3A HEALTH CARE MINIASPEED Battery Evo Plus Manual De Instrucciones página 21

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with valve (2) are not used. The filter integrated in the bag also performs the function of preventing the return
of aspirated liquids towards the aspirator. In this case, to restore device operation, it is necessary to
replace the disposable bag. For the cleaning and disinfecting operations of the tubes (7-8) and vessel (1),
sterilise the single parts in an autoclave at a maximum temperature of 121° C, or by boiling for 10 minutes.
The bag is disposable and must always be replaced after every use. The bag must be completely inserted
in the vessel in order to prevent any vacuum losses.
N.B.: maximum disposable bag usage vacuum: – 0.75 bar (75 kPa).
4.2.1 Connection: connect one end of the short sterilisable silicon tube (7) to the yellow connector (VACUUM)
of the top (photograph 3b) and the other end to the "INLET" connector of the aspirator. Connect one end
of the long sterilisable silicon tube to the red connector (PATIENT) and connect the disposable sterile manual
regulator (11) and the disposable sterile cannula (10) to the other.
N.B.: only use the disposable bags supplied by 3A - Code 3A1687.
The MINIASPEED BATTERY EVO PLUS is fitted with a LED working light (10) which allows use of the device in
dark conditions and/or at night.
Press the button (11) to switch on the light, as shown in Figure 5 of page 3; press the button (11) again to switch
it off. The light switches off automatically after about 60 minutes.
The light is of LED type, so the amount of current it consumes is minimal and it can be used even during
treatment; however, it should be switched off whenever it is not required and/or at the end of the treatment.
N.B.: If using chemical disinfectants, follow the manufacturer's instructions exactly.
The cannula and the aspirated flow manual command are sterile, disposable products and must be replaced
after every application.
The antibacterial disposable filter must be replaced after every application.
Never leave the appliance in water or submerged; clean the external casing of the appliance using only a
damp cloth with detergent (non abrasive).
DESCRIPTION OF AMBULANCE MOUNTING / RELEASE SYSTEM
1.
Fit the bottom of the bracket fixed to the aspirator into the recess provided in the bottom of the bracket
mounted in the ambulance (as shown in Figure 6 of page 3).
2.
Keeping the device engaged with the bracket, push it until it engages with the hook in the top of the yellow
mobile bracket (as shown in Figure 6a):
N.B.: to ensure that the device engages correctly, press the mobile bracket, push the device fully down
and release the mobile bracket (as shown in Figure 6b).
ALWAYS CHECK THAT THE DEVICE HAS ENGAGED WITH THE BRACKET.
3.
To release the device, press the yellow mobile bracket and lift the aspirator up and towards you (as shown
in Figure 6c).
KEEP A FIRM GRIP ON THE HANDLE OF THE ASPIRATOR WHILE RELEASING IT.
DESCRIPTION OF PROCEDURE FOR MOUNTING BRACKET IN AMBULANCE
The ambulance mounting bracket is supplied assembled and complete (as shown in Figure 7):
1.
Wall mounting bracket.
2.
Mobile bracket.
3.
Mobile bracket spring.
4.
Block complete with electrical contacts and cord.
5.
2 metre power cord for connecting the ambulance battery.
Mounting the bracket in the ambulance
The bracket must be installed on the panel inside the ambulance by skilled staff authorised by the vehicle's
constructor/outfitter.
The fixing points are shown in Figure 7a, Figure 7b and Figure 7c.
M5 Allen screws (UNI 5931-DIN 912-ISO 4762) should be used since they undergo deceleration testing at
10g as required by the EN 1789 standard. Otherwise, screws (with the same mechanical characteristics)
having (non-tapered) heads, max. Ø10, and no more than 7 mm in height (including the washer, if fitted)
can be used.
DESCRIPTION OF USE OF WORKING LIGHT
CLEANING AND DISINFECTION OPERATIONS
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