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.
respirator mask 3d model

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








Consultation hotline:0086-15900663312
Email:sale@sunlandsafety.com
Address:No. 3888, Hutai Road, Baoshan District, Shanghai, China

Testing ,kits, and reagents for the ,detection, of SARS-CoV-2 in Swabs of Environmental Surfaces. SARS CoV-2 (,COVID-19,) is a recently discovered ,coronavirus,, which has caused the pandemic ,COVID-19, outbreak. This virus may lead to severe acute respiratory syndrome (SARS) and is predominantly transmitted person to person via droplets and possibly ...

A new, method to detect ,coronavirus, infections has been developed in the pre-