Find Verified Igg Igm Co 19 Test Suppliers, Manufacturers and Wholesalers

COVID-19 rapid test kit designed for qualitative detection according to the manufacturer's intended use and instructions. The kit is supplied in sealed packaging and may include a test device, extraction components, a sterile swab, and an instruction manual. Suitable for institutional procurement, healthcare distribution channels, and authorized markets where regulatory requirements are met.

Important: Product claims, intended use, certifications, and regulatory approvals must match the actual manufacturer documentation before publishing.

Our Covid-19 rapid test kits are a serology test using a novel way to identify to identify exposure to the Covid-19 virus by the identification of the IgM/IgG antibodies through a sample of serum, plasma
or whole blood. The presence of the antibodies is revealed in 15 minutes and does not require any specialised laboratory equipment for the execution of the test.

Test kits are packaged with 25 sealed pouches holding the test cassettes, an instruction set, 25 capillary tubes for making 25 tests and a bottle of 3ml with buffer solution to execute 25 tests. The test pouch contains the test cassette and a sterilizer pad to be used to disinfect the fingertip in case of fingerprint blood sampling.

(A) Name of product: COVID-19 IgM/IgG Antibody Rapid Test

(B) Price $4 EXW

(c) Origin: Canada

(d) Features:
Artron COVID-19 IgM/IgG Antibody Test is a rapid, qualitative, and convenient immunochromatographic in vitro assay for the differential detection of IgM &/or IgG antibodies to SARS-COV-2 in human serum, plasma or whole blood samples. The device is designed to aid in the determination of recent or previous exposure to SARS-COV-2 virus tracking the bodyâ??s immunity status to the virus after SARS-COV-2 infection.

(E) HS code:382200

(F) 20,000 units

(g) Carton Size (LxWxH cm) 59*41*37 - 2,200 test per carton. 17.6kg.
25,000 kits per pallet.

COVID-19 IgM/IgG test kit (Colloidal Gold)

This kit is used for the qualitative determination of COVID-19 IgM/IgG antibodies in human serum, plasma and venous whole blood samples in vitro. as an auxiliary diagnosis of COVID-19 infection.

[Detection principle]
This kit uses colloidal gold immunochromatography. Testing COVID-19 IgG antibody and COVID-19 IgM antibody in human serum, plasma and whole blood samples. The blood samples diluent containing COVID-19 IgG antibody and/or COVID-19 IgM antibody chromatography to colloidal gold binding pad, recombinant with colloidal gold marked COVID-19 antigen antibody, forming colloidal gold - antigen complex, chromatography to test area, combining to precoated anti-human IgG antibody and/or anti-human IgM antibody respectively, forming complexes in the test area and presenting red precipitation line. Unbound rabbit IgG colloidal gold bond chromatography to quality control line (C) combined with precoated sheep anti-rabbit IgG antibody presented a red precipitation line.

If the samples do not contain COVID-19 IgG antibody and/or COVID-19 IgM antibody, there is no corresponding red precipitation line existed in the test area. A red precipitation line appears on the quality control line (C) no matter if there is COVID-19 IgG antibody and/or COVID-19 IgM antibody in the sample or not.

[Storage and Stablity]
1. Store at 2ï½?30â?? for 18 months in a cool place, no direct sunlight and no freeze preservation. The test card and sample diluent should be used up in 1 hour after opening the package (opening temperature 10~30â??, humidity 25%~95%).
2. The date of production and the term of use are labeled.

COVID-19 Rapid Test Kit IgG + IgM (Colloidal Gold) comes in packs of 40 tests and contains:
GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request.

To get over COVID-19 pandemic, especially the recent Omicron breakout, currently we are doing big promotions for three kinds of COVID-19 Ag kit. All are in stock and available right away.
1. Nasopharyngeal
2. Nasal
3. Saliva

Price and Minumum Quantity
Price FOB in USD: negotiable 0.8 to 1.8Minimum Order Qty: None Pieces
Production Capacity: 3,000,000/monthPackaging: 20 Tests/kit, 30 Kits/box, 12 Boxes/pallet
Sample: Available. Sample Cost Born By Supplier
Product Model And Origin
Brand: GENEDIAModel: 643G-S (Saliva)
Seller Code: Genedia w covid 19 agHS Code: 3002.15
Standards: Ce
Competitive Advantages
Allow wider testing with fast test time (10 minutes)
All necessary materials provided / no equipment needed
Sensitivity: 93.33%, specificity: 100%
Free sample. no moq. price is negotiable. customized packing.
Other Details
20 tests / kit
24 months from the date of manufacture
2 ~ 30c(35.6 ~ 86f) available for room temperature deliver
In stock. fast delivery.
1 x Instructions for Use Manual
40 x Test Cassettes
1 x Buffer
40 x Dropper

I am the manufacturer of COVID-19 RAPID TEST in China. The ACtest COVID-19 IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-nCoV-19 virus in human whole blood, serum or plasma. It is intended to be used by the professionals as a screening test and as an aid in the diagnosis of infection with nCoV-19 viruses. The product has obtained the CE certification and is on the list of government export permits. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries.

