We are the authorized first vendor of ADTech!
KFDA CE approved,
FDA Pending
Price : Negotiable
Pre-Clinical Test Report
Accuracy
- In total samples 93.3% (14/15) - In positive samples 91.7% (11/12)
1. Pre-Clinical Test summary
1) Pre-clinical test is fulfilled by Domestic large clinical laboratory with ADTech COVID-19 IgM/IgG RAPID KIT
2) Tests are made by total 15 samples with 12 positive and 3 negative samples
3) Clinical Laboratory tested the sample with Immunofluorescence Analysis
2. Pre-clinical test result
1) Samples were tested by ADTech COVID-19 IgM/IgG RAPID KIT
2) Test result by ADTechs RAPID KIT
- 4 negatives and 11 positives results in 15 samples
3) Comparison between Immunofluorescence analysis and ADTechs RAPID KIT
- 14 test results are same(including negative and positive results) - 1 samples test result are different(Positive Negative by ADTech
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.
Livzon Rapid Test for SARS-CoV-2 Antigen (Lateral Flow)
Livzon Rapid Test for SARS-CoV-2 Antigen (Lateral Flow) is used for in vitro qualitative
detection of SARS-CoV-2 nucleocapsid antigen in nasopharyngeal swabs, oropharyngeal swabs
and nasal swabs from individuals who are suspected of SARS-CoV-2 by their healthcare
provider within the first seven days of symptom onset.
Angiten-COVID-19 Virus Test Kit (Colloidal Gold)
Quantity of box: 25 persons/box
Brand: Easysweet
NMPA (National Medical Products Administration): Approved
CE: with CE mark
BfArM: listed
Test Method: Antigen Test
Result Time: 10-15 mins
Sample Type: Nasal Swab
Sensitivity: 96.70%
Specificity: 100%
Accuracy: 98.94%
Shelf Life: 24 months
Storage Temperature: 2-30 Degree Celsius
Country of Origin: Made in China
Additional Information:
Production Capacity: 1 million
Delivery Time: 10-15 days
Packaging Details: 25 tests in a pack, 40packs/ carton
Angiten-COVID-19 Virus Test Kit is an in vitro diagnostic rapid test for the qualitative detection of SARS-CoV-2 antigen (Ag) in human nasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. It can be used by professional only.
Price and Minumum Quantity
Price FOB in USD: NegotiableMinimum Order Qty: 10000
Production Capacity: 1000000Packaging: 25 Persons/box
Sample: Available. Sample Cost Born By Buyer
Product Model And Origin
Brand: Easysweet
HS Code: 3822009020
Standards: Ce
Competitive Advantages
Best price with shortest delivery time
Best price with shortest delivery time
Best price with shortest delivery time
Best price with shortest delivery time
Other Details
Angiten-covid-19 virus test kit (colloidal gold)
Angiten-covid-19 virus test kit (colloidal gold)
Angiten-covid-19 virus test kit (colloidal gold)
Angiten-covid-19 virus test kit (colloidal gold)
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Covd-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) is a solid phase immunochromatographic assay for the rapid, qualitative and dierential detection of IgG and IgM antibodies to 2019 Novel Corona Virus in human whole blood, serum or plasma.
Specification.jpg
Product: Rapid Diagnostic Test Kit
Item: Corona Virus Test Kit
Specimen: Whole Blood/Serum/Plasma
Format: Strip/Cassette
Port of Loading: Shanghai
OEM and ODM: OEM/ODM Welcome
Shipping: By UPS, FEDEX, DHL, TNT, by air or by sea
Note: Store this product in a cool and dry place, avoid direct sunlight, stay away from places that children can contact, and avoid eye contact. If you have allergies to this product, please stop using and consult a doctor.
