ENG
3Page of 40
09200 Issue 2
Vitalograph micro - Instructions for Use
Contents
1. Main Components .................................................................. 4
1.1. Features ................................................................. 5
2. Set Up ...................................................................................... 5
3. Operating the Vitalograph micro ............................................ 6
3.1. Entering Subject Data............................................ 6
3.2. Conducting a Test.................................................. 8
3.3. Reporting.............................................................. 12
3.4. Calibration Verication........................................ 13
3.5. Setting up a New Flowhead ................................ 15
3.6. Conguration Options ......................................... 16
4. Power Management in the Vitalograph micro..................... 21
4.1. Batteries ............................................................... 21
4.2. Power Save Mode................................................ 22
5. Cleaning & Hygiene ............................................................... 22
5.1. Preventing Cross-Contamination of Subjects.... 22
5.2. Inspection of the Vitalograph micro ................... 23
6. Remote Flowhead ................................................................. 23
7. Fault Finding Guide ............................................................... 24
8. Customer Service.................................................................. 26
9. Consumables and Accessories............................................ 26
10. Disposal ................................................................................. 27
11. Explanation of Symbols ........................................................ 27
11.1. Icons used in the Vitalograph micro .................. 28
12. Description of the Vitalograph micro................................... 31
12.1. Indications for Use............................................... 31
13. Technical Specication......................................................... 32
14. Contraindications, Warnings, Precautions and
Adverse Reactions ................................................................ 34
15. CE Notice ............................................................................... 36
16. FDA Notice............................................................................. 38
17. EU Declaration of Conformity............................................... 38
18. Guarantee .............................................................................. 39
