General Warning; Important Safety Rules - Ca-Mi NEW HOSPIVAC 400 Manual De Istrucciones

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NEW HOSPIVAC 400 / NEW HOSPIVAC 350 is a surgical aspirator power-fed at 230V ~ / 50Hz, to be used for suctioning body liquids (such as mucus,
phlegm and blood) provided with 4 antistatic wheels, two of which with braking device, and a pulling handle.
This equipment is designed for easy transport and continuous utilization.
Thanks to these characteristics and to its functions, this device is particularly suitable for utilization in hospital wards and operation theatres both for
suctioning body liquids and for gynaecological and dermatological (liposuction) applications.
It's provided with a plastic body, with thermal and electrical isolation in compliance with European safety standards, two complete suction tanks in
polycarbonate suitable for sterilization, and a float valve, besides being fitted with a suction regulator and a vacuum gauge on the front panel.
Versions fitted with footswitch control and flux deviator are available on request. The electronic management system fitted on the front panel allows to
perform suction by means of the footswitch control as well as to suction liquids in both tanks provided without having to switch the equipment off to
reconnect the second tank.
FULL CONTAINERS MUST BE HANDLED WITH GREAT CARE DURING TRANSFER TO THE DISPOSAL AREAS, FOLLOWING THE
1.
On opening the packaging, check the integrity of the appliance, paying particular attention to the presence of damage to the plastic parts, which may
make access possible to internal live parts and also to breakage and / or peeling of the power supply cable. In these cases don't connect the plug
to the electric socket. Carry out these controls before each use.
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 CA.MI. 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;
Avoid touching the aspirator with wet hands and always prevent the equipment from getting in touch with liquids. Never leave the equipment near
water or immerse it into a liquid. Should the equipment fall into water, detach its power cable from the socket before touching it;
None of the electrical and/or mechanical parts of the machine is designed to be repaired by the client and/or by its user. Do not open the
aspirator or disassembly its electrical and/or mechanical parts. Always report to CA.MI. snc technical support;
Using the equipment in environmental conditions other than those indicated in this manual may seriously endanger its safety and technical
parameters;
Position the appliance on flat stable surfaces;
Position the device in a way that the air inlets on the back aren't obstructed;
Never use the device in environments which have anaesthetic mixtures inflammable with air, oxygen or nitric 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.
5.
For repairs, exclusively contact CA-MI technical service and request the use of original spare parts. Failure to comply with the above can jeopardise
the safety of the device.
6.
This medical device must be destined exclusively for the use for witch it has been designed ad described in this manual. Any different use
must be considered incorrect and therefore dangerous; the manufacturer cannot be considered liable for damage caused by improper, incorrect and /
or unreasonable use or if the appliance is used in electrical plants that are not in compliance with the regulations in force.
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 accessories discharging must be done following current law regulations in every 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 CA.MI. 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.

GENERAL WARNING

READ INSTRUCTION MANUAL CAREFULLY BEFORE USE
ONLY HIGHLY QUALIFIED STAFF USE RESERVED
THE INSTRUMENT MUST NOT BE DISASSEMBLED
FOR A TECHNICAL SERVICE ALWAYS CONTACT CA-MI
KEEP OFF THE REACH OF CHILDREN OR NOT CAPABLE PEOPLE WITHOUT SUPERVISION
LOCAL PROCEDURES AND REGULATIONS

IMPORTANT SAFETY RULES

9

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