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Cautions for Use
This monitor is designed to perform in conformity with the description thereof contained in this operation
manual when operated, maintained and repaired in accordance with the instructions provided. The monitor
should not be modified in any way. Ensure pressure compatibility for all patients. If any abnormality occurs in
the monitor, suspend the operation immediately and disconnect it from the patient. If the monitor has been
used or stored outside its acceptable range (see Specifications page), it may not meet performance specifi
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cations. If the cuff fails to deflate, the patient should be instructed on its proper and safe removal.
Warnings
The general warning sign indicates a potentially hazardous situation which could result in serious injury.
WARNING:
Do not use in the presence of flammable anesthetics; this could cause an explosion. This device
is not suitable for use in an oxygen enriched environment.
WARNING:
Do not immerse the monitor in any fluid, place fluids on top, or attempt to clean the monitor with
any liquid detergents, cleaning agents, or solvents. This may cause an electrical hazard. Do not use the mon
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itor if accidental wetting occurs; please return to SunTech Medical (see Limited Warranty). Refer to Maintain
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ing and Cleaning the Oscar 2 ABP System, for care instructions.
WARNING:
Too frequent measurements can cause injury to the patient due to blood flow interference.
WARNING:
The cuff should not be applied over a wound as this can cause further injury.
WARNING:
The cuff should not be placed on the arm on the side of a mastectomy. In the case of a double
mastectomy use the side of the least dominant arm.
WARNING:
Pressurization of the cuff can temporarily cause loss of function of simultaneously used monitor
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ing equipment on the same limb.
WARNING:
Do not use if device is dropped and/or is damaged. Have a qualified service representative check
the monitor before using again.
WARNING:
Do not attach the cuff to a limb being used for IV infusions or any other intravascular access,
therapy or an arterio-venous (A-V) shunt. The cuff inflation can temporarily block blood flow, potentially caus
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ing harm to the patient.
WARNING:
Use only with the cuffs supplied by SunTech Medical. Different cuffs have not been validated with
Oscar 2 and measurements with non-validated components may not be accurate
WARNING:
Use of an ACCESSORY, transducer or cable with ME EQUIPMENT and ME SYSTEMS other than
those specified may result in increased EMISSIONS or decreased IMMUNITY of ME EQUIPMENT or ME SYS
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TEM.
WARNING:
The Oscar 2 may be interfered with by other equipment even if the other equipment complies
with CISPR Emission Requirements.
WARNING:
Performance can be affected by extremes of temperature, humidity and altitude.
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80-0062-00-RevL 2020-9-14