Model NO.: CY-YDS005-4
Logo Printing: as Per Customers′ Requests
Trademark: CIYE
Transport Package: Carton
Specification: 150ml-2000ml
Origin: China
HS Code: 3926909090
Medical Disposable PVC Blood Bag 
 
Blood bags are widely used in the hospitals and blood banks for the safe storage of blood in the world. 
It adopts high grade medical PVC made in or . They're accessible with integrated donor tubing at regular intervals for easy cross matching, processing and identification.

Features: 
1) Anticoagulants: CPDA-1; SAGM
2) Single: 100ml - 500ml
3) Double: 100ml - 500ml
4) Triple: 100ml - 500ml
5) Quadruple: 100ml - 500ml
6) Single package OPP compound film bag, in lightproof aluminum foil

1. Blood bag types available: CPDA -1 / CPD / SAGM. 
2. With Safety Needle Shield. 
3. With Sampling bag and Vacuum Blood Collection Tube Holder. 
4. High quality film suitable for extended storage of viable platelets for approximately 5 days. 
5. Blood bag with leikoreduction filter. 
6. Transfer empty bag is also available from 150ml to 2000ml for separating blood components from whole blood.

Specifications
Single: 100ml - 500ml
Double 100ml - 500ml
Triple 100ml - 500ml
Quadruple 100ml - 500ml

Snap-tip system In quadruple bags, a simple bend of the connection tube allows blood components to be transferred into integral satellite bags.  

Packing: All bags are individually packed and sealed. Each bag remains sterile even despite of  the outer aluminum foil package or plastic package.
    3--5 units of blood bags be packaged in an aluminum pouch.
    45---80 units of blood bag be packaged in a master carton

Please contact  us for more details.

 
Medical Disposable PVC Blood Bag
 

ELISA Analyzer

Processing high-throughput samples, intelligent reuse for large-capacity publishing, work surface: 200cm, 8 sample injection needles, 12 temperature-controlled incubation positions, 12 room temperature incubation positions, 32 plate storage positions, Sunrise microplate reader, HydroFlex plate washer, up to 512 specimens, sequential loading of samples, reagents, microplates Parallel loading of up to 6 plates for fast dispensing.

The automatic enzyme immunoassay analyzer is based on the principle that the enzyme and the substrate can produce a color reaction, the absorption lines of different substances have different characteristics, and strictly abide by the Lambert-Beer law, quantitative and qualitative analysis of substances. instrument. The method of analyzing the content of various enzymes such as antigen or antibody generally mainly adopts colorimetric method. In practice, spectrophotometry is the basic working principle of an automatic enzyme immunoassay analyzer. The light emitted by the light source lamp becomes a beam of monochromatic light after passing through a filter or a monochromator. The monochromatic light beam passes through the sample to be tested in the microtiter plate, and part of the monochromatic light beam is absorbed by the sample and reaches the photodetector. The intensity of the light signal projected on it is converted into the magnitude of the electrical signal by the photodetector. This electrical signal is processed by pre-amplification, logarithmic amplification, analog-to-digital conversion, etc., and then sent to the microprocessor for data processing and calculation, and the test results are output by the display and printer. The microprocessor completes the movement in the X and Y directions of the mechanical drive through the control circuit.
The automatic enzyme immunoassay analyzer adds the sample to the microwells of the pre-coated antigen or antibody microtiter plate, washes after the reaction, removes the unseparated ligand, then adds the enzyme isolate, after incubation, washes again , remove the unseparated compound, and then add the enzyme substrate, after the reaction, the colored final product is formed, and the stop solution is added to stop the reaction. The absorbance of each microwell of the microtiter plate is read by the wavelength that has been set by the spectrophotometer. The concentration value of the analyte in the sample is calculated by the absorbance value of the sample and the standard curve, so that the quantitative result can be obtained, or the absorbance of the sample is compared with that of the standard product, so that the positive or negative qualitative result can be obtained.

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Jilin Sinoscience Technology Co. LTD , https://www.jlgkscience.com