COVID-19 Corona Virus Rapid Test Kit11.pngCOVID-19 Corona Virus Rapid Test Kit12.png
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
Access Bio Care Start Covid-19 Rapid Antigen Test Kit
Product Details:
Number of Reactions(Preps) per Kit : 1
Brand : Access Bio
Test Method : Antigen Test
Result Time (Rapid Kits) : 10 min
Sample Type ; Nasal Swab
Packaging Size : 20 Test Kits/Box
Packaging Type : Box
The CareStart COVID-19 Antigen test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals who are either suspected of COVID-19 by their healthcare provider within first five days of symptom onset, or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between
Indiaâ??s first COVID-19 test kit for self-use. Get your test results within 15 min from the comfort of your home & Office.
So, there might be a time when you think you have contracted COVID-19 but cannot book a slot for an RT-PCR test. You might be asked to wait a couple of days. In such a circumstance, you can avail of a home/office corona testingÃ? kitÃ? such as Mylab CoviSelf COVID-19 RapidÃ? Antigen Test for COVID.Ã?Â
It is Indiaâ??s first COVID-19 home test kit to have earned the approval of the ICMR. Anyone above the age of 18 can use it at home. However, adult supervision is suggested if the test kit is used by people below 18.
Intelligently Designed
Filled with a solution that inactivates the virus and is designed in a manner to control & contain biohazard.
BOSON - Rapid SARS-CoV-2 Antigen Test - Pack of 5 Available at 0.75 EUR Plus VAT and Transport per test IFU - Swedish, Finissh, Norwagian, English, Danish
Product Descirption :
"A home test for the rapid qualitative detection of SARS-CoV-2 virus antigen in
anterior nasal swabs from individuals with or without symptoms or other
epidemiological reasons to suspect COVID-19
Performance Characteristics:
Sample type: nasal swab
Time to result: 15-20 min
Sensitivity - 97.70%
Specificity - 99.84%
Accuracy - 98.97%
UK MHRA - DHSC Approved for Self Test
Approved in Germany, France, Italy, Belgium, Netherlands, Greece, Spain, Portugal.
Layperson study statistics:
99.84% of non-professionals carried out the test without requiring assistance
99.82% of different types of results were interpreted correctly
*Ex works price is around $5.5 per kit all in inclusive 4cents commissions for all the brokers.
*Made in Korea, *Celltrion is a very well-known large corporation in Korea, and is one of the few companies that has been approved by the US FDA. *Detailed consultation is possible when submitting LOI.
DiaTrustâ?¢ COVID-19 Ag Rapid Test- 156 pallets available. 748,800 tests are readily available for pickup.
Distrust covid-19-ag rapid antigen test 25ct box $9.35 ea test.
The Pathocatch Coviself Covid - 19 Rapid Antigen test (RAT) is an in vitro diagnostic test for the qualitative detection of covid - 19 antigen in nasal swab specimens directly from individuals with or without symptoms or other epidemiological reasons to suspect COVID-19.
Hello,
I hope you are doing well.
We have the following test kits.
If you are interested please send an LOI:
Outfront Marketing Medical LLC
Doug@Outfrontmarketing.com
Please include a location for delivery.
We will then send you a formal Invoice and Instructions.
These kits are selling fast.
We have an allotment of 30M available 1/15/22.
So place an order asap.
MOQ 50K
Covid-19 Rapid Test Kits Results in 15 Min - MOQ 100,000- $9.15 USD Each Test -FOB-Abbott Antigen BinaxNOW Covid-19 Self Test (Nasal) (No Blood-No Saliva)
BOSON RAPID SARS CoV-2 Antigen Test Card (Self Test) Manufactured by Xiamen Boson Biotech Co., Ltd.
DHSC - UK Approved - 3rd Phase Approved.
NASAL TEST
CE & ISO Approved
Full Home Test - Self Test Approval for UK and Europe
Test Result in 15 Minutes.
Sensitivity 97.70%
Specificity 99.84%
Accuracy 98.97%
Layperson study statistics
99.84% of non-professionals carried out the test without requiring assistance
99.82% of different types of results were interpreted correctly
Each Test have Unique Identifier Number - Easy to track
Approved By - UK, Germany, France, Spain, Netherlands, Greece, Belgium, Italy, Portugal.
