Pediatric Disposable Infusion Set 100ml 150ml Medical Disposable Burette Infusion Set
Medical disposable pediatric burette infusion set
Components:Disposable burette-type infusion set is made up of protective cap, closure-piercing device, drip chamber, tubing, flow regulator, fluid filter, air filter, injection site, 15.3x54MM drip chamber, 60drop/ml, hypodermic needle or intravenous needle and other accessories.
List of main raw materials for burette-type infusion sets:
- Medical grade PP, PE, ABS
- Medical grade PVC for burette-type infusion sets
- Colorant for burette-type burette-type infusion set molding
- Injection site for adding medicine
- Hypodermic needle and intravenous needle for burette-type infusion set
- PE individual package of burette-type infusion set
- Dialyzing paper for blister package of burette-type infusion set
- Plastic film for individual package of burette-type infusion set
- PE medium packing bag for burette-type infusion set
- White board box for burette-type infusion set inner packing
- Corrugated carton for burette-type infusion set outer packing
Intended Use of the Product:
- The disaposible burette-type infusion set is maily applied to clinical intravenous infusion in medical institutions.
- The disaposible burette-type infusion set should be nonpoisonous, sterile, non-pyrogen and no subcutaneous stimulation after sterilized by ethylene oxide gas. The hemolysis rate should be less than 5%, and the leftover of ethylene oxide gas should be no more than 0.5mg per piece.
Features of burette infusion set:
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Biological Performance |
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Sterilization |
EO gas sterilization |
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Pyrogen |
Pyrogen-free |
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Chemical Performance |
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Reducing Material |
0.005mol/L Sodium thiosulfate Consumption Difference ≤2.0mL |
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Titration acidity or alkalinity |
Volume of required sodium hydroxide standard solution or hydrochloric acid standard solution≤1ml |
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Ultraviolet Absorption |
≤0.1 |
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Residue on Evaporation |
The total amount of dry residue shall not exceed 5 mg |
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EO Remnants |
No more than 0.5mg for each set |
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Physical Performance |
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Particulate contamination |
Contamination index limit N≤90 |
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Leakage test |
Immerse the set with one end blocked in water at (40±1)℃ and apply pressure of 20KPa for 15s; fill the set with degassed, distilled water, subject it to an internal excess pressure of -20KPa at (40±1)℃ for 15s, air leakage shall not be observed. |
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Tensile strength |
Connection between components, protective jacket excluded, should be able to withstand a static force of not less than 15N for 15s. |
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Closure-piercing device |
Pierce and penetrate closure of a fluid container without pre-piercing, no coring should occur. |
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Air Filter |
Air filter rate ≥90%,Flow reduction by air filter<20% |
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Soft Tube |
Tube should be transparent or sufficiently translucent, when bubbles pass by, normal or corrected eyesight is able to observe air and water interface. |
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Liquid Filter Rate |
Liquid filter rate≥80% |
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Volume Tolerance |
Tolerance on capacity greater than half of nominal capacity should be ± 4% of expelled volume. |
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Flow Regulator |
Flow regulator can be used without damaging the tube during an infusion, and no deleterious reactions occur when stored with tube. |
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Flow Rate |
Under 1m static head, for 20 drops/ml drip chamber, the infusion set shall deliver not less than 1000ml of sodium chloride solution (ρ=9g/L) within 10min; for 60 drops/ml drip chamber, the infusion set shall deliver not less than 1000ml of sodium chloride solution within 40min. |
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