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Pediatric Disposable Infusion Set 100ml 150ml Medical Disposable Burette Infusion Set

Yangzhou Easier Way Import and Export Co., Ltd.

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Pediatric Disposable Infusion Set 100ml 150ml Medical Disposable Burette Infusion Set

Country/Region china
City & Province jiangsu
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Product Details

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:

  1.  Medical grade PP, PE, ABS
  2.  Medical grade PVC for burette-type infusion sets
  3.  Colorant for burette-type burette-type infusion set molding
  4.  Injection site for adding medicine
  5.  Hypodermic needle and intravenous needle for burette-type infusion set
  6.  PE individual package of burette-type infusion set
  7.  Dialyzing paper for blister package of burette-type infusion set
  8.  Plastic film for individual package of burette-type infusion set
  9.  PE medium packing bag for burette-type infusion set
  10.  White board box for burette-type infusion set inner packing
  11.  Corrugated carton for burette-type infusion set outer packing

Intended Use of the Product:

  1.  The disaposible burette-type infusion set is maily applied to clinical intravenous infusion in medical institutions.
  2.  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:

 

Biological Performance

Sterilization

EO gas sterilization

Pyrogen

Pyrogen-free

Chemical Performance

Reducing Material

0.005mol/L Sodium thiosulfate Consumption Difference ≤2.0mL

Titration acidity or alkalinity

Volume of required sodium hydroxide standard solution or hydrochloric acid standard solution≤1ml

Ultraviolet Absorption

≤0.1

Residue on Evaporation

The total amount of dry residue shall not exceed 5 mg

EO Remnants

No more than 0.5mg for each set

Physical Performance

Particulate contamination

Contamination index limit N≤90

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.

Tensile strength

Connection between components, protective jacket excluded, should be able to withstand a static force of not less than 15N for 15s.

Closure-piercing device

Pierce and penetrate closure of a fluid container without pre-piercing, no coring should occur.

Air Filter

Air filter rate ≥90%,Flow reduction by air filter<20%

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.

Liquid Filter Rate

Liquid filter rate≥80%

Volume Tolerance

Tolerance on capacity greater than half of nominal capacity should be ± 4% of expelled volume.

Flow Regulator

Flow regulator can be used without damaging the tube during an infusion, and no deleterious reactions occur when stored with tube.

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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