1 Test / Kit
Catalog No.: 1N40C5-2
Kit Components:
1 Rapid SARS-CoV-2
Antigen Test Card (sealed
foil pouch)
1 sterilized swab
1 extraction tube
1 sample extraction buffer
IFU
Tube holder on back of box
Box / Carton Specifications :
1 Test / Kit
Box size - 190*60*15 mm
Carton size - 42*42*33 cm
Carton gross weight - 9.9 kg
250 tests (boxes) / carton
For in vitro qualitative detect of Covid-19 antigen in nasal(NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days of the onset of the symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, and not for at home testing.
1.Easy to collect samples simple operation without professional equipment.
2.The test results are available in 15 minutes, and the test results are clearly visible. 3.Convenient transportation and low price, higher accuracy.
4.Suitable for large-scale rapid screening.
Shelf life: 24 Months
Test Result time: 10 Mins
Packing: 25 Pieces per Box
Our Rapid Typhoid Testing Kit is a cutting-edge solution for swift and accurate diagnosis of typhoid fever. This advanced kit is designed for quick detection of the Salmonella Typhi bacteria, streamlining the diagnostic process for healthcare professionals.
With a user-friendly approach, it requires a small blood sample and delivers results within minutes, enabling rapid treatment decisions. The kit exhibits exceptional sensitivity and specificity, ensuring reliable diagnoses even in low-infection scenarios. Its compact, portable design makes it ideal for remote and resource-limited areas. Trust our Rapid Typhoid Testing Kit for fast, dependable, and life-saving typhoid fever diagnosis, enhancing patient care and containment of this infectious disease.
The self testing product is transformed from the professional testing product
CLUNGENE COVID 19 Antigen Rapid Test manufactured by Clongene
The BfArM has granted the first special approvals according to 11 paragraph 1
of the German Medical Devices Act ( of antigen tests for self administration by laypersons (self tests) for the detection of SARS CoV 2 Our self testing product can be sold and
used in Germany Overview of CLUNGENE COVID 1
Product Name -
Realy Tech" Rapid Coronavirus Antigen Test (sars-cov-2) -
Product Description -
Specifications
Test duration: 15 minutes
Sample type: nasopharyngeal swab.
Storage: at room temperature or refrigerated (2-30 C)
Expiration: 24 months ex works
Key Specifications/Special Features -
25 test boxes: Each test box is packed in an aluminum foil bag with desiccant.
25 extraction reagents: vial with 0.3 ml extraction reagent
25 sterilized swabs: disposable swabs for sample collection
25 extraction tubes
25 dropper tips
1 work station
1 leafle
Product Name -
REALY TECH" Rapid Coronavirus Antigen Test (SARS-Cov-2)
Product Description -
Specifications
Test duration: 15 minutes
Sample type: nasopharyngeal swab.
Storage: at room temperature or refrigerated (2-30A' C)
Expiration: 24 months ex works
Price of product ( USD price or FOB price) - DEPENDS ON QUANTITY
Product origin -
China
Key Specifications/Special Features -
5 test boxes: Each test box is packed in an aluminum foil bag with desiccant.
5 extraction reagents: vial with 0.3 ml extraction reagent
5 sterilized swabs: disposable swabs for sample collection
5 extraction tubes
5 dropper tips
1 work station
1 leaflet
Minimum Order Size and Packaging details -
MOQ 30000 units
Health Canada Authorised Rapid Test
The COVID-19 antigen rapid test device is a lateral flow in-vitro immunoassay intended to be used for the qualitative detection of the SARS-CoV-2 viral nucleoprotein. This device will detect both viable and nonviable virus in both nasopharyngeal and oropharyngeal secretions.
This test had been authorized for point of care use by Health Canada and is available for immediate dispatch
MediGuard Systems of Canada is an Authorised distributor of the Assuretech Rapid Antigen test.
Support documentation and details available on request
The HIV-1/2 Rapid Screen Test (RST) is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2(HIV-1/2) in human serum/plasma and whole blood. It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA.
