GERATHERM 40600, Инструкция по эксплуатации

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Instructions for Use
Bodystik
Serial no.: xx|8|301|yyy and 2301xxxxx
Version: 7 | Release date: 02. August 2021 Page 5
9 Cleaning and Disinfection ....................................................... 84
9.1 Single Use .................................................................................... 85
9.2 Disinfection ................................................................................... 85
9.2.1 Flow Unit ...................................................................................... 88
9.2.2 Ergoflow / Flow Sensor................................................................. 88
9.2.3 Shutter System ............................................................................. 89
9.2.3.1 Shutter Cage or Shutter Block ...................................................... 89
9.2.3.2 Shutter Drive ................................................................................ 90
9.2.4 Bodystik / Cabin ........................................................................... 90
10 Fault Indication and Repair ..................................................... 91
11 Decommissioning / Disposal ................................................... 94
11.1 Expected Service Life ................................................................... 94
11.2 Decommissioning ......................................................................... 94
11.3 Disposal ....................................................................................... 94
11.3.1 Transport Packaging .................................................................... 94
11.3.2 Bodystik ....................................................................................... 94
11.3.3 Patient Chair ................................................................................. 95
11.3.4 Infectious / Contaminated Single Use Items ................................. 95
12 Technical Specifications ......................................................... 96
12.1 Technical Data .............................................................................. 96
12.2 Installation and Operating Conditions ........................................... 98
12.3 Electrical Safety Concept .............................................................. 99
12.3.1 Bodystik with Medical Device Cart and Isolation Transformer ....... 99
12.4 Electromagnetic Compatibility / EMC Guidelines ........................ 100
12.4.1 Emitted Interference Guideline and Manufacturer Declaration ..... 100
12.4.2 Interference Resistance for all ME Systems Guideline and
Manufacturer Declaration ........................................................... 101
12.4.3 Interference Resistance for Non-Life-Supporting ME Systems
Guideline and Manufacturer Declaration ..................................... 102
12.4.4 Recommended Safety Distances for Non-Life-Supporting ME
Systems ..................................................................................... 105
13 Safety of Product and Material .............................................. 106
14 Product Labeling / Type Label .............................................. 107
15 Warranty and Service ........................................................... 108
15.1 General Conditions ..................................................................... 108
15.2 Warranty Exemption ................................................................... 108
15.3 Packaging and Shipping ............................................................. 109
16 Authorised Specialist Retail Partner ...................................... 110