Tomax Industries Ltd

 COVID-19 IgG/IgM Rapid Test &amp; SARS-CoV-2 Proteins 

Serological immunoassay is an important auxiliary method for the diagnosis of COVID-19. The combination with molecular diagnostic is helpful to improve the accuracy of COVID-19 detection.&nbsp;
-&nbsp;Result available in 10-15 minutes.
- Whole blood, serum and Easy storage, 4-30&deg;C.

The colloidal gold immunoassay (CGIA) to detect COVID-19 utilizes the specific reaction between anti gen and antibody to detect the anti-SARS-CoV-2 antibody in patients&#39; sample. The advantages of CGIA is fast and convenient, stable sample collection, high throughput, and the result can be interpreted by naked eye.

 Product Features: 
COVID-19 IgM: 167 clinical specimens from individuals suspected of COVID-19 infection were detected by COVID-19 IgG/IgM rapid test cassette of CLONGENE&reg;, The result was compared with that of RT-PCR.

 Reproducibility: 
0 clinical serum specimens include 20 negative, 20 borderline positive and 20 posi- tive were tested in three physician office laboratories (POL), and each specimen was tested for three days at each POL. The intra-assay agreements and the in- ter-site agreement was both 100%.

 Specificity: 
- No cross reactivity was observed with specimens from patients infected with HIV, HAV, HBSAG, HCV, TP, HTLV, CMV, FLUA, FLUB, RSV, MP, CP, HPIVs.
-&nbsp;Common serum components, such as albumin, bilirubin, hemoglobin, et. al., do not Interfere with the COVID-19 IgG/IgM rapid test cassette of CLONGENEⓇ
- No cross reactivity or interference was observed with common biological analytes.

COVID-19 Rapid Test

COVID 19 Rapid Test for quick and accurate detection

MGM Industries & Company

Easy-to-use nasal swab test Requires just 1 test* Can be used to test children as young as 2 years old For use with and without COVID-19 symptoms Accurate results in 15 minutes No need to send off to a lab to obtain results Compact packaging for “On-The-Go” testing *Other COVID-19 antigen home tests may require a 2nd test 2-3 days after the first.  This product has not been FDA cleared or approved but has been authorized by FDA under an EUA.  This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens.  The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of IVDs for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated, or authorization is revoked sooner. 

COVID-19 Antigen Home Test

COVID 19 Antigen Home Test for quick and easy results

The iHealth® COVID-19 Antigen Rapid Test is a lateral flow assay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2.  This test is authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 15 years or older with symptoms of COVID-19 within the first 7 days of symptom onset. This test is also authorized for non-prescription home use with adult-collected nasal swab samples from individuals aged 2 years or older with symptoms of COVID-19 within the first 7 days of symptom onset.  This test is also authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 15 years or older, or adult collected anterior nasal swab samples from individuals aged 2 years or older, with or without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over three days with at least 24 hours (and no more than 48 hours) between tests.  This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA; This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens; and, The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.  Disclaimer: If you’re currently experiencing COVID-19 symptoms, please contact your primary care physician (PCP) for immediate guidance. iHealth® COVID-19 Antigen Rapid Test may take several days to ship. This is not a PCR test and not valid for travel. The manufacturer of the iHealth® COVID-19 Antigen Rapid Test requires test kits be stored at temperatures between 36o and 86oF (2o - 30oC). Any extended exposure of the test kit to temperatures beyond this range may affect quality of test results. If you have ordered home delivery of the test kit and expect temperatures in your area to be outside of this range at time of delivery, it is recommended that you arrange for someone to be home at or near time of delivery to receive the test kit. 

 COVID-19 Antigen Rapid Test Self-Test at Home

COVID 19 Antigen Rapid Test for self-testing at home

For early detection of COVID-19 infection 

ARISTA COVID-19 Antigen Rapid Test

 COVID-19 Antigen Rapid Test Cassette (Swab) 
Designed for qualitative detection of SARS-CoV-2 antigen in Swabs

 SARS-CoV-2 Nucleocapsid Protein Detection 
Nucleocapsid [N] protein is the most abundant protein with highly conserved in SARS Cov 2. N protein is used as the core raw material of rapid diagnostic reagent for immunalogy in the market.

 COVID-19 Antigen Rapid Test Cassette 
We has developed the COVID-19 Antigen Rapid Test Cassette. The colloidal gald immunoassay (CGIA) to detect nucleacapsid protein of SARS-CoV-2 is based on the principle of the double antibody -sandwich technique.

The combination of COVID-19 Antigen Rapid Test and COVID-19 IgG/IgM Rapid Test can improve the accuracy of SARS-CoV-2 (COVID-19) detection. We also can provide the COVID-19 IgG/IgM Rapid Test Cassette. Please contact us for more information.