Product Description
COVID-19 Ab Test - Boditech

Price of product ( USD price or FOB price) :
USD6.5/test
FOB Korea

Product origin :
Republic Of Korea

HS code
3822.00.1020

Key Specifications/Special Features :
* Easy to use with small device
* Fast and precise result (10mins)
* Room temperatue storage
* Anti-viral IgG / IgM test
* Automated (AFIAS) or manual (iChroma II) platform
* Assay type: TRFLFA*, IgM/IgG
* Sample type: Whole blood / serum / plasma
* Sample prep / extraction: Fingertip blood(C-tip)/ tube blood

Certificates
FDA, CE, ISO13485, FSC - MFDS
* MFDS: Ministry of Food and Drug Safety of Korea

Minimum Order Size and Packaging details :
* MOQ: 1,000 tests
* Packing:
24kits/box (AFIAS-1/6)
25kits/box (ichroma II)

The Herpes Simplex Virus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of IgG antibodies to Herpes Simplex Virus (HSV) in human serum/plasma samples.

HSV-1 is usually associated with infection in oropharyngeal area and eyes, while HSV-2 causes mostly genital and neonatal infections (5, 6), however, the tissue specificity is not absolute (7). HSV-2 can be isolated occasionally from the oropharynx and 5-10% of primary genital infections may be caused by HSV-1. Infants infected with HSV appear normal at birth, but almost invariably develop symptoms during the newborn period (5, 8, 9). Neonatal HSV infection may remain localized or become disseminated. Localized infection may involve one or a combination of sites. These are skin, eyes, mouth or the central nervous system. Disseminated infection is manifested by pneumonitis, hepatitis, disseminated intravascular coagulopathy and encephalitis. Of the infants with neonatal HSV, about one half of those surviving will develop severe neurological or ocular sequelae. A number of serological procedures have been developed to detect antibodies to HSV. These include complement fixation, indirect immunofluorescent antibody, plaque neutralization, and ELISA (6, 8, 10). Antibody of the IgG class is produced during the first 2-3 weeks of infection with HSV and exists only transiently in most patients. Serologic procedures, which measure the presence of IgG antibodies, help discriminate between primary and recurrent infections, since IgG antibodies is rarely found in recurrent infections. High affinity IgG antibodies to HSV, if present in a sample, may interfere with the detection of IgG specific antibody (9). High affinity IgG antibody may preferentially bind to HSV-1 antigen leading to false negative IgG results. Also, rheumatoid factor, if present, along with antigen specific IgG, may bind to IgG causing false positive IgG results. Both problems can be eliminated by deactivating IgG in the sample before testing for IgG.

The Cytomegalovirus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of Cytomegalovirus (CMV) in human serum/plasma samples.

Cytomegalovirus is a herpes virus and a leading biological factor causing congenital abnormalities and complications among those who receive massive blood transfusions and immunosuppressive therapy. About half of the number of pregnant women who contract a primary infection, spread the disease to their fetus. When acquired in-utero, the infection may cause mental retardation, blindness, and/or deafness. Serological tests for detecting the presence of antibody to CMV can provide valuable information regarding the history of previous infection, diagnosis or active or recent infection, as well as in screening blood for transfusions in newborns and immuno-compromised recipients.

The Cytomegalovirus Rapid Test Device (Serum/Plasma) has been designed to detect CMV through visual interpretation of color development in the internal strip. The membrane was immobilized with antigens of CMV on the test region. During the test, the specimen is allowed to react with colored recombinant mouse anti-human IgM latex conjugates, which were precoated on the sample pad of the test. The mixture then moves on the membrane by a capillary action, and interact with reagents on the membrane. If there were enough CMV antibodies in specimens, a colored band will from at the test region of the membrane. Presence of this colored band indicates a positive result, while its absence indicates a negative result. Appearance of a colored band at the control region serves as a procedural control. This indicates that proper volume of specimen has been added and membrane wicking has occurred.

Intended Use

The One Step Rv Igg/igm Test Is A Rapid Chromatographic Immunoassay For The Qualitative Detection Of Antibodies (igg And Igm) To Rubella (virus) In Whole Blood /serum / Plasma To Aid In The Diagnosis Of Rv Infection. The Test Is Based On Immunochromatography And Can Give A Result Within 15 Minutes.

