PriceList for Chemiluminescence Immunoassay - C-creactive protein CRP rapid test kit – Baysen factory and manufacturers

PriceList for Chemiluminescence Immunoassay - C-creactive protein CRP rapid test kit – Baysen

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Our purpose would be to offer good quality products at competitive price ranges, and top-notch support to clients around the whole world. We're ISO9001, CE, and GS certified and strictly adhere to their good quality specifications for E2 Test Kit , Fsh Diagnostic Kit , Hepatitis C Diagnostic Kit , We attend seriously to produce and behave with integrity, and by the favor of customers at home and abroad in the xxx industry.

PriceList for Chemiluminescence Immunoassay - C-creactive protein CRP rapid test kit – Baysen Detail:

Diagnostic Kit for C-reactive Protein

Methodology:Fluorescence Immunochromatographic Assay

Production information

Model Number	CRP	Packing	25 Tests/ kit, 30kits/CTN
Name	Diagnostic Kit for C-reactive Protein	Instrument classification	Class I
Features	High sensitivity, Easy opeation	Certificate	CE/ ISO13485
Accuracy	> 99%	Shelf life	Two Years
Methodology	Fluorescence Immunochromatographic Assay	OEM/ODM service	Avaliable

INTENDED USE

This kit is applicable to the vitro quantitative detection of C-reactive protein (CRP) in human serum/plasma/whole blood samples, for auxiliary diagnosis of acute and chronic inflammation or infection. This kit only provides the test result of C-reactive protein, and the obtained result shall be analyzed in combination with other clinical information.

Test procedure

1	Before using the reagent,read the package insert carefully and familiarize yourself with the operating procedures.
2	Select standard test mode of WIZ-A101 portable immune analyzer
3	Open the aluminum foil bag package of reagent and take out the test device.
4	Horizontally insert the test device into the slot of immune analyzer.
5	On home page of operation interface of immune analyzer, click “Standard” to enter test interface.
6	Click “QC Scan” to scan the QR code on inner side of the kit; input kit related parameters into instrument and select sample type. Note: Each batch number of the kit shall be scanned for one time. If the batch number has been scanned, then skip this step.
7	Check the consistency of “Product Name”, “Batch Number” etc. on test interface with information on the kit label.
8	Take out sample diluent upon consistent information, add 10μL serum/plasma/whole blood sample, and thoroughly mix them;
9	Add 80µL aforesaid thoroughly mixed solution into well of test device;
10	After complete sample addition, click “Timing” and remaining test time will be automatically displayed on the interface.
11	Immune analyzer will automatically complete test and analysis when test time is reached.
12	After test by immune analyzer is completed, test result will be displayed on test interface or can be viewedthrough “History” on home page of operation interface.

Note: each sample shall be pipetted by clean disposable pipette to avoid cross contamination.

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