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

焯傑實業有限公司

Why chose us ? 1. Professional metal lapel pins manufacturer, with large production capacity. 2. Competitive prices, EXW factory prices. 3.100%inspectionbeforepacking;Spotinspectionbeforeshipment 4. All products are green products, eco-friendly 5. Always provide our best after sale service for all the overseas customers , and we accept OEM design and can do whatever you want .  Shipping:By DHL / FedEx / UPS / TNT / Sea / Air... 1.For small quantities, we suggest shipping by express door to door service as it is more favorable, fast and convenient 2.For bigger quantities, it can be shipped by air or sea.  How to custom Order 1. Send Inquiry. 2.Confirm fully details with you immediately, and then revert back withquotation. 3. Price approval, then offer design, delivery &amp; payment methods. 4. Send you Invoice for payment. 5. Sample production. 6. Sample photos taken from every angle for your approval OR deliver to you check personally. 7. Sample approved, mass production begin. 8. Package taken from every angle OR a 3rd party for inspection before delivery. 9. Arrange delivery once remain payment received. 10. Update you on delivery status until parcel arrived completely. 11. Your precious suggests &amp; advices regarding our service &amp; quality.  

HIV / AIDS Awareness Ribbon Pin Badge, Gold Ribbon Enamel Lapel Pin

HIV AIDS Awareness Ribbon Gold Ribbon Enamel Pin Badge

Redress Ltd

XAVAN

MGM Industries & Company

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)

The high-quality and health-graded screen protector has passed ISO 21702 tests against killing 99% of viruses in 30min.  Viruses include influenza H1N1, and human strains of coronavirus (COVID-19).  High efficacy of killing viruses within 30 minutes and bacteria within 10 minutes of physical contact with your device 

Anti-Virus Mobile Phone Screen Protector (Clear)

Anti Virus Mobile Phone Screen Protector Clear

COG Ltd

This virus cell model lets users see how viruses multiply and what it takes to stop them. The cross-sectional model gives extra educational value. 	 Detailed layers with removable parts. 	 Age Group: Ages 7 and up. 	 Package Dimensions: L: 9.2cm W: 10.5cm H: 9.2cm  

Bio Signs: Virus

Bio Signs: Virus - a detailed virus cell model

For early detection of COVID-19 infection 

ARISTA COVID-19 Antigen Rapid Test

POPABE LIMITED

東美實業有限公司

 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

VivaChek Biotech (Hangzhou) Co., Ltd.

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

Max Choice Corporation Limited

Features:Innovation based on AI-PPT global patented technologyAntico uses innovative AI-Pharmaceutical Platform Technology, which calculates the active ingredients and their effectiveness with precision through artificial intelligence, creates a navigational formula, and targets the root cause for rapid effectiveness.Function: Relieve various symptoms of Long COVID-19, including brain fog, fatigue, cough, excess phlegm, shortness of breath, body aches, insomnia, and other related symptoms.Ingredients: Cordyceps, Peruvian Black MacaActive ingredients: Cordyceps polysaccharides, cordycepin, maca alkaloids, macaenes, macamide.Packaging: 12 pills per box, each pill weighing 250 milligramsDosage: Twice a day, two pills each time, on an empty stomach (1 hour before or 2 hours after meals); half dosage for childrenStorage method: Store in a dry and cool place, avoid sunlight; or refrigerate in a refrigerator.Origin: Canada.*This product is not registered under the Pharmacy and Poisons Ordinance or the Chinese Medicine Ordinance. Any claim made for it has not been subject to evaluation for such registration. This product is not intended to diagnose, treat or prevent any disease.

dr. tam Antico Long Covid Formula 12's

dr tam Antico Long Covid Formula for Long COVID relief

The high-quality and health-graded screen protector has passed ISO 21702 tests against killing 99% of viruses in 30min.  Viruses include influenza H1N1, and human strains of coronavirus (covid-19).  High efficacy of killing viruses within 30 minutes and bacteria within 10 minutes of physical contact with your device 

Anti-Virus Protector Mask

Anti Virus Protector Mask with high efficacy against viruses

Anti-Virus Mobile Phone Screen Protector (Anti-Glare)

Anti Virus Mobile Phone Screen Protector with anti glare

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

 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

流行工坊有限公司

 	 Customized name&nbsp; 	 IP black 	 Total weight: 6 grams 	 Dimensions: 30 x 21.3 mm  

Covid-19 HERO Brooch / Pin

Changchun Wancheng Bio-Electron Co., Ltd.

HCG Test Kit

Synmax Vinyl Exam Gloves

Synmax Vinyl Exam Gloves for health protection and prevention.

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

WooriDo Co.,Ltd.

5C-B19

Fashion Farm Foundation Limited

YMDH

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. 

我的採購

確定要取消關注此供應商？

確定要取消關注此供應商？