Principle

The One Step RV IgG/IgM Test is a qualitative membrane strip based immunoassay for the detection of RV antibodies (IgG and IgM) in Whole Blood /Serum / Plasma. The test device consists of: 1) a burgundy colored conjugate pad containing RV recombinant envelope antigens conjugated with Colloid gold (RV conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-RV, T2 band is coated with antibody for the detection of IgG anti-RV, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-RV, if present in the specimen, will bind to the RV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a RV IgG positive test result and suggesting a recent or repeat infection. IgM anti-RV if present in the specimen will bind to the RV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a RV IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device.

Storage and Stability

Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch.

The test must remain in the sealed pouch until use.

Product Name:
Surplex(R)-COVID-19 IgM/IgG Rapid test

Product Description:
Surplex(R)-COVID-19 IgM/IgG Rapid test is a serology test intended for the qualitative detection of IgM and IgG antibodies of the novel coronavirus (the SARS-COV-2 virus) in human serum, plasma or whole blood. It is CE marked and approved in Brazil (ANVISA approved).
We are motivated to aggressively price our product and ready to send 20 tests (one box) to qualified buyers for evaluation, free of charge.

Price of product:
FOB USD $1.50 - $2.50 per test, volume dependent.

Product origin :
China.

Key Specifications/Special Features :
- Competitively priced and ready to ship in volume.
- Currently shipping in volume to Brazil.
- Highly accurate and specific - performance independently confirmed.
- Results ready in 15 minutes.
- Harmonization System (HS) Code: 382200.
- We provide a full support during regulatory application.

Minimum Order Size and Packaging details:
MOQ: Flexible.
Box of 20 or 50 test kits.
Storage: 2-30C.
Shelf Life: 10 months.

The CLIA Waived COVID-19 IgG/IgM Rapid Test Device is an in vitro immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood, serum, or plasma. The test is for professional use only.

Indication:

Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, or plasma (sodium EDTA). Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. Emergency use of this test is limited to authorized laboratories.

About Test Device

EUA Authorized
CE Mark
Gives Positive or Negative Result for COVID-19 virus
Read Results in 15 Minutes
24 Month Expiration from Date of Manufacture
Contents

20 Test Devices
20 Disposable Pipettes
20 Alcohol Prep Pads
Sterile Safety Lancets
Buffer
Package Insert

Product Name
Corona-virus (SARS-CoV-2) (IgM / IgG) Diagnostic Kit
Packing Specifications
1 test/bag, 1 test/box, 20 tests/box, 50 tests/box.
Intended Use
This kit uses immunocolloidal gold chromatography to detect novel coronavirus IgM/IgG antibodies in human serum, plasma or whole blood in vitro.
The 2019 novel coronavirus, abbreviated as 2019-nCov, is a new strain of coronavirus discovered in the human body and outbreaked in Wuhan in the end of 2019. The symptoms of the virus are fever, fatigue, dry cough, and progressive dyspnea. In severe cases, the symptoms are acute respiratory distress syndrome, septic shock, metabolic acidosis and coagulation dysfunction that canot be reversed. The virus has been confirmed the capacity of human-to-human transmission; the shortest incubation period of the virus is only 1 day, while the longest is 14 days. The patients in incubation period is contagious and there is no specific treatment for the disease. Once infected with a new virus, the body's immune system will start to defend and produce specific antibodies. Generally, IgM antibody will appear in 1-2 weeks and IgG antibody will appear in 4 weeks.

SOFTEC COVID-19 IGG/IGM Antibody Test Kit (Single Pack)
The COVID-19 IgG/IgM Rapid Test Cassette is a lateral flow chromatograpic immunoassay for the qualitative defection of antibodies (IgG and IgM) to Novel coronavirus in human Whole Blood/Serum/Plasma. It provides an aid in the diagnosis of intection with Novel coronavirus.

A serology test or Antibody Rapid Test which doesn't test for the virus itself. Instead, it look for body's immune response to the virus. This test is getting popular is not only because its convenience but also because it can identify whether youâ??ve ever been exposed to SARS-CoV-2 - which would deepen our understanding of who is getting sick, particularly people who showed few or no symptoms. It could also allow people whose bodies seem to have some degree of immunity to the illness to return to work more quickly.

Please email us and get detailed factsheet, certification etc.

