................................19
16. FDA Notice ........................................................................................22
17. EU Declaration of Conformity ..........................................................23
18. Guarantee .........................................................................................24