Inhaltsverzeichnis - Depuy Synthes CODMAN NEURO DirectLink ICP Module Betriebsanleitung

Table of Contents
IMPORTANT INFORMATION ........................................... 3
Description ....................................................................... 3
Indications ........................................................................ 3
Contraindications ............................................................ 3
User Profile ...................................................................... 3
WARNINGS ....................................................................... 3
PRECAUTIONS ................................................................ 3
Electrostatic Discharge (ESD) Information ................... 3
List of Symbols ................................................................ 3
Instructions for Use ......................................................... 4
Materials Required ........................................................ 4
A. Connect the DirectLink Module to the Patient
Monitor ..................................................................... 4
B. Calibrate the Patient Monitor ................................... 4
C. Zero the ICP Sensor ................................................. 4
D. Implant the Sensor ................................................... 5
E. Disconnect the Sensor During Patient Transport .... 5
F. Resume Monitoring After Temporary
Disconnection (ACKNOWLEDGE Function) .......5
G. Connect an Implanted Sensor to a Different
Monitor ..................................................................... 5
H. Discontinue Monitoring ICP / Wipe Down and
Inspect the System ................................................... 5
Sterilization ...................................................................... 6
Storage ............................................................................. 6
Technical Specifications ................................................. 6
Operating conditions .................................................... 6
Output Signal ................................................................ 6
Power Consumption ..................................................... 6
Transducer Compatibility .............................................. 6
Patient Monitor Connection .......................................... 6
Recommended External Patient Monitor
Specifications ........................................................... 6
Applicable Standards ...................................................... 6
Recommended Accessories and Reordering
Information ....................................................................... 6
Troubleshooting ............................................................... 6
Maintenance .................................................................... 7
Service and Repair .......................................................... 7
Product End of Life .......................................................... 7
Warranty ........................................................................... 7
Appendix A ....................................................................... 7
Electromagnetic compatibility ...................................... 7
General Notes ............................................................. 7
Table 1 Guidance and manufacturer's declaration -
electromagnetic emissions ......................................... 7
Table 2 Guidance and manufacturer's declaration -
electromagnetic immunity .......................................... 7
Table 3 Guidance and manufacturer's declaration -
electromagnetic immunity .......................................... 8
Table 4 Recommended separation distances
between portable and mobile RF communications
equipment and the DirectLink .................................... 8
2