Instructions for use, ERGO 300 - BOWA- IFU-12930- ERG0300-S0-EN-20210701 3
Table of Content
1
General information
4
1.1 Indications
4
1.2
Principle
4
1.3
Contraindications
4
1.4
Target group
4
1.5
Medical application
5
1.6
On receipt
5
1.7
Scope of delivery, accessories and spare parts
6
1.8
Technical data: ERGO 300 – Morcellator
7
1.9
Ambient conditions
7
1.10
Warranty
7
1.11
Technical changes reserved
7
2
Explanation of symbols
8
3
Safety information
9
3.1
EMC, Manufacturer’s Declaration of Conformity
9
3.2
Modification and misuse
9
3.3
In the event of a serious incident
9
3.4
Essential requirements
10
3.5
During use
10
4
Device overview
11
4.1
System-Chart, ERGO 300 – Morcellator
13
5
Before use
14
5.1
Potential equalization connection according to DIN 42801
14
5.2
Connection to the power supply
14
5.3
Device preparation
14
5.3.1
Mounting the morcellator set with protective tube (according to
option 1
)
15
5.3.2
Assembly of the Morcellator set with Trocar Cannula (according to
option 2
) 18
5.3.3
Mounting a grasping forceps (according to
option 3
)
21
5.4
Mains connection
21
6 Operation
22
6.1
Using the control unit
22
6.2 Execution
24
6.2.1
Option 1: Morcellation with protective tube
26
6.2.2
Option 2: Morcellation with Trocar Cannula
27
6.2.3
Option 3: Myomektomy
29
6.3
After use
30
6.4
Disassembly of the Trocar Cannula
31
6.5
Disassembly of the motor
32
6.6
Disassembly of gear unit and Morcellator with protective tube
32
7
Instrument preparation
33
7.1
Control unit and pedal
33
7.2
The following instruments must be reprocessed
34
8
Maintenance and repair
38
8.1
General maintenance
38
8.2
Replacing the control unit fuse
39
8.3
Safety inspections
39
8.4
Malfunction and troubleshooting
40
8.5
Fault messages on the display
41
8.6
Spare parts list with order number
42
8.7
Information on disposal
42
Appendix
43
Electromagnetic Compatibility (EMC)
44
Declaration of Conformity
47
Manufacturer and service points
49
Содержание ERGO 300
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