Soleo
line
Service
Rev. B
26.07.10
-33-
K:\GRUPPE\QS\MDD-Doku\Service Handbuch soleoline.doc
12. Safety check
12.1. Soleo
line
Serial no. device : ........................................…
Serial no. of board……………………………….
Software version ...........................................
Visual inspection:
Visual check
O
ok
Fuses (2AT)
O
ok
Power switch and cable
O
ok
Internal wiring
O
ok
All screws present and tight
O
ok
Protective conductor present and tight
O
ok
Housing (no damage, labels legible, no dirt)
O
ok
Electrical safety:
Ground leakage current (max.500
µ
A)
O
ok
Ground leakage current 1st error (max.1000
µ
A)
O
ok
Housing leakage current (max.100
µ
A)
O
ok
Housing leakage current 1st error (max.500
µ
A)
O
ok
Patient leakage current (channel 1 max.100
µ
A)
O
ok
Patient leakage current 1st error (channel 1 max.500
µ
A)
O
ok
Patient leakage current (channel 2 max.100
µ
A)
O
ok
Patient leakage current 1st error (channel 2 max.500
µ
A)
O
ok
Patient leakage current (ultrasonic head max.100
µ
A)
O
ok
Patient leakage current 1st error (ultrasonic head max.500
µ
A)
O
ok
Function test:
Cable control both channels
O
ok
LCD display
O
ok
Touch screen
O
ok
Actuator
O
ok
Speaker
O
ok
Therapy clock
O
ok
Device test:
Program GA01 (80mA eff.-30%) Ch.1:…..….mA, Ch2:……..mA
Program NF00 (80mA peak(43mA eff.)-30% ) Ch.1:………mA, Ch2:…..….mA
Program MI03 (2mA peak(2 mA eff.)±30%) Ch.1:………mA, Ch2:….…..mA
Program MF01(100mA eff.±30%) Ch.1:……….mA, Ch2:….…..mA
Note:
The accuracy of the measuring equipment must be <5%!
A patient cable must be grounded during the function-current measurements!
Over-current interruption:
(Prog GA01, CV, short-circuit both patient clips, turn on of actuator)
therapy interruption
O
ok
Combined therapy (only with
Sonostim
)
O
ok
Ultrasonic emission (Start therapy, gel or water on the ultrasonic head, turn on of actuator)
O
ok
Coupling indication test at min and max output energy
O
ok
Therapy with Vaco device ( only with
Galva
or
Sonostim
)
O
ok
Test run with different parameter’s settings:
O
ok
All items checked
O
ok
Date:
_________________________________
Name:
________________________________
Signature:
_____________________________
Please observe the legal regulations for repairs and maintenance of medical devices in your country.