GA_Portio-Koagulator_E_150914.docx
Page 3 of 44
Table of Contents
1
General Information
5
1.1
Preamble ........................................................................................................... 5
1.2
Scope of this User Manual ................................................................................. 5
1.3
Icons in this user manual ................................................................................... 6
1.4
Abbreviations in this user manual ...................................................................... 6
2
Saftey
7
2.1
Icons and symbols on the medical product ........................................................ 7
2.2
Icons and symbols on the packaging ................................................................. 8
2.3
Danger ............................................................................................................... 9
2.4
Warnings ......................................................................................................... 10
2.5
Cautions .......................................................................................................... 11
2.6
Notes ............................................................................................................... 14
3
Product Description
15
3.1
Intended Use / Purpose ................................................................................... 15
3.2
Indication/Contraindication .............................................................................. 15
3.3
User group ....................................................................................................... 15
3.4
Operating principle ........................................................................................... 16
3.5
Variants of the medical product ....................................................................... 16
3.6
Literature ......................................................................................................... 16
3.7
Components of the medical product ................................................................ 17
4
Putting into operation
20
4.1
Kind of Delivery................................................................................................ 20
4.2
Scope of delivery ............................................................................................. 21
4.3
Conditions for operation ................................................................................... 21
4.4
Assembling ...................................................................................................... 22
4.4.1
Connection of Instrument Cable 3 and Therapy Probe 4 ........................... 22
4.5
First putting into operation ............................................................................... 22
4.5.1
Connection to the equipotential bonding .................................................... 23
4.5.2
Connection to the power supply................................................................. 23
4.6
Functional Test ................................................................................................ 25
5
Operation
27
5.1
Switch ON the CerviX Coagualtor 6001 ........................................................... 27
5.2
Start of Coagulation Procedure ....................................................................... 28
5.3
Termination of the Treatment .......................................................................... 29
6
Hygienic measures
30