COVID-19 Antigen Rapid Test Cassette (Swab)

COVID 19 Antigen Rapid Test Cassette Swab

Medomics SARS-CoV-2 Antigen Test Kit (LFIA) is used for in vitro detection of SARS-CoV-2 in nasopharyngeal swab, throat swab, nasal swab samples. ● Packing size: 20 tests/kit ● Specimen type: Nasal swabs, Throat swabs, BALF ● Instrumentation: not required ● Detection time: 15-20 minutes ● Storage: Room temperature (2-30°C) ● Shelf life: 24 months 

SARS-CoV-2 Antigen Test Kit (LFIA)

VivaChek Biotech (Hangzhou) Co., Ltd.

FOB (Fecal Occult Blood) serves as an early warning sign for colorectal cancer and other gastrointestinal diseases. A sample of approximately 50mg, collected from at least 5 different parts of the stool, is required for testing. Each year, over one million patients worldwide suffer from gastrointestinal bleeding and need early screening.  The VivaDiag FOB Rapid Test Strip adopts the colloidal gold method, delivering results in 10 minutes. For professional use by healthcare workers only, it facilitates early screening and diagnosis of gastrointestinal diseases. 

VivaDiag FOB Rapid Test

VivaDiag FOB Rapid Test for early screening of gastrointestinal diseases

Smart Idea Health Technology Ltd

World-First Rapid Test for Early Dementia RiskAD Check認知測™ Rapid utilizes world-leading patented technology to detect Amyloid β-protein fragments in urine—a key biomarker associated with dementia—to assist in screening potential cognitive risks. Designed as a rapid diagnostic kit, the test requires only a small urine sample and delivers results with 10 minutes. This non-invasive, streamlined, and highly efficient workflow makes it an ideal tool for both preliminary screenings and long-term health monitoring. By identifying risk signals early, users can strategically plan targeted medical follow-ups and professional diagnostics, ensuring critical intervention during the " golden intervention period." The technology has earned extensive international recognition, including the CE certification (EU) and medical device registrations across China and Southeast Asia. It holds invention patents in major jurisdictions, including China, Europe, Japan, and Australia. Clinical studies comparing AD Check™ Rapid with Aβ-PET imaging demonstrate high diagnostic performance, with sensitivity and specificity reaching approximately 80% and 90%, respectively  

AD Check 認知測™ Rapid-One Step Dementia Risk Test Kit

AD Check Rapid One Step Dementia Risk Test Kit

For the qualitative assessment of IgG/IgM antibody in human serum, plasma or whole blood. For professional In Vitro Diagnostic Use Only.Sample type: serum, plasma, venous whole blood.Sample: whole blood 20uL;serum / plasma 10uL.Interpretation of results: 15 minutes to interpret the results. 

IgM/IgG Antibody Test Kit

IgM IgG Antibody Test Kit for qualitative assessment

Changchun Wancheng Bio-Electron Co., Ltd.

HCG Test Kit

VivaDiag Strep A Test Kit (FIA) is a fluorescence immunoassay (FIA) for the qualitative detection of strep A in human throat swab samples. It is useful as aid in the diagnosis of Group A Streptococcal infection. Forin vitrodiagnostic use only.For professional use only. 

VivaDiag Strep A Test Kit (FIA)

VivaDiag Strep A Test Kit FIA for strep A detection

Fentanyl is a synthetic opioid 50–100 times more potent than morphine, and just 2 mg can be fatal. Each year, around 300,000 people worldwide die from drug overdoses, including approximately 125,000 opioid-related deaths. Rapid and precise diagnostics are crucial for effective management and control of drug abuse. Our Solution – First handheld CLIA Waived &amp; OTC Approved FIA Reader!!! Revolutionize fentanyl detection with the innovative BioSieve™ Toxismart™ Fluorescence (FIA) Reader, paired with the BioSieve™ Fentanyl FIA Pro Test Kit. This advanced system offers exceptional accuracy and efficiency, utilizing cutting-edge fluorescence technology to detect fentanyl in human urine at ultra-low concentrations of 1 ng/mL. 

BioSieve™ Toxismart™ Fluorescence (FIA) Reader

BioSieve Toxismart Fluorescence FIA Reader for fentanyl detection

Urine Test Strips 10 Parameters

Introduction: The chemiluminescence immunoassay system uses magnetic particle separation technology, which uses magnetic particles as antibody carriers, which can be evenly distributed in the liquid phase reaction system, with faster reaction speed and higher efficiency. Using enzymatic chemiluminescence method, the light signal is more stable. A new generation of enzymatic substrates, with higher sensitivity and faster luminescence. Compared with the international brands, the chemiluminescence immunoassay reagents have good consistency. the coincidence reate can reach more than 95%, and the detection precision can reach CV&lt;2%   

Automatic Chemiluminescence Immunoassay

Automatic Chemiluminescence Immunoassay with high sensitivity and stability

Features: * Whole block scanning and formulated line scanning mode, 96-well double-color scanning takes only 5.5s * 6 channels fluorescence detection, no cross talk between different channels. * Unique bottom detection, compatible to reaction volume down to 5µl * New automatic hot lid, automatic open and close which is prevent reagent evaporation * LED excitation light source with super long service life * New TE module with special technique to ensure long service life * Available for a varienty of scientific research and clinical applications.    

