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Appendix
10. Symbols:
Confirm selection
Back
Scroll down (program selection)
Scroll up (program selection)
Start the highlighted program
Terminate the running program immediately
The conformity of the device with the relevant EU
directive 93/42/EWG MDD is validated through the
CE sign with the number of the identified post.
Refers to the necessity for the user to consult the
manual.
Device type BF according to IEC/EN 60601-1
Refers to the necessity for the therapist to consult
the manual in regard to important security related
statements, like warnings or cautionary alerts, which could not
be attached to the medical product directly for a variety of rea-
sons.
Indicates the manufacturer of the medical product
acoording to the EU guidelines 90/385/EWG,
93/42/EWG and 98/79.
32
0297
Содержание synapsis wave 2
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