Shanghai Sunland Industrial Co., Ltd is the top manufacturer of Personal Protect Equipment in China, with 20 years’experience. We are the Chinese government appointed manufacturer for government power,personal protection equipment , medical instruments,construction industry, etc. All the products get the CE, ANSI and related Industry Certificates. All our safety helmets use the top-quality raw material without any recycling material.
Medical grade II protective clothing is classified

We provide exclusive customization of the products logo, using advanced printing technology and technology, not suitable for fading, solid and firm, scratch-proof and anti-smashing, and suitable for various scenes such as construction, mining, warehouse, inspection, etc. Our goal is to satisfy your needs. Demand, do your best.
Professional team work and production line which can make nice quality in short time.
We abide by the privacy policy and human rights, follow the business order, do our utmost to provide you with a fair and secure trading environment, and look forward to your customers coming to cooperate with us, openly mind and trade with customers, promote common development, and work together for a win-win situation.
The professional team provides 24 * 7 after-sales service for you, which can help you solve any problems









Type: ,Medical, surgical ,sterilization equipment,. ,Sterilization, capacity: 2-20 cbm one time. Sterilant: Ethylene oxide ,sterilization, gas. Features: High efficiency, intelligent system, high safety. Application: Dispossable ,medical, mask, surgical masks, ,protective clothing,, ,medical equipment, and so on

Biomedomics' COVID-19 ,rapid, test ,kit,. -- BioMedomics photo Morrisville-based BioMedomics, a small diagnostics ,company, supported by the North Carolina Biotechnology Center, has developed a new test for rapidly detecting COVID-19, the coronavirus infection that is spreading rapidly throughout the world.. The ,company, is working overtime to deploy its COVID-19 IgM-IgG ,Rapid, Test, an immunoassay ...

Easy to use, high accuracy & reliable results. The COVID-19 IgG/IgM ,Rapid, Test Cassette is a lateral flow chromatographic immunoassay for the qualitative ,detection, of IgG and IgM antibodies to COVID-19 in human whole blood, serum or plasma specimen. Every pack contains 30 Biozek ,Rapid, Test COVID-19 ,Kits,, NCP=402, 2019-nCoV

Medline provides products and clinical solutions to all markets across the continuum of healthcare: hospitals, long-term care facilities, surgery centers, home …

9/4/2020, · The following day, the Department of Health in the Philippines authorized the use of the ,company,’s ,rapid, test ,kit, for the ,detection, of COVID-19. The EU gave its approval to market and sell the ...

Every ,rapid, test is manufactured under ISO 13485-2003 CMDCAS requirements for Medical Device License from Health Canada and FDA QSR. Our ,company, is dedicated to making sure you are satisfied with the ELISA test ,kit, you purchase.

Two gene lyophilized Covid-19 RT-PCR ,kits, are also available for markets which requirethose. The Anti-SARS-CoV-2 ,Rapid, Test ,Kit, is a lateral flow immunoassay intended for the qualitative ,detection, and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human plasma from anticoagulated blood (Heparin/ EDTA/ sodium citrate) or serum.

Detection, of COVID-19 (SARS-CoV-2) N-Protein IgM & IgG antibodies in human serum, whole blood, or finger prick samples. This product is for in-vitro diagnostic use, following guidance from the FDA for Emergency Use Authorization.

9/4/2020, · The following day, the Department of Health in the Philippines authorized the use of the ,company,’s ,rapid, test ,kit, for the ,detection, of COVID-19. The EU gave its approval to market and sell the ...

9/4/2020, · The ,kits, are designed differently by each producing ,company, and we will look at the producing ,companies, at the end of this discussion. But however the design, the working principle is the same. The test aims at detecting for the presence of IgG and/or IgM antibodies ,produced, during COVID-19 infection.

Homegrown technology ,company, Biogenes Technologies Sdn Bhd is developing an aptamer-based biosensor against the novel coronavirus that can accurately deliver test results in under one minute. The technology is the result of a collaboration between Biogenes and San Francisco-based start-up Pinpoint Science Ltd. The aim is to design and develop a DNA-based aptamer against the novel coronavirus ...

Company, Profile. Based in Belgium and established in 1996, Coris BioConcept is a middle-sized ,company, (SME) specialized in developing, manufacturing and marketing ,rapid, diagnostic ,kits, for the ,detection, of human respiratory and gastro-enteric infectious pathogens (bacteria, viruses and parasites) and for the ,detection, of antibiotic resistance markers (RESIST range).

23/7/2020, · NIPD Genetics Public ,Company, Limited: ... Ltd. SYNTHGENE COVID-19 IgM/IgG ,Rapid Detection Kit, ... is currently soliciting proposals for projects to rapidly ,produce, innovative SARS-CoV-2 …

6210103000. Product Description. Irradiation Sterilization Type Medical Protective Clothing (TP) Meets GB19082-2009 testing standard. Capacity is more than 500,000 units in March. Capacity is about 800,000 units in April. Minimum order quantity: 10,000 pieces.

4 Fast Covid-19 Test ,Kits, That Could Turn the Tide of the Pandemic By Sissi Cao • 03/19/20 1:04pm The U.S. has the lowest number of tests per million people among countries hit by Covid-19.

Seoul, South Korea--(Newsfile Corp. - April 8, 2020) - 'SGTi-flex COVID-19 IgM&IgG' is an immunochromatographic test ,kit, for the qualitative determination of COVID-19's IgM and IgG antibodies in whole blood (finger prick or venous), serum or plasma.

In YG Machinery, we have many protective equipment, such as a knapsack sprayer, mask making machine, glove making machine, disinfection door.

Detection, of COVID-19 (SARS-CoV-2) N-Protein IgM & IgG antibodies in human serum, whole blood, or finger prick samples. This product is for in-vitro diagnostic use, following guidance from the FDA for Emergency Use Authorization.