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Innovation Biotech (Beijing) Co., Ltd.

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City:beijing

Province/State:beijing

Contact Person:MissRebecca

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China FDA CE Approved Covid 19 Rapid Test Card IgG IgM Antibody Home Kit wholesale

FDA CE Approved Covid 19 Rapid Test Card IgG IgM Antibody Home Kit

Name: FDA CE Approved Covid 19 Rapid Test Card IgG IgM Antibody Home Kit
Brand: INVBIO
Price: 0.55 USD

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Brand Name :INVBIO

Model Number :INVBIO-Covid Ab

Certification :CE, FSC

Place of Origin :China

MOQ :1000pcs

Price :usd0.55-1.5/pcs

Payment Terms :T/T, Western Union

Supply Ability :1million per day

Delivery Time :3-5 days after receiving payment

Packaging Details :25pcs/box; 5pcs/box; 1pcs/box

Format :Card

Sensitivity :87.8%

Accuracy :>96.8%

Specificity :99%

Specimen :serum, plasma, or whole blood

Packing :25pcs/box; 1pcs/box

Shelf life :2years

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FDA CE Approved Covid 19 Rapid Test Card IgG IgM Antibody Home Kit

Product Description

The Coronavirus COVID-19 IgG/IgM Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of IgG&IgM antibody of Coronavirus Disease 2019 in human whole blood,serum,or plasma as an aid in the diagnosis of COVID-19 infections.

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Date sheet

Product name:	Covid -19 Antibody igg igm rapid test kit
Format:	Card
Specimen:	serum, plasma, or whole blood
Sensitivity:	87.8%
Accuracy:	96.8%
Specificity:	99%
Packing	25pcs/box; 1pcs/box
shelf life	2years
Certificate:	CE , FSC,FDA

Directions for Use

1. The serum, plasma or whole blood specimen should be collected under standard laboratory conditions.

2. Heat inactivation of specimens, which may cause hemolysis and protein denaturation, should be avoided.

3. The test works best on fresh whole blood / serum / plasma samples. If testing cannot be performedimmediately, serum / plasma may be stored at 2-8ºC up to 3 days in case of delay in testing. For long-term storage, serum / plasma specimens can be frozen at -20ºC for 3 months or -70ºC for longer period. Avoid

repeated freezing/thawing cycles.

4. Sodium azide can be added as a preservative up to 0.1% without affecting the test results

PROCEDURE

1,Bring the kit components to room temperature before testing.

2,Open the pouch and remove the Card. Once opened, the test card must be used immediately.

3,Label the test card with patient identity.

4.Withdraw the blood specimen with the capillary pipet provided, gently squeeze out the extra specimen to leave 2 μL in the pipet as marked with the scale line. Apply 2 μL of blood specimen to the “S1” area as marked.

5.Add 2 drops of sample buffer(approximately 80-100 μL) to well marked as “S”.

6.Read the result at 15 minutes. A strong positive sample may show result earlier.

Note: Results after 20 minutes may not be accurate

Read result:

IgG POSITIVE:*

The colored line in the control line region (C)appears and a colored line appears in test line region IgG. The result is positive forCOVID-19-IgG antibodies.

IgM POSITIVE:*

The colored line in the control line region (C)appears and a colored line appears in test line region IgM. The result is positive for COVID-19-IgM antibodies and is

indicative of primary COVID-19 infection.

IgG AND IgM POSITIVE:*

The colored line appears in the control line region (C) and two test line regions antibodies. (IgG a d IgM). The result is positive for COVID-19-IgG and COVID-19-IgM

NOTE: The intensity of the color in the test line region(s) IgG and/or IgM may vary depending on the concentration of COVID-19 antibodies in the specimen. Therefore, any shade of color in the test line region(s) IgG and/or IgM should be considered positive.

NEGATIVE: The color line region IgG or IgM. red line in the control line region (C) appears. No line appears in test

INVALID: There is no line appeared in the C region.

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

Company Information

Innovation Biotech (Beijing) Co., Ltd. is a biotechnology company specializing in research, development and manufacturing of advanced medical in-vitro diagnostic (IVD) rapid test kits, medical and laboratory disposal products. We provide one step medical diagnostic rapid test kit based on our INVBIO brand, Product include Fertility Tests, Tumor markers, DOA drug of abuse test, Drug test cup, Urinalysis reagent strip, ELISA kit, Digital alcohol tester, urine analyzer, et.

OEM packaging is available, drug of abuse test, troponin I test, alcohol screening saliva test strips, urine strips, elisa kits, microscope slides

Our focus is to expand our markets internationally by forming strategic alliances and entering into partnerships with distributors worldwide. We have established an international reputation for excellence in the manufacturing of quality medical and laboratory products. In addition, we have obtained approval licenses ISO13485, FSC certificate, and most of our products get CE mark Our objective is the utmost satisfaction of our clients all around the world by supplying our quality and economical products

Certifications

FAQ

Q: What is your payment terms?

A: Payment terms: 100% TT before shipment

Q: Can you send samples?

A: Yes,SAMPLES can be sent for your evaluation.customer pay the freight charge

Q: Do you give any discount?
A: I'll surely try my best to help you get those by the best price and good service at the same time. We promise the best price upon same quality, and best quality upon same price.
Q: How to order?
A: Please tell us the model and quantity and package requests.
b. Proforma Invoice confirmed, the order will be arranged upon receipt of your payment.
c. Confirm and ship the goods.
d. We will help to track your goods until you receive them safely.

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