Precaution
1.For in vitro diagnostic uses only.
2.All patient samples should be treated as if capable of transmitting diseases.
3.Do not use test kit beyond expiration date.
4.Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
Summary And Explanation Of The Test
It has been shown that the acquired immunodeficiency syndrome (AIDS) is caused by viruses transmitted by sexual contact, transfusion, use of contaminated blood products and sharing contaminated needles. HIV-1 and HIV-2 viruses have been isolated from patients with AIDS and AIDS-related complex (ARC), high-risk persons for AIDS. HIV-1 and HIV-2 viruses delete T helper cells, a subpopulation of T cells for body defense, thus causing AIDS patients susceptible to opportunistic infections and developing malignant tumors. The incidence of specific antibodies to HIV-1/2 is high in AIDS, ARC and persons with high risk for AIDS. The HIV-1/2 Rapid Screen Test is designed to detect antibodies to HIV-1/2 in AIDS patients, ARC or high risk persons and identify any potential donors carrying these antibodies in serum specimens.
Principle
HIV-1/2 RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum/plasma and whole blood. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, a red colored band will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen. Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.
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.
The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens.
Principle
The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests 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.
Storage and Stability
1.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.
2.The test must remain in the sealed pouch until use.
The mor gold rapid screen test strip is a fast and easy to read membrane chromatographic immunoassay with no need for instrument. The method employs a unique combination of monoclonal and polyclonal antibodies to specifically identify morphine in urine with a high degree of sensitivity.
Morphine, one of opiates derivatives, is central nervous system stimulants that produce alertness, wakefulness, increased energy, reduced hunger, and an overall feeling of well-being. Morphine has been the preferred drug for the management of pain in cases of advanced cancer and other severe conditions. Morphine and other opiates metabolites may be detected in urine as a result of heroin morphine, codeine, or poppy seed intake. Administration of large doses of morphine can cause tolerance and physiological dependence in users, and can lead to substance abuse. D-morphine is controlled substances. Gc/ms or immunoassay method has been developed for the determination of 300ng/ml for morphine.
Mor test principle
During a test labeled antibody-dye conjugate mixes with urine specimen and binds to the free drug if it is presented in the sample, to form an antibody-antigen complex. This complex prevents the formation of pink color bands in the test zone of the dip-stick if drug to be detected in specimen is above the detection levels (300ng/ml for morphine). In case of absent of drug and its metabolites, unbound dye conjugate will bind to the antigens immobilized in the test zone to form a pink reaction line. To serve as a quality control for the assay, another pink line will always appears in the test zone regardless positive or negative result.
The helicobacter-pylori antigen rapid test kit (stool) is a rapid visual immunoassay for the qualitative detection of helicobacter pylori antigen in human stool specimens. This kit is used as an aid in the diagnosis of h. Pylori infection.
Introduction
Helicobacter pylori (also known as campylobacter pylori) as a spiral-shaped gram negative bacteria which infects the gastric mucosa. H. Pylori to causes several gastro-enteric diseases such as non-ulcerous dyspepsia, gastric and duodenal ulcer, active gastritis and can even increase the risk of stomach adenocarcinoma.
The epidemiologic study shows that more than 50% of the world's population is infected by h. Pylori strains. Infection is more prevalent in developing countries. The lowest infection rate is 20%, and the highest infection rate can be 90% in developing countries. H. Pylori strains is the major reason to cause chronic gastritis and gastric ulcers, 80%-90% chronic gastritis patients and 95%-100% gastric ulcers patients are infected by h. Pylori strains. So the detection and treatment of h. Pylori strains infection is very important.
At present several invasive and non-invasive approaches are available to detect this infection state. Invasive methodologies require endoscopy of the gastric mucosa with histologic, cultural and urease investigation, which are expensive and require some time for diagnosis. Alternatively, non-invasive methods are available such as breath tests, which are extremely complicated and not highly selective, and classical elisa and immunoblot assays. This kit belongs to non-invasive approach.
