Gold Member Since 2007
Audited Supplier
Changzhou Yuandong Medical Equipments Co., Ltd.

Infusion Set, Disposable Infusion Set, Plastic Infusion Set manufacturer / supplier in China, offering Disposable Steriled Infusion Sets with CE &ISO Approvaled, Flock Line Latex /Rubber Household Gloves, Disposable Medcial Use Vinyl Gloves, PVC Gloves and so on.

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Supplier Homepage Product Disposable syringe /Infusion set/Needle Disposable Steriled Infusion Sets with CE &ISO Approvaled

Disposable Steriled Infusion Sets with CE &ISO Approvaled

FOB Price: Get Latest Price
Min. Order: 300,000 Pieces
Port: Shanghai, China
Production Capacity: 300, 000PC Per Day
Payment Terms: L/C, T/T, D/P, Western Union

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Basic Info
  • Model NO.: NEO -105
  • Material: Plastic
  • Ethylene Oxide Sterilization: Without Ethylene Oxide Sterilization
  • Group: Adult
  • Medical Device Regulatory Type: Type 3
  • Trademark: IU
  • Specification: CE certificate and ISO
  • HS Code: 90183900
  • Type: Infusion Set
  • Certification: CE, FDA, ISO13485
  • Quality Guarantee Period: 5 Year
  • Logo Printing: With Logo Printing
  • Medical Devices Reg./Record No.: Ssyjxzz-2001-0249
  • Transport Package: 1PC Per Bag, 500PS Per CTN, 800CTN /40hq Container
  • Origin: Jiangsu, China
Product Description
Disposable steriled  Infusion Sets with CE &ISO approvaled  with 21G injection needle 

Consist of:

1) Sterilized by EO gas, the product is non pyrogen and non-toxic 
2) Material: Polypropylene 
3) Application: Used for body vein infusion 
4) Big ABS spike and molding plastic drip 
5) Thick latex tube 
6) luer lock for connecting needles 
7) Custom specifications welcomed for completion 

Inner packing: 
Individual polybag or individual polybag with dialyzer or individual blister bag 

1. CE and ISO certificate 
2. Stable quality and strict quality control 
3. Great production capacity 
4. Favourable price

Remark: You can also give us your specific requirements to confirm the products you need finally.

Disposable Steriled Infusion Sets with CE &ISO Approvaled
Disposable Steriled Infusion Sets with CE &ISO ApprovaledDisposable Steriled Infusion Sets with CE &ISO Approvaled
Name of SampleDisposable Infusion Set with needleTypeIS-VZ  0.7
LOT NO 20130618Testing Standardscontract requirements
Sterilization Lot20130618Quantity of Tested Batch1260000 pcs
Quantity Of Sample50pcsTesting DateSEP 7, 2013
TypeTesting itemsStandard Requirement and Standard Term and ConditionsActual Testing ResultConclusion
Biological Properties Sterility The infusion set in individual package should be sterile (8.2) Missing/
Pyrogen Infusion set has no pyrogen (8.3) Missing/
Chemical Properties 
Reduction MatterDifference of volumes of potassium permanganate [ c(kmno4 = 0.002mol/L)] consumed by test liquid and blank liquid should be not more than 2.0 ml (7.1)0.5mlEligible
PhThe PH difference between testing liquid and blank liquid is not more than 1.5 (7.3)0.19Eligible
Ultraviolet Absorbance The absorbance of testing liquid should be not more than 0.1 (7.5)0.046Eligible
Ethylene Oxide Residuum The ethylene oxide residuum should be not more than0.5mg; Unit: mg  (7.6)   0.29/
Physical Properties
Particle Content For the number of 15-25min particles in 200ml eluent, not more than 1 particle/mlEligibleEligible
For the number over 25min particles, not more than 0.5 particle/ml (6.1)Eligible
Sealing PropertyNo air leakage of infusion set (6.2)EligibleEligible
Connection IntensityConnection of parts for liquid channel of infusion set can bear the static tensile force not less than 15N for 15 seconds. (6.3) EligibleEligible
Puncture Device Of Bottle StopperAccording to the contract requirements
,Materials for ABS.
Liquid Medicine FitterThe infusion set should be equipped with a liquid machine filterEligibleEligible
The filtering rate of liquid medicine should be not less than 80%. (6.7)98.7%
Flow Speed Of Transfusion (Flow Quantity)For the infusion set with 20drops/ml, with 1m static press end, the sodium chloride solution flowed should be not less than 1000ml for 10 minutes
Unit: ml  (6.10)
Air Inlet Device (Air Fitter)The filtering rate against particles 0.5μm in air should be not less than 90%. (6.5.2)Missing/
Air Inlet Device (Flow Reduction Rate )Comparing with vessel with free air input, the flow of effluent should be reduced by 20%. (6.5.5)EligibleEligible
Packaging requirementsAccording to the contract requirementsEligibleEligible
Flow AdjustorMaterials for ABS.EligibleEligible
Soft Pipe (Length)According to the contract requirementsEligibleEligible
needleAccording to the contract requirementsEligibleEligible
Testing ResultsThe seized products meet the requirements of 
the  contract .
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