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China factory - Orient New Life Medical Co.,Ltd.

Orient New Life Medical Co.,Ltd.

  • China,Ningbo ,Zhejiang
  • Active Member

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China High Sensitivity CEA Blood Test Cassette Monitoring Cancer Patients For
China High Sensitivity CEA Blood Test Cassette Monitoring Cancer Patients For

  1. China High Sensitivity CEA Blood Test Cassette Monitoring Cancer Patients For
  2. China High Sensitivity CEA Blood Test Cassette Monitoring Cancer Patients For

High Sensitivity CEA Blood Test Cassette Monitoring Cancer Patients For

  1. MOQ: 5000pcs
  2. Price: USD0.5-USD2
  3. Get Latest Price
Payment Terms T/T, Western Union
Supply Ability 2000000pcs/month
Delivery Time 20-30days
Packaging Details 1pc/pouch, 25pcs/box
Category Tumor mark test
Format Strip/cassette
Specimen Whole Blood/Serum/Plasma
Testing time 5-15 minutes
Shelf Life 24 Months
Application Carcinoembryonic Antigen
Accuracy 99.46%
Brand Name New Life
Model Number Cassette
Certification ISO13485,CE
Place of Origin China

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  1. Product Details
  2. Company Details

Product Specification

Payment Terms T/T, Western Union Supply Ability 2000000pcs/month
Delivery Time 20-30days Packaging Details 1pc/pouch, 25pcs/box
Category Tumor mark test Format Strip/cassette
Specimen Whole Blood/Serum/Plasma Testing time 5-15 minutes
Shelf Life 24 Months Application Carcinoembryonic Antigen
Accuracy 99.46% Brand Name New Life
Model Number Cassette Certification ISO13485,CE
Place of Origin China
High Light cancer test kitcancer marker test

High Accuracy Tumor Mark CEA Rapid cassette, for detecting Carcinoembryonic Antigen in serum, gold colloidal method

 

Product Name: CEA Rapid Diagnostic Test

 

 

Intended Use:

 

 

 

The CEA Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of CEA in whole blood, serum or plasma to aid in monitoring of cancer patients.

 

Test Principle:

 

The CEA Rapid Test Cassette (Whole Blood/Serum/Plasma) is a qualitative membrane based immunoassay for the detection of CEA in whole blood, serum or plasma. The membrane is pre-coated with anti-CEA antibodies on the test line region. During testing, the specimen reacts with the particle coated with anti-CEA antibodies. The mixture migrates upward on the membrane chromatographically by capillary action to react with anti-CEA antibodies on the membrane and generate a colored line. The presence of this colored line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear in the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.

 

 

TEST PROCEDURE

 

1. Bring the pouched test device to room temperature(15-30℃) prior to testing. Do not open the pouch until ready to begin testing.

 

2. Remove the device from the sealed pouch and lay it on a flat and dry surface.

 

3. Using the provided pipette, add one drop of fresh specimen to the sample well.

 

4. Hold the buffer bottle vertically and add 1 drop to the sample well. /If using a pipette, change a new one to avoid cross-contamination. Draw and transfer 2-3 drops of buffer to the sample well.

 

5. Read the result between 15-20minutes. Do not read results after 20 minutes.

 

INTERPRETATION OF RESULTS

 

POSITIVE:* Two lines appear. One colored line should be in the control line region (C) and another apparent colored line should be in the test line region (T).

 

*NOTE: The intensity of the color in the test line region (T) will vary depending on the concentration of TP antibodies present in the specimen. Therefore, any shade of color in the test line region (T) should be considered positive.

 

NEGATIVE: One colored line appears in the control line region (C). No line appears in the test line region (T).

 

INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

 

PERFORMANCE CHARACTERS:

 

 

Sensitivity and Specificity

 

The CEA Rapid Test Cassette (Whole Blood/Serum/Plasma) has correctly identified a panel of specimens and has been compared to a leading commercial CEA EIA test using clinical specimens. The results show that the relative sensitivity of the CEA Rapid Test Cassette (Whole Blood/Serum/Plasma) is 98.9%, and the relative specificity is 99.5%.

 

Method EIA Total Results

CEA Rapid

Test Cassette

Results Positive Negative
Positive 188 2 190
Negative 2 400 402
Total Results 190 402 592

 

Relative Sensitivity: 98.9% (95%CI*: 96.2%-99.9%) * Confidence Interval

 

Relative Specificity: 99.5% (95%CI*: 98.2%-99.9%)

 

Accuracy: 99.3% (95%CI*: 98.3%-99.8%)

 

 

 

 
ORIENT NEW LIFE MEDICAL CO., LTD.
Contact: Jerry Meng
Email: Jerry @ newlifebiotest .com
Tel. +86 18657312116
SKYPE enetjerry

Company Details

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 from Quality China Factory
  • Business Type:

    Manufacturer,Exporter

  • Year Established:

    2009

  • Total Annual:

    10,000,000-15,000,000

  • Employee Number:

    200~300

  • Ecer Certification:

    Active Member

Established in 2009, Orient New Life Medical Co., Ltd., is specialized in high-tech biological diagnostic test development, research and production, as well as high-tech medical device development, research and production. New Life has built up two production base, which produce biological diagnosti... Established in 2009, Orient New Life Medical Co., Ltd., is specialized in high-tech biological diagnostic test development, research and production, as well as high-tech medical device development, research and production. New Life has built up two production base, which produce biological diagnosti...

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  • Orient New Life Medical Co.,Ltd.
  • 12F,Guting Building,Hefeng Creative Square,No.495 Jiangdong North Road,Ningbo,Zhejiang, China
  • https://www.medicaldiagnostictestkits.com/

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