Roche Diagnostics
Operator’s Manual · Version 3.1 A-3
Cedex Bio System 1Safety
Table of contents
Safety
Protecting yourself and the environment
In this chapter, you will find information on the safe operation of the Cedex Bio
instrument.
Safety classification ......................................................................................................... A–5
Safety information ........................................................................................................... A–5
Transport ................................................................................................................... A–5
Electrical safety .......................................................................................................... A–5
Optical safety ............................................................................................................. A–6
Mechanical safety ...................................................................................................... A–6
Instrument covers ..................................................................................................... A–6
Operation and maintenance .................................................................................... A–6
Biohazardous materials ............................................................................................ A–6
Waste ..........................................................................................................................A–7
Reagents and other working solutions ................................................................... A–7
Installation ................................................................................................................. A–7
Environmental conditions ....................................................................................... A–7
Power interruption ................................................................................................... A–8
Electromagnetic devices ........................................................................................... A–8
Approved parts .......................................................................................................... A–8
Third-party software ................................................................................................ A–8
Operator qualification .............................................................................................. A–9
Operation over an extended period of time .......................................................... A–9
Cross contamination of sample .............................................................................. A–9
Insoluble contaminants in sample .......................................................................... A–9
Spillage ........................................................................................................................ A–9
Data security ..................................................................................................................A–10
Disposal recommendation ........................................................................................... A–11
Disposal label ........................................................................................................... A–11
Disposal of external components ......................................................................... A–11
Disposal of the instrument .................................................................................... A–11
Constraint ................................................................................................................ A–12
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