SARS-CoV-19 IgG/IgM test kit (15min showing result)
Manufacturer: Guangzhou Wanfo Biotech Co., Ltd. a China listing company
Certificates: CE certificate, China NMPA approval (export allowed), no FDA approval
The price is $5.5/test (FOB)
Max delivered quantity: 100,000/weekly

ImmunoQuick Covid-19 IgM/IgG Test :

Covid-19 or commonly known as Coronavirus is a viral infection involving a patients upper respiratory tract. It is highly contagious and causes a severe lung infection which can be severely debilitating and sometimes fatal. Our test detects two types of antibodies to Covid-19 which appear from 2 to 21 days after infection. It is an invaluable test to diagnose people who have been sick for a few days or those who have recovered.



Salient Features of the Product

It is rapid immunoassay for qualitative detection of Covid-19 IgM and IgG antibodiesin

Human Serum or Plasma or Whole Blood.

Results available in 15 minutes.

Sensitivity :: >96%

Specificity :: >99%

No cross reactivity observed.

Can be stored at 4 to 30C

Stable for 24 months.

Pack size :: 25 tests.

Intended use

The test kit utilize purified chlamydia trachomatis antibody antigen, based on gifa principle and use indirect method to detect urea plasma urealyticum antibody in human serum.


Test procedure

1. Remove the test kit and put it at room temperature (for about 20-30mins) before testing.

2. Add 1 drop of wash buffer into the hole and allow the liquid soak the membrane completely.

3. Add 150the serum specimen into the hole and allow it to sufficient absorption.

4. Add 3 drops of colloidal conjugate into the hole and allow it to sufficient absorption.

5. Add 3 drops of wash buffer into the hole and allow it to sufficient absorption. Read the results within 3 minutes.

Storage

The kit can be stored at room temperature. The test kit is stable through the expiration date (18 months) marked on the foil pouch. Do not freeze. Do not store the test kit in direct sunlight.

Product Details:

Number of Reactions(Preps)/Kit : 10
Brand : CTK BioTech
Result Time (Rapid Kits) :15 min
Sample Type :Blood
Test Type Rapid Test
CAT No : R0092C
Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patient's visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC

Individually sealed foil pouches containing:
One cassette device
One desiccant
5 Aul capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use)

Product Details:
Number of Reactions(Preps)/Kit : 30T
Brand : CTK Biotech
Result Time (Rapid Kits) : 15 mins
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0160C
The OnSite Typhoid IgG/IgM Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.

Product Description:

Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
Differentiates Between Igg And Igm To Determine Stage Of Infection
One Step Procedure Minimizes Operator Error Due To Sample Preparation
High Level Of Reproducibility
Test Kits Can Be Used And Stored In A Wide Range Of Temperatures

Product Specification:-

Brand Name : CTK Biotech
Pkg Qty : 1
Number Of Items : 30
Specifications : Test Result Within 15 Minutes Allows Medical Professionals To Take Immediate Action
Contains1 : Individually Sealed Foil Pouches Containing:One Dip Strip Device,One Desiccant,Plastic Droppers,Sample Diluent (ref Sb-R0160, 5 Ml/Bottle)

CAT No : R0160C. The OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.

Product Description
Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
Differentiates Between Igg And Igm To Determine Stage Of Infection
One Step Procedure Minimizes Operator Error Due To Sample Preparation
High Level Of Reproducibility
Test Kits Can Be Used And Stored In A Wide Range Of Temperatures

CLIA Waived

Use of this test with all authorized specimen types is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity tests.

This test is also authorized for use with fingerstick whole blood specimens only at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.

The COVID-19 IgG/IgM Rapid Test Device is an in vitro immunoassay for the direct and qualitative detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG in human whole blood, serum, or plasma. The test is for professional use only.

Indication:

Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, or plasma (sodium EDTA). Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection.

About Test Device

EUA Authorized
Gives Positive or Negative Result for COVID-19 virus
Read Results in 15 Minutes
24 Month Expiration from Date of Manufacture
Contents

20 Test Devices
20 Disposable Pipettes
20 Alcohol Prep Pads
Sterile Safety Lancets
Buffer
Package Insert

SGTi-flex Rapid Antibody Test

COVID-19 IgM/IgG Antibody Detection Kit (Colloidal Gold Immunochromatography) is suitable for the qualitative detection of COVID-19 by detecting SARS-CoV-2 IgM/IgG antibodies in human serum, plasma, or whole blood. Common signs of infection with SARS-CoV-2 include respiratory symptoms, fever, cough, shortness of breath, and dyspnea. In more severe cases, infection can cause pneumonia, severe acute respiratory syndrome, kidney failure, and even death. SARS-CoV-2 can be excreted through respiratory secretions or transmitted through oral fluids, sneezing, physical contact, and through air droplets

Cat No: RK056-20. STANDARD Q COVID-19 IgM/IgG Combois a rapid Immunochromatographic assay for the qualitative dtection of specific antibodies to SARS-CoV-2 present in human Serum,Plasma or Whole Blood specimen.

