Medical Diagnostic Zika Virus Igg/Igm Antibody Rapid Test

• Customization: Available
• Classification: Biological Diagnostics
• Type: Ivd Rapid Test Kits
• Model NO.: 101048
• Certification: CE, MSDS, ISO13485
• Group: Adult
• Package: 40PCS/Box or 25PCS/Box
• Certificate: ISO 13485 / CE / ISO 9001
• Specimen: Wb/S/P
• Shelf Life: 24 Months
• Storage: 4-30°c
• Format: Cassette
• OEM: Available
• Procedure: Simple
• MOQ: 500PCS
• Application: Infectious Diease Test
• Product name: Zika Virus Igg/Igm Antibody Test
• Transport Package: Carton
• Specification: 66*36*56.5cm
• Trademark: Testsealabs
• Origin: China
• Production Capacity: 1000000PC Per Day

Product Description

Testsealabs Zika virus IgG/IgM Antibody Rapid test

Product Description

 

Product name	Zika Virus Igg/Igm Antibody Test
Specimen	WB/S/P
Shelf Life	24 Months
Certificate	ISO 13485 / CE / ISO 9001
MOQ	500PCS

Intended Use
Zika Virus Antibody IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibody (IgG and IgM) to Zika virus in whole blood/serum/plasma to aid in the diagnosis of Zika viral infection.

Test Procedure:
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30ºC (59-86ºF) prior to testing.
 

1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
2. Place the test device on a clean and level surface.
3. Hold the dropper vertically and transfer 1 drop of specimen (approximately 10μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer. See illustration below.
4. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Notes:
Applying sufficient amount of specimen is essential for a valid test result. If migration (the wetting of membrane) is not observed in the test window after one minute, add one more drop of buffer   to the specimen well.

Interpretation of Results

Positive:Two lines appear. One line should always appear in the control line region(C), and another one apparent colored line should appear in the test line region.
Negative: One colored line appears in the control region(C).No apparent colored line appear in the test line region.
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 device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.





FAQs:
Q: What are your price?
A: Our price are subject to change depending on supply and other market factors. We will send you an updated price list after your company contact       us for further information.

Q: Do you have a minimum order quantity?
A : Yes, require all international orders to have an ongoing minimum order quantity. If you are looking to resell but in much smaller quantities, we recommend you check our our website.

Q: Can you supply the relevant documentation?
A: Yes, we can provide most documentation including certificates and other export documents where required.

Q: Can you make OEM or ODM service?
A: Yes. We can accept OEM service. Meanwhile it's also welcome to choose our ODM products.