ED01_REV01-2020 IFU OB2012-2P_ENG
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Device application
sites according to
ISO 10079-1:2019
Suction units OB 2012 can be used in many situations: in hospitals/clinics, at sites of
accidents and emergency health services, for first aid in general, at home care and health
care facilities, for outdoor application and during transport.
2. WARNINGS, PRECAUTIONS AND IMPORTANT INFORMTION
Read carefully
These operating instructions have been prepared using simple, easy to understand language. If
you have difficulty interpreting what is written, please contact the manufacturer for further
clarification.
Phone +39 0471 93 28 93 info@boscarol.it
• Read these instructions carefully before using the device. Careful, correct use of the device ensures smooth
operation and will protect both patients and operators.
• The suction unit is designed exclusively to remove organic fluids (secretions) during medical procedures. For
this reason, it should only be used by properly trained personnel
• Never use the suction unit in the presence of flammable and/or explosive liquids, gases or anaesthetic
mixtures as this could result in explosion and/or fire.
• If suction is performed without the jar and/or antibacterial filter, or if you suspect that substances may have
entered the suction circuit (i.e., the OB 2012
device), contact your nearest service centre or the
manufacturer immediately to have the device checked.
• Do not spray substances on the device. Before cleaning the device, make certain that the suction hole on
the container is closed (cover it with a piece of tape or connect the tube to the jar).
• Before cleaning the suction unit or performing any maintenance, disconnect the unit from the external
power supply or from the wall bracket. Do not immerse the device in liquids since this could damage it and
cause the safety devices to trip.
• Suction unit OB 2012 requires no maintenance by the operator. The only authorized operations are those
indicated in these instructions. For technical support, periodic service and repairs, contact the authorized
service centre or the manufacturer.
• For authorized personnel — who have taken a specific technical training course — the manufacturer
provides the documentation and tools needed to perform all service operations (service manual).
• To ensure patient safety, accuracy of the values displayed and correct operation, use only original spare
parts. In the case of non-compliance, the operator is held responsible for any patient injury or property
damage.
• Do not use any batteries other than those approved by the manufacturer.
• Do not modify the mechanical or electrical parts of the support bracket. Replacing any parts of the wall
bracket and/or modifying the bracket itself can seriously affect safe anchoring of the device.
• Suction units OB 2012 do not perform any diagnostic functions on the patient.
LATEX
Devices OB 2012 are built and manufactured without the use of latex. However, the possibility
that they may have come into contact with latex at some time during the production chain cannot
be ruled out
Do not use the device in environments where magnetic resonance imaging is performed. The
device could be dangerous for users and patients
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