Rapid testing for detection of IgM & IgG antibodies against SARS CoV-2
10 µl of specimen: Serum, Plasma & Whole Blood
Long term storage of 24 months at 2 - 30 C
Complementary to RT-PCR Test
Can be performed without extra equipment

High accuracy High quality, with CE certificate.
10 tests per box

The outbreak of the novel coronavirus (COVID-19) rapidly transmit all over China and lots of countries. Although molecular test (RT-PCR) has become the standard method for diagnosis of this disease, the method has many limitations. In addition, the high false negative rates were reported.

There is an urgent need for an accurate and rapid testing method that quickly identify large number of infected patients and asymptomatic carriers to prevent virus transmission and assure timely treatment of patients.

GenBody COVID-19 IgM/IgG device is a chromatographic immunoassay kit for the rapid and differential detection of immunoglobulin M (lgM) and immunoglobulin G (IgG) against COVID-19 using serum, plasma and whole blood.

Uncut Sheet Strep A IgG/IgM Rapid Test

Format:Cassette/Strip Uncut Sheet

A rapid test for the qualitative detection of Strep A antigen in throat swab specimens.For professional in vitro diagnostic use only.

Intended Use

The Strep A Rapid Test Strip (Throat Swab) is a rapid chromatographic immunoassay for the qualitative detection of Strep A antigen from throat swab specimens to aid in the diagnosis of Group A Streptococcal infection.

Summary

Streptococcus pyogenes is non-motile gram-positive cocci, which contains the Lancefield group A antigen that can cause serious infections such as pharyngitis, respiratory infection, impetigo, endocarditis, meningitis, puerperal sepsis, and arthritis.1 Left untreated, these infections can lead to serious complications, including rheumatic fever and peritonsillar abscess.2 Traditional identification procedures for Group A Streptococci infection involve the isolation and identification of viable organisms using techniques that require 24 to 48 hours or longer.3,4

The Strep A Rapid Test Strip (Throat Swab) is a rapid test to qualitatively detect the presence of Strep A antigen in throat swab specimens, providing results within 5 minutes. The test utilizes antibodies specific for whole cell Lancefield Group A Streptococcus to selectively detect Strep A antigen in a throat swab specimen.

PRINCIPLE

The Strep A Rapid Test Strip (Throat Swab) is a qualitative, lateral flow immunoassay for the detection of Strep A carbohydrate antigen in a throat swab. In this test, antibody specific to Strep A carbohydrate antigen is coated on the test line region of the test. After the test strip is immersed into a specimen, the extracted throat swab specimen reacts with an antibody to Strep A that is coated onto particles. This mixture migrates up the membrane to react with the antibody to Strep A on the membrane and generate a colored line in the test line region. 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 at the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.

Uncut sheet leishmania igg/igm rapid test

Specimen:whole blood/ serum/ plasma

Intended use

The leishmania igg/igm rapid test is a lateral flow immunoassay for the qualitative detection of antibodies including igg and igm to the subspecies of the leishmania donovani (l. Donovani), the visceral leishmaniasis causative protozoans in human serum or plasma. This test is intended to be used as a screening test and as an aid in the diagnosis of the disease of visceral leishmaniasis. Any reactive specimen with the leishmania igg/igm rapid test must be confirmed with alternative testing method(s).

Summary and explanation of the test

Visceral leishmaniasis, or kala-azar, is a disseminated infection caused by several subspecies of the l. Donovani. The disease is estimated by the world health organization (who) to affect approximately 12 million people in 88 countries1. It is transmitted to humans by bites of the phlebotomus sandflies, which acquire infection from feeding on infected animals. Though it is a disease for poor countries, in southern europe, it has become the leading opportunistic infection in aids patients2-3.

Identification of l. Donovani organism from the blood, bone marrow, liver, lymph nodes or the spleen provides a definite means of diagnosis. However, these test methods are limited by the sampling method and the special instrument requirement. Serological detection of anti-l. Donovani ab is found to be an excellent marker for the infection of visceral leishmaniasis. Tests used in clinic include: elisa, fluorescent antibody and direct agglutination tests4-5. Recently, utilization of l. Donovani specific protein in the test has improved the sensitivity and specificity dramatically6-7.

The leishmania igg/igm rapid test is a recombinant protein based serological test, which detects antibodies including igg, igm and iga to the l. Donovani. This test provides a reliable result within 10 minutes without any instrumentation requirements.