Fluorescent Quantitative PCR Detection System

GuangZhou Supbio Bio-technology and science Co.,Ltd

Guangzhou Supbio Bio-Technology and Science Co., Ltd. proudly introduces its independently developed HIV-1 DNA Detection Kit (qPCR) — the world’s first approved IVD kit for HIV-1 DNA load quantification. This breakthrough product overcomes a long-standing global technical bottleneck: the inability of traditional PCR methods to reliably detect and quantify HIV-1 DNA. By achieving exceptional sensitivity and specificity simultaneously, Supbio’s innovative technology enables accurate quantification of HIV-1 DNA in human blood, setting a new benchmark for molecular HIV diagnostics. 

Human Immunodeficiency Virus Type 1 (HIV-1) DNA Detection Kit (Probe-based Quantitative PCR (qPCR))

HIV 1 DNA Detection Kit for quantitative PCR

Urine Test Strips 14 Parameters

Features: 1. Laser scatter technology. 2. Constant linear sheath flow. 3. 3-D topographic technology. 4. Auto loader, 60 samples/hour. 5. Integral titanium incubation system. 6. 28 parameters, 2 histograms, 2 scattergrams. 7. Random direction tube barcode scanning technology (optional).   

5 Part Auto Hematology Analyzer

Features: 1. Automatic electric potential tracking and correcting software to ensure the stable performance. 2. Automatically detect and filter tiny bubbles to avoid clog and ensure accurate measurement. 3. Real time diagnostic of system working status. 4. Waste liquid automatic detection and alarming. 5. Automatic calibration and two point correction to adjust slope and intercept. 6. Wave flushing method and direct flushing pipe method to avoid block and crossed contamination. 7. Power failure protection for data storage up to 10000 results. 8. Minimum consumption, reduce consumable cost. 9. Rapid test speed of 80 tests per hour.   

Auto Electrolyte Analyzer

Auto Electrolyte Analyzer with automatic calibration and rapid test speed

Chongqing Nanfang Numerical Control Equipment Co., Ltd.

Fully Automatic Agglutination Analyzer: Syphilis Screening 

Fully Automatic Agglutination Analyzer

Fully Automatic Agglutination Analyzer for syphilis screening

VivaChek Pro is a multi-function monitoring system with connectivity designed for hospital use. It features user authentication，Wifi/LAN data transmission，and integration with hospital systems (HIS/LIS/EMR). The device has a color touch screen, IR scanner and a strip ejector, making it easy to use and navigate. The meter can test glucose, ketone, uric acid, hemoglobin, total cholesterol, and lactate levels with great accuracy and reliability. Whether you're a doctor, a nurse, or a healthcare administrator, the VivaChek Pro Hospital Multi-function Monitoring System can significantly improve work efficiency and patient outcomes. 

VivaChek Pro Hospital Multi-function Monitoring System

VivaChek Pro Hospital Multi function Monitoring System

Features: 1. Easy operation by one button. 2. End point, kinetic, fixed time, rate, etc. 3. Filter wavelength: 340/405/450/510/546/578/630nm, 2 more open filter positions, others on request. 4. With 20 incubating positions. 5. Large Memory to store 144 test programs and 5600 testing results. 6. Excellent Q.C function, Q.C chat can be stored, displayed and printed. 7. 37ºC temperature in flow cell and incubating. 8. Real time graph can be displayed and printed.   

Semi -auto Chemistry Analyzer BIOBASE-Silver

Semi auto Chemistry Analyzer BIOBASE Silver

Application: Gel card centrifuge is used in blood serology, blood type coutine test, erythrocyte washing, microcolumn agglutination, immunology and other tests.  Features: * DC Brushless motor, low noise. * Microprocessor control system &amp; soft touch control panel. * LCD display: RCF, Speed, Time. * Electric lid interlock, over speed and imbalance protection. * 20 programs for standard and programmability are available.   

Gel Card Centrifuge

Gel Card Centrifuge for blood serology and testing

Application: Gel card centrifuge is used in blood serology, blood type routine test, erythrocyte washing, microcolumn agglutination, immunology and other tests.  Features: * DC Brushless motor, low noise. * Microprocessor control system &amp; soft touch control panel. * LCD display: RCF, Speed, Time. * Electric lid interlock, over speed and imbalance protection. * 20 programs for standard and programmability are available.  

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