General Warning; Important Safety Rules - Moretti LEM Aspimed 2.2 Manual De Instrucciones

ASPIMED 2.2 Surgical aspirator is a portable unit, working with 230V ~ / 50 Hz network electricity, designed for the aspiration of bodily
fluids in adult and children. It's particularly suitable for nasal, oral or tracheal aspiration of mucus, catarrh or blood after minor surgical
procedures and can be used in post-operative therapy at home or conveniently transported from one hospital ward to another.
Easily portable equipment designed for continuous use.
Made of highly heat resistant, electrically insulated plastic material in conformity with the latest European
safety standard, the product is supplied with a complete polycarbonate autoclavable jar with overflow valve and it is equipped with
aspiration regulator and vacuum indicator located on the front panel.
READ INSTRUCTION MANUAL CAREFULLY BEFORE USE
ONLY HIGHLY QUALIFIED STAFF USE RESERVED
THE INSTRUMENT MUST NOT DISASSEMBLED
FOR TECHNICAL SERVICE ALWAYS CONTACT MORETTI S.p.A.
1. Check the condition of the unit before each use. The surface of the unit should carefully inspected for visual damage. Check the
mains cable and do not connect to power if damage is apparent;
2. Before connecting the appliance always check that the electric data indicated on the data label and the type of plug used,
correspond to those of the mains electricity to witch it's to be connected;
3. If the plug supplied with the appliance is incompatible with the mains electricity socket, contact qualified staff for replacement of
the plug with a suitable type. The use of simple or multiple and / or extension adapters is not generally recommended. Whenever
their use is indispensable, use those in compliance with safety regulations, however paying attention not to exceed the maximum
power supply limits, which are indicated on the adapters and extensions;
4. Respect the safety regulations indicated for electrical appliances and particularly:
•
Use original components and accessories provided by the manufacturer to guarantee the highest efficiency and safety of
the device;
•
The device can be used only with the bacteriological filter;
•
Never immerge the appliance into water;
•
Place instrument on stable and flat surfaces;
•
Position the device in a way that the air inlets on the back aren't obstructed;
•
Don't use in the presence of inflammable substances such as anaesthetic, oxygen or nitrous oxide;
•
Don't touch the device with wet hands and always prevent the appliance coming into contact with liquids;
•
Keep off the reach of children or not capable people without supervision;
•
Don't leave the appliance connected to the power supply socket when not in use;
•
Don't pull the power supply cable to disconnect the plug remove the plug from the mains socket correctly;
•
Preserve and use the medical device in environments protected from atmospheric factors and at a distance from heat
sources;
•
Don't use the device thoracic drainage.
For repairs, exclusively contact technical service and request the use of original spare parts.
5.
Failure to comply with the above can jeopardise the safety of the device;
6. Use only for the purpose intended. Don't use for anything other than the use defined by the manufacturer.
The manufacturer will not be responsible for damage due to improper use or connection to an electrical system not complying
with current regulation.
7. Particular precautions must be made concerning electromagnetic compatibility. The medical device must be installed and used
according to information supplied with the accompanying documents;
8. Instrument and accessory discharging must be done according to current regulations in the country of use.
9. None of electric or mechanical parts have been designed to be repaired by customers or end-users. Don't open the device, do not
mishandle the electric / mechanical parts. Always contact technical assistance
10. Using the device in environmental conditions different than those indicated in this manual may harm seriously the safety and the
technical characteristics of the same.
The manufacturer cannot be held liable for accidental or indirect damages should the device be modified, repaired
without authorization or should any of its component be damaged due to accident or misuse.
Any minimal modification / repair on the device voids the warranty and does not guarantee the compliance with the
technical requirements provided by the MDD 93/42/EEC (and subsequent changes) and its normatives.

GENERAL WARNING

IMPORTANT SAFETY RULES

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