General Information
One-Step Leishmania IgG/IgM Rapid Test is detection antibodies IgG and IgM to the subspecies of the Leishmania donovani (L. donovani), the Visceral leishmaniasis causative protozoans in human blood.
Sensitivity: 91.2 % , Specificity: 99.5%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 min

General Information
One-Step Chikungunya IgG/IgM Rapid Test is detection of IgG and IgM anti-chikungunya virus CHIK in human blood.
Sensitivity: 90.3% , Specificity: 100%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 min

INTENDED USE
For qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in serum, plasma (EDTA, sodium citrate and lithium heparin) or fingerstick whole blood, venous whole blood specimens from patients suspected of COVID-19 infection.

FEATURES
Coated with carefully selected specific Nucleocapsid and Spike protein antigen.
Detection for IgM and IgG antibodies simultaneously.
Simple operation, easy result interpreted.
Rapid test within 15 minutes.

RESULTS INTERPRETATION
Positive:
1. The presence of 3 red lines (T1, T2 and C) within the reaction window, no matter which band appears first, indicates presence of both SARS-CoV-2 IgM and IgG antibodies.
2. The presence of 2 red lines (T1 and C) within the reaction window, no matter which band appears first, indicates presence of SARS-CoV-2 IgM antibody.
3. The presence of 2 red lines (T2 and C) within the reaction window, no matter which band appears first, indicates presence of SARS-CoV-2 IgG antibody.

Negative:
1. The presence of line (control line) only within the reaction window indicates that no SARS-CoV-2 antibodies are detected. The results is negative.

Invalid:
1. If the control(C) line is not displayed in 10-15 min, regardless of whether T1 and/or T2 line is present, the test result is invalid. It is recommended that the specimen should be re-tested.
2. The test result is invalid after 15 min.

CLINICAL PERFORMANCE
- Positive Percent Agreement (PPA) = 91.07% (153/168) (95% CI: 85.70%-94.92%).
- Negative Percent Agreement (NPA) = 95.37% (103/108) (95% CI: 89.53%-98.48%).
- Overall Rates of Agreement (ORA) = 92.75% [(153+103)/ (168+108)] (95% CI: 89.03%-95.52%).

[Product Name]: SARS-CoV-2 IgM/IgG Duo Test
[Product Code]: Cat# FP-319
[Sample Type]: Whole blood /Plasma/Serum
[Sample Volume]: 20L /10L/10L
[Detection Method]: Colloidal Gold
[Reaction Time]: 10-15min
[Packing Size]: 1T x 20 cassettes per box + Sample diluent 1 vial x 5mL.
[Storage Condition]: 2oC ~ 30oC
[Shelf Life]: 12 months
[CE Mark Registration No.]: RPS/499/2021.

This product is the rapid testing of COVID-19, the result come out within 10 minutes.

Product Details:

Number of Reactions(Preps)/Kit 30T
Brand CTK Biotech
Result Time (Rapid Kits) 20mins
Test Type Rapid Test
CAT No : R0234C
The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.

Product Details:
Number of Reactions(Preps)/Kit 30
Brand : CTK BioTech
Result Time (Rapid Kits) :20-25 Min
Sample Material :Serum / Plasma / Whole Blood
Cat. No : R0061c
The OnSite Dengue IgG/IgM 3.0 Combo Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM antiâ??dengue virus (DEN1, 2, 3 and 4) in human serum, plasma or whole blood.

Product Features:
Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 AUL Capillary tubes
Sample diluent (REF SB-R0061, 5 mL/bottle)
One package insert (instruction for use)

Product Details:

Number of Reactions(Preps)/Kit : 30T
Brand : CTK BioTech
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0101C
Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market
Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA
Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3,000 U/L; Creatinine: 442 �¼mol/L; Bilirubin: 20 mg/dL; EDTA: 3.4 �¼mol/L; Hemoglobin: 2g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L
Shelf life: 24 month

Individually sealed foil pouches containing:
One cassette device
One desiccant
5L capillary tubes
Sample diluent (REF SB-R0101, 5 mL/bottle)
One package insert (instruction for use)

The iFinDx COVID-19 IgM/IgG is a rapid test kit for differential detection of specific IgM and IgG against COVID-19 in human serum, plasma and whole blood.

