Bayer HealthCare MEDRAD MRXperion, Руководство по эксплуатации, Страница: 64 / 126

11 - 54 MEDRAD® MRXperion
Biological Contamination Hazard - Serious patient and/or worker injury or death may result.
Q
Properly discard contrast and saline containers and disposable items after use (refer to disposable label for specifics), or if there is
any possibility that contamination may have occurred.
Q
Do not reuse single-use fluid (contrast and saline) sources. Refer to the fluid source manufacturers’ instructions for use.
Q
Re-using contrast and saline containers for more than one procedure may result in biological contamination. Discard contrast and
saline containers after filling syringes for a single procedure.
Q
Bayer syringes and tubing sets are for single use only.
Q
Use of the system is intended to be consistent with contrast package labeling.
Environmental Contamination Hazard - Serious patient or worker injury or death may result.
Q
Follow aseptic technique when handling syringe and connector tubing components. Specifically, maintain sterility of all syringe
and connector tube components.
Q
Do not disassemble any syringe or connector tubing components. Do not remove the plunger from the syringe.
Q
Visually inspect contents and package before each use. Do not use if sterile package is opened or damaged.
Bacterial Contamination Hazard - Serious patient and/or worker injury or death may result.
Q
Syringes are not intended to be used as storage containers. Do not use syringes to store fluids. Use filled syringes immediately.
Mechanical Hazard - Serious patient injury could result from fluid leaks or tubing ruptures during an injection.
Q
Use only disposables or accessories supplied by Bayer. Refer to "Chapter 19 - Options and Accessories" for more information.
Q
Use only syringes and tubing with a pressure rating greater than the maximum programmable pressure limit of the injection
system, which is 325 psi (2241 kPa).
Q
Ensure that the fluid path is open and do not use syringes and tubing rated below 350psi (2410 kPa). An occlusion in the fluid path
and/or use of syringes or tubing rated below 350 psi (2410 kPa) may result in leaks or ruptures.
Q
Use catheters with pressure ratings compatible with this system. Refer to "Section 18.9.2 - Maximum Flow Rate Performance" and
"Section 18.5 - System Capabilities" for programmable pressure limit options.
Q
Patient injury and/or catheter damage may result from using tubing set that is too short. Operator must consider tubing length
and stretch limitations when moving the injector or the patient.
Adverse Reaction Hazard - Serious patient injury or death may result.
Q
Check the patient history for any evidence of allergy to injectable fluid sources.
Compromised Efficacy - Serious patient injury may result.
Q
Programming or loading an incorrect fluid source or concentration may result in patient injury or suboptimal imaging.
Patient injury could result from movement of the scan room unit (injector) after the patient is connected to the
fluid path.
Q
Do not move the Injector with the patient connected.
Q
Lock the casters at the base of the unit to prevent unintended movement.
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CAUTION
Mechanical Hazard - Minor or moderate patient and/or worker injury may result.
Q
Ensure the syringe is properly snapped into the front of the injector head before injecting. Improper engagement or rotating syringe
may cause the syringe to leak, to become damaged, or to come off during the injection, and can result in an under-volume delivery
and the syringe becoming a projectile.
WARNINGS