HSD WellStore, Руководство пользователя

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ENGLISH
Troubleshooting
No intervention on the equipment is permitted, as in addition to generating
possible dangerous situations, it will invalidate the validity of the Warranty.
!
Caution
What to do if the appliance does not show any sign of operation
when the power switch is turned on?
Check that the power cable is properly inserted in its housing and in the
socket.
Check the power cable for signs such as:
- - breaks or interruptions;
- deterioration.
Check the integrity of the fuse inside the fuse holder.
!
Caution
In case of breakage or deterioration of the power cable, immediately
disconnect it from the power socket and replace it immediately.
After having turned on the general switch the appliance does not
enable the functions?
Check the treatment head connection.
Screw in the treatment head connector.
Select programme N. 114 ( PROBE TESTING ).
Turn on the START key and if no effect is noted, check that the “ PAUSE ”
and “ STOP ” led are off and that the “ ACTIVE ” led in on.
If the “ ACTIVE ” led is off, repeat the procedure.
If the “
ACTIVE
” led is on, check the emission of ultrasounds by allowing a
few drops of water to fall on the head; it will appear to move, seem to
fry and even evaporate slightly if the large knob is plugged in(see photo
below).
Reference regulations
Appliance has been produced in
compliance with the following
regulations:
• Directive 93/42/EEC, dated 14th
June 1993, regarding medical
appliances, adopted by Legislative
Decree no. 46 dated 24/02/97 and
its subsequent modifications.
CEI EN 60601-1
CEI EN 60601-1-2
CEI EN 60601-2-5
CEI EN 60601-1-11
CEI EN 14971
Declaration of conformity
The company HSD SRL, with registered and operational headquarters in
SERRAVALLE (RSM) in Strada Acqusalata, n 11 internal 6, declares,
under its sole responsibility, that the medical device called
risk class IIa in accordance with rule 9 of Annex IX of Directive 93/42 / EEC
and subsequent amendments (implemented in Italy with Legislative Decree
No. 46 of 24 February 1997, and subsequent amendments)
• complies with the essential requirements and provisions of Directive
93/42 / EEC and subsequent amendments and additions. as per the
Technical File filed at the Company;
• is manufactured in accordance with the Quality System that meets the
requirements set out in Annex V + VII of the aforementioned Legislative
Decree, as per the Certificate issued by BUREAU VERITAS ITALIA S.p.a.
- Notified Body n. 1370
– Viale Monza, n. 347 – 20126 Milan .
• complies with Directive 2011/65 / EU of the European Parliament and of
the Council of 8 June 2011, on the restriction of the use of certain
hazardous substances in electrical and electronic equipment.
•
the Authorized European Representative is Ms Manuela Corbelli Via
Boccioni n. 20- Morciano di Romagna
The legal representative
Manuela Corbelli
Serravalle (RSM)