Warranty:2 years, 2 Years After-sale Service:Online Technical Support Material:Plastic Shelf Life:2 years Quality Certification:CE Instrument classification:Class II Safety standard:MFDS Product name:antibody test Sensitivity: >85% Specificity: >90% Total coincidence rate: >90% Work environmental temperature: 40 Inspection method:antibody detection Sample dosage:10ul Inspection time: 15min Type of sample:capillary vessel or vein

Uncut sheet toxoplasma gondii igg/igm tri-lines rapid test

Specimen :whold blood/serum/plasma

Intended use

The one step toxo igg/igm test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (igg and igm) to toxoplasma gondii in whole blood /serum / plasma to aid in the diagnosis of toxo infection. Toxoplasma gondii is an obligate intracellular protozoan parasite with a worldwide distribution. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism. A variety of serologic tests for antibodies to toxoplasma gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are the sabin-feldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluorescence, and elisa. Recently, lateral flow chromatographic immunoassay, such as the toxo igm/igg rapid test (whole blood/serum/plasma) was introduced into the clinic for the serodiagnosis of toxoplasma gondii infection. One step toxo igg/igm test is a simple, visual qualitative test that detects toxo antibodies in human whole blood/serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes.

Storage and stability

Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch.

The test must remain in the sealed pouch until use.

General Information
One-Step Dengue Rapid Test is to detect IgG&IgM antibodies in serum, plasma or whole blood.
For Dengue IgG/IgM Ab test:
Sensitivity : 99.9% , Specificity : 99.5%
Specimen : Serum , Plasma and Whole Blood
Reading Time : 10 min

Product Details:

Number of Reactions(Preps)/Kit 30T
Brand CTK BioTech
ICMR Approved Yes
Result Time (Rapid Kits) 20min
CAT No : AR5001C
Details :
Utilizes Recombinant Orientia tsutsugamushi antigens.
Qualitative detection and differentiation of antibodies(IgG and IgM) against Orientia tsutsugamushi (Scrub typhus)
Compatible with Whole blood, Serum and Plasma.
Sensitivity: For IgG 95.4% and IgM 96.1%, Specificity: For IgG 96.8% and IgM 97.6%.
Results in 20 minutes.

Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Detection buffer (tris-based buffered solution with preservatives)
Instructions for Use

Product Details:
Number of Reactions(Preps)/Kit : 10T
Brand : CTK BioTech
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : AR0151C
Use of conserved antigens allows pan-filaria tests to be applicable
Simple procedure provides alternative to diagnosis by blood smear
Use serum, plasma or whole blood
No restrictions on time of day for sample collection
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Plastic droppers
Sample diluent (1 bottle, 5 mL)
One package insert (instruction for use)

Product Details:

Number of Reactions(Preps)/Kit : 10T
Brand : CTK BioTech
Result Time (Rapid Kits) : 10 min
Sample Type : Blood
Test Type : Rapid test
CAT No : R0063C
Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection

Individually sealed foil pouches containing:
One cassette device
One desiccant
5 auL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)

Intended Use

The One Step HAV IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Hepatitis A Virus (HAV) in Whole Blood /Serum / Plasma to aid in the diagnosis of Hepatitis A Virus.

Summary

Hepatitis A is an acute, usually self-limiting disease of the liver caused by hepatitis A virus (HAV). HAV is transmitted from person to person, primarily by the faecal-oral route. The incidence of hepatitis A is closely related to socioeconomic development, and seroepidemiological studies show that prevalence of anti-HAV antibodies in the general population varies from 15% to close to 100% in different parts of the world. One step HAV IgG/IgM Test is a simple, visual qualitative test that detects Hepatitis A Virus antibodies in human Whole Blood /Serum / Plasma. The test is based on immunochromatography and can give a result within 15 minutes.

Principle

The One Step HAV IgG/IgM Test is a qualitative membrane strip based immunoassay for the detection of Hepatitis A Virus antibodies (IgG and IgM) in Whole Blood /Serum / Plasma. The test device consists of: 1) a burgundy colored conjugate pad containing HAV recombinant envelope antigens conjugated with Colloid gold (HAV conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-HAV, T2 band is coated with antibody for the detection of IgG anti-HAV, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-HAV, if present in the specimen, will bind to the HAV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a HAV IgG positive test result and suggesting a recent or repeat infection. IgM anti-HAV if present in the specimen will bind to the HAV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a HAV IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device.

Storage and Stability

Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch.
The test must remain in the sealed pouch until use.

Product Details:

Number of Reactions(Preps)/Kit 25 Test
Brand SD Biosensor
Result Time (Rapid Kits) 15 Min
Cat. No 09LEP10D
STANDARD Q Leptospira IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Leptospira interrogans in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage
Differential detection of IgG and IgM antibodies
Easy to use, Easy to read and interpret
Room temperature storage of 2-40 / 36-104
Able to read positive/negative infections fast and accurately with a little amount of sample (10 µl).

