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Precautions
Cautions
• No part of this product, including the infusion line, should be taken into or used in a control area for radiation devices/
MRI or inside a hyperbaric oxygen therapy room. If any part of this product is accidently brought into these environments,
immediately discontinue use. [This product is not designed to be used in these environments. Malfunction, damage or
degradation of this product may occur or it may lead to explosion.]
• During solution delivery, at a low flow rate in particular, do not move this product up or down. [The internal pressure level of
the infusion line changes due to gravity, which may cause excessive infusion or back-flow.]
• Since this product is precision equipment, it should not be used if it has received any impact (drop to floor, falling from
the IV pole, violent shock). [Even though no fault is observed in the product appearance, the original functionality or
performance (flow rate accuracy and various alarm functions, etc.) of this product may not be achieved, and therefore
inspection is required.]
• When purging a drug solution with high viscosity through a thin intravenous needle, an Occlusion alarm is likely to be
issued even if the infusion line is not occluded. A solution with high viscosity, deliver it at the rate of 100 mL/h or lower, not
by purging it. [If purging is continued, an Occlusion alarm may frequently be issued or the solution may be unable to be
delivered.]
• Use the drug solution after it has adjusted to the room temperature. [If the drug solution is used when it is still cold, it
interferes with the movement of the syringe (causing resistance of the plunger), frequently causing the Occlusion alarm to
be issued.]
• Use this product at the level of the patient's heart in a range of ±130 cm.
• When using this product together with other infusion systems, note that the alarm functions can be activated by one of
those systems.
• Since drug solution may cause a short circuit, ensure that the connecting sections of the AC inlet and AC power cable are
not wet when connecting. If moisture is present, ensure that the power is turned off and the AC power cable is removed
from both the pump and earthed AC power source, and then thoroughly wipe with a dry cloth. [Since this product does not
have a waterproof structure, it may affect the electrical components inside, and cause a malfunction.]
• Use an earthed AC power supply for normal use. The internal battery is an auxiliary power source for when the AC power
supply is not adequately available during transportation, power failure, etc.
• Before use, check the manuals of the medical supplies and medical equipment that are used in combination.
• This product should only be operated by skilled personnel.
• Regular inspections should be conducted. If any fault is observed, stop using this product and request an inspection and
repair. [The original functionality or performance of this product may not be achieved.]
• Attention is required not to apply any strong static electricity. [It may result in failure or malfunction.]
• Prior to first use, or if unused for a long period, connect this product to an earthed AC power supply and provide a
sufficient charge (8 hours or more) with the power turned off. [If not sufficiently charged, this product may not be able to
operate using the internal battery during a power failure, etc.]
• Even within the normal conditions of use, this product should not be used under conditions that cause a sudden
temperature change. [Condensation inside the product results in damage and time degradation, and therefore the original
functionality or performance of this product may not be achieved.]
• The AC power cable, communication or nurse call cable, used for this product should not be pinched with forceps or
equipment, e.g. caster, or punctured with a needle. [If a cable is damaged, electric shock or fire may occur. The original
functionality or performance of this product may not be achieved.]
• This product should not be used in a place where vibration, dust, mist, corrosive gas, etc., occurs or in a place where
the product is sprayed with liquid. If solution is spilled on this product, thoroughly wipe with a dry soft cloth. [The original
functionality or performance of this product may not be achieved, and it may cause a malfunction.]
• In a case where a manufacturer has made changes to their syringe, the flow rate accuracy and alarm function may not be
guaranteed. If any fault is observed, immediately stop using the product and contact TERUMO trained service technicians.
• When transporting with the pump fixed to the IV pole, do not hold the handle of the pump nor apply pressure from the top.
[The pole clamp may be dislocated or damaged.]
• When this product is transported while in use, do not touch the switches, etc. Use the keypad lock function as needed.
[Touching the switches etc. without the keypad lock enabled may result in an operation (power on/off, stop, start, rapid
infusion) that is not intended by this product.]
• The LCD and the Operation panel (switches etc.) of this product should not be pressed with excessive force and should not
be operated with a pointed object. [It may cause damage to or failure of the LCD or the Operation panel.]
• Do not disassemble, make alterations (including actions that interfere with the functionality or performance such as
taping the LCD or a movable part) to, or repair this product. [This may result in failure, damage or device performance
degradation of this product.]
Содержание TERUFUSION TE-SS730
Страница 104: ...104 X l l i Ph m Start 7 X c nh n v n ph m Start Ki m tra l u l ng VTBI v ti n h nh ti p t c truy n d ch...
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Страница 236: ...104 Troubleshooting Start switch 7 Confirm and restart Check the flow rate VTBI etc and resume the solution delivery...
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