Terumo CAPIOX FX 25 Mode D'emploi page 14

12. Record the time drainage into the reservoir begins.
WARNING It is recommended that autotransfusion continue no longer than 18 hours after surgery.
13. Continually monitor drainage and elapsed time. Determine hourly drainage rate.
WARNING Reinfusion of collected blood/fluid should be done on an hourly basis unless fewer than 50 mL are collected hourly.
14. Upon collection of 50 mL of blood, remove the end cap of the blood infusion adapter line and attach the blood infusion adapter to an I.V. Administration set/pump apparatus.
NOTE: It is recommended that the infusion pump be used with an air detection sensor for all reinfusion procedures.
15. Unclamp the blood infusion line and proceed with autotransfusion.
WARNINGS
• To reduce risk of air embolism, evacuate all air completely from the infusion line prior to autotransfusion.
• To minimize blood damage, do not exceed 13.3-20 kPa (100-150 mmHg) (130-195 cmH
• The physician is responsible for determining the optimal time, rate and volume to be autotransfused to the patient.
• The clinician should be aware of potential complications such as air emboli, associated with the use of the I.V. Administration set and the infusion pump. Use the I.V.
Administration set and the infusion pump in accordance with the instructions provided by the manufacturers.
SPECIFICATIONS
Product Description
Reorder Number
CX*FX25RW
CX*FX25RE
CX*FX25W
CX*FX25E
(Refer to "DIRECTION OF BLOOD OUTLET PORT", page 5)
CAPIOX FX25 Oxygenator Module
COMPONENT
Housing Material
Fibers Material
Surface area
Arterial filter Material
Heat Exchanger Material
Surface area
Blood Flow Range
Priming Volume ( Static )
Blood inlet port ( from pump )
Blood outlet port
Cardioplegia port
Gas inlet port
Gas outlet port
Water ports
Maximum Pressure
14
Oxygenator with integrated arterial filter with Hardshell Reservoir
Oxygenator with integrated arterial filter with Hardshell Reservoir
Oxygenator with integrated arterial filter
Oxygenator with integrated arterial filter
SPECIFICATIONS
Polycarbonate
Microporous Polypropylene
Approx. 2.5 m
2
Polyester screen type
Pore size 32 μm
Stainless steel
Approx. 0.2 m
2
Min. 0.5 L/min Max. 7.0 L/min
260 mL
3/8" (9.5 mm)
3/8" (9.5 mm)
1/4" (6.4 mm)
1/4" (6.4 mm)
1/4" (6.4 mm)
1/2" (12.7 mm) Hansen quick connect
fittings
Blood inlet 133 kPa (1,000 mmHg)
Water inlet 196 kPa (2 kgf/cm )
2
O) pressure when reinfusing blood.
2
Description
Hardshell Reservoir Section
COMPONENT
Housing Material
Blood Flow Range
Blood Storage Capacity
Minimum Operating Volume
Venous Filter Material
Cardiotomy Filter Material
Defoaming Part Material
Venous blood inlet port
Blood outlet port ( to pump )
Suction ports
Vertical port to CR filter
Quick prime port
Vent port
Auxiliary port
Luer ports
Maximum Sustainable Negative Pressure
in Reservoir
SPECIFICATIONS
Polycarbonate
Venous Flow : Min. 0.5 L/min
Max. 7.0 L/min
Cardiotomy Inlet : Max. 5.0 L/min
Combined Flow : Max. 7.0 L/min
4,000 mL
200 mL
Polyester screen type
Pore size 47 μm
Polyester depth type
Polyurethane foam
1/2" (12.7 mm) rotatable
3/8" (9.5 mm)
six 1/4" (6.4 mm)
3/8" (9.5 mm)
1/4" (6.4 mm)
1/4" (6.4 mm)
1/4"—3/8" (6.4 mm—9.5 mm)
-three filtered luer locks to cardiotomy
filter
-a non-filtered luer lock
-two luer locks on venous inlet
-20 kPa (-150 mmHg)