Business Type:
Manufacturer/Factory,Trading Company
Business Range:
Syringe, Infusion Set, Hernia Mesh, Glove, Urine Bag, Scalp Vein Set
Establishment:
1988
R&D Capacity:
OwnBrand, ODM, OEM
Terms of Payment:
LC, T/T, D/P, PayPal, WesternUnion, Small-amountpayment
Main Markets:
North America, South America, Europe, Southeast Asia, Middle East, Africa, East Asia(Japan, South Korea), Australia, Domestic
OEM/ODM Service
Sample Available

Disposable Syringe 1ml-100ml, Medical Syringe, Medical Syringe with Needle manufacturer / supplier in China, offering Medical Disposable Injection Needle Syringe 1ml-100ml with Needle or Withou Needle with Ce and ISO Certification Manufacturer in China, Medical Disposable I. V. Cannula, Disposable 2-Parts Syringe with CE ISO13485 GMP and so on.

1
    YRS
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Supplier Homepage Health & Medicine Medical Supply Disposable Medical Supplies China Ce ISO Disposable Infusion Set with Y Set with 21g Needle

China Ce ISO Disposable Infusion Set with Y Set with 21g Needle

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Min. Order / Reference FOB Price
50000 Piece US $0.08/ Piece
Local Area: Jian, Jiangxi, China
R&D Capacity: OEM, ODM, Other
Payment Terms: LC, T/T, D/P, PayPal, WesternUnion, Small-amountpayment
Type: Infusion Set
Material: Plastic
Ethylene Oxide Sterilization: Ethylene Oxide Sterilization
Disposable infusion se with Y site with needle 21G
Disposable syringe with all Certification
Name of Parts Name & Code of Raw Materials
1. Cover Polypropylene P. P HT-022
2. Cannula Stainless Steel 1Cr18Ni9Ti
3. Hub Polypropylene P. P HT- 022
4. Plunger Polypropylene P. P HT-022
5. Barrel Polypropylene P. P HT-022
6. Piston Natural rubber for medical
7. Needle Stainless steel
B. Microbiologic, Chemical and Physical Properties
1. Microbiologic and Chemical properties
A. Sterility: Sterility
B. Pyonenicity: Non-pyroenicity
C. Limit for extractable metal: For the metals content of the control fluid, contain not greater than a combined total of 5mg/l of lead, tin, zinc and iron. The cadmium content of the extract shall, when corrected for the cadmium content of the control fluid, be lower than 0.1mg/l
D. Titration acidity: When determinded with a laboratory PH meter and using a general purpose electrode, the PH value of an extract prepared in accordance with annex A shall be within one unit of PH of that of the control fluid evaporation.
2. Physical Property
A. Cleanliness
When inspected by normal or corrected-to-noumal visio without magnification
Under an luminance of 300ix to 700ix, the surface of the hypodermic syringe which comes in contact with injection fluids during normal use shall be free from particles and extraneous matter.
B. Lubricant
An acceptable lubricant, applied undiluted, for three-piece syringes is polydimethylsiloxane complying with a national or the European Pharmacopoeia. The quantity of lubricant used should be exceed 0.25mg per square centimeter of the internal surface area of the syringe barrel.
C. Tolerance on graduated capacity
The tolerance on the graduated capacity shall be as table 1 of ISO7886-1: 1993
D. Graduated scale
The graduated scale should be as 10 of ISO7886-1: 1993.
E. Barrel
Dimensions should be accordance with 11.1 of ISO7886-1: 1993
Finger grips should be accordance with 11.2 of ISO7886-1: 1993
F. Piston/plunger assembly
Design should be accordance with 12.1 of ISO7886-1: 1993
Fit of piston in barrel should be 12.2 of ISO7886-1: 1993
Fiducial line should be accordance with 12.3 of ISO7886-1: 1993
G. Nozzle
Conical fitting should be accordance with 13.1 of ISO7886-1: 1993
Position of nozzle on end of barrel should be accordance with 13.2 of ISO7886-1: 1993
Nozzle lumen should be accordance with 13.3 of ISO7886-1: 1993
H. Performance
Dead space should be accordance with 14.1 of ISO7886-1: 1993