Intended use
Canine distemper virus ag test is a sandwich lateral flow immunochromatographic assay for the qualitative
Detection of canine distemper virus (cdv ag) in dogs secretions or serum.
Assay time: 5-10 min
Sample: secretions or serum
Principle
Canine distemper virus ag test is based on sandwich lateral flow immunochromatographic assay. The test
Device has a testing window. The testing window has an invisible t (test) zone and c (control) zone. When
Sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test
Strip. If there is enough distemper antigen in the sample, a visible t band will appear. The c band should
Always appear after a sample is applied, indicating a valid result. By this means, the device can accurately
Indicate the presence of canine distemper antigen in the sample.
One-Step Canine Influenza Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine Influenza virus (CIV Ag) in dogs secretions.
Sensitivity: 94.7% , Specificity: 100%
Specimen: Secretions
Reading Timen:5-10 min
General Information
Method: Double Antibodies Sandwich Method
Sensitivity : 99.8%
Specificity : 99.6%
Specimen : Canine feces or vomit
Detection limit: 103 TCID50 / mL
No cross reaction against CDV, CCV, CRV, CAV - I, Giardia
Reading Time : 5- 10 min
One-Step the D-Dimer Rapid Test Device is a chromatographic immunoassay for the qualitative detection of D-Dimer in human blood.
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 -15min
General Information
One-Step FOB Rapid Test is qualitative test for the detection of human blood hemoglobin in human stool specimens and early diagnosis for Colon Cancer by Fecal Occult Blood screening with double methods, immunology and chemistry No Cross reactivity :(Bovine, Hemoglobin, Swine hemoglobin, Horse hemoglobin, Bililrubin, Bovine serum albumin, Vitamin C) Analytical sensitivity : 20ng/ml of FOB (immunology) ,100ng/ml of FOB (chemistry)
Specimen : Stool
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 Chagas IgG/IgM Rapid Test is detection of IgG anti-Trypanosoma cruzi (T. cruzi) in human blood.
Sensitivity: 92.9% , Specificity: 100%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 min
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
General Information
One-Step Dengue Rapid Test is to detect the NS1 antigens in serum, plasma or whole blood.
Sensitivity : 99.9% , Specificity : 99.5%
Specimen : Serum , Plasma and 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
General Information
One-Step H.Pylori Ab Rapid Test is to detect the antibodies against H. pylori in serum, plasma or whole blood.
For H.Pylori Ab Rapid tests:
Sensitivity: 98.9 %, Specificity: 98.5%,
Specimen: Serum, Plasma or Whole Blood
Reading Time: 10 min
General Information
One-Step H.Pylori Ag Rapid Test is to detect the antigens in stool.
For H.Pylori Ag Rapid tests:
Sensitivity: 98.9 %, Specificity: 98.5%,
Specimen: Stool
Reading Time: 10 min
General Information
One-Step Rotavirus Rapid Test (Feces) is a rapid visual immunoassay for the qualitative presumptive detection of rotavirus in human fecal specimens.
Sensitivity: 99.1% , Specificity: 99.9%
Detection limit:103.5TCID50/ml
Specimen: Feces
Reading Time : 10min
General Information
One-Step Adenovirus Rapid Test (Feces) is a rapid visual immunoassay for the qualitative presumptive detection of adenovirus in human fecal specimens.
Sensitivity: 98.7% , Specificity: 98.0%
Detection limit:1.37s/CO
Specimen: Feces
Reading Time : 10min
General Information
The CRP Semi-Quantitative Rapid Test utilizes a combination of colloidal gold conjugate and anti-CRP antibodies to selectively detect CRP in human blood.
Sensitivity:97% , Specificity:96.9%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 -15min
General Information
The CRP C-Reactive Protein Semi-Quantitative Rapid Test utilizes a combination of colloidal gold conjugate and anti-CRP antibodies to selectively detect CRP in human blood.
Sensitivity:97% , Specificity:96.9%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 -15min
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