Product Details:
Number of Reactions(Preps)/Kit : 20T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK024-20
STANDARD Q Chikungunya IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Chikungunya virus in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Differential detection of IgG and IgM antibodies
Easy to use, Easy to read and interpret
Room temperature storage
Able to read positive/negative infections fast and accurately with a little amount of sample (10 aul)

Product Details:
Number of Reactions(Preps)/Kit : 20T
Brand ; SD Biosensor
ICMR Approved ; Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK029-20
STANDARD Q TSUTSUGAMUSHI IgM/IgG is a rapid,sensitive,qualitative Immunochromatographic assay for the detection of IgM/IgG antibodies against Orientia Tsutsugamushi in human serum,Plasma or whole blood specimen.it is an initial screening test and this test kit is for in vitro use only by professionals.

Differential detection of IgM & IgG Antibodies
Easy to use,Easy to interpret
Long term storage
Faster results with lesser specimen volume (10aul)

Product Details:
Number of Reactions(Preps)/Kit :20T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15min
CAT No : RK012-20
One step, rapid, immunochromatographic test for the detection of Dengue IgMlIgG antibodies to four senatypes of dengue virus (DEN-I, DEN-2. DEN-3 and DEN-4) in human serum, plasma or whole blood.
Kit Contents:
Standard Q Dengue IgM IgG cassette x 20
Specimen transfer device 10ml x 20
Butter bottle 4ml x 01
Instructions for use x 1
STANDARD Q Dengue IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Dengue virus in serum, plasma and whole blood using immunochromatography. By detecting IgM and IgG specific to Dengue virus, the primary and secondary Dengue virus infections can be discriminated, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.

Advantage:
Differential detection of IgG and IgM antibodies
Easy to use, Easy to read and interpret
Room temperature storage
Able to read positive/negative infections fast and accurately with a little amount of sample (10 �µl)

CAT No : R0063C. Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection Individually sealed foil pouches containing:
One cassette device
One desiccant
5 uL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)

Corona viruses are enveloped RNA viruses that are distributed broadly among humans, birds and other mammals, that cause respiratory, enteric, hepatic, and neurologic disease.

SPECIFICATIONS:

Whole blood/serum/plasma may be used for testing.

Results available in only 15 minutes.

Easy to use.

Result can be read visually.

No need for an analyser.

Cost effective method for assisting in screening COVID-19 disease.

Clarification of a possibly already occurred immune reaction of the body against SARS-CoV-2 by determination of the specific IgM and/or IgG immunoglobulins (Antigens: S1, S2 and N Proteins).

Price-Details:
25% discount for government, clinics and medical facilities. Companies will only receive the discount if they can prove that they use the product for their own purposes and not for commercial purposes. Ask for special deal for 1,000,000 units and more.

Performance:
The rapid test has a very high accuracy because - unlike most rapid blood tests and laboratory tests - it uses 3 proteins (S1, S2 and N) to detect the antibodies (so-called trinity method). The significance of the rapid test increases during the course of the infection with the formation of antibodies in the blood (between day 4-11 in about
70% of patients).

The overall sensitivity of the test (IgM/IgG) is 98.6% (> 1,100 clinical trials).
The specificity of the test (reaction only to Covid19) is 99.5% (> 1,500 clinical trials).
Please compare this with other tests!

Advantages
Quick result: The rapid test shows a significant result within 20 minutes.
Test procedure: We provide a simple and fast test procedure with two drops of blood from the fingertip, from venous blood or from unfrozen serum.
Certified Quality: The test is â??Made in Germany with CE conformity declaration and fulfils the FDA & WHO-requirements.

What is included per unit:
1x Cassette (Polystyrene)
1x Support Pad (PVC 3.0 x 60 mm)
1x Cellulose Nitrate Membrane (Cellulose nitrate membrane coated with mouse, anti-human IgM and IgG antibodies)
1x Specimen Pad (Glass fiber / GF)
1x Liquid Absorption Pad (Cellulose acetate membrane)
1x Chemical Coupling Pad (Sealed glass fiber, coated with SARS-CoV-2 antigens and mouse IgG controls)
2g Desiccant (Molecular sieve desiccant)
1x, Aluminum Foil Package (12 x6.5 cm, three-layers of aluminum foil paper)
1x Tag (80 x 50 mm, single-sided plastic tag)
1x Sealable Bag (A sealable bag for disposal of the used cassette)
1x Lancet (Lancets for fingerstick whole blood only)
1x Plastic pipette (A transfer plastic pipette with the line mark of 50 )
1x Squeezable plastic liquid dropper ampoule (Plastic ampoule containing dilution buffer 1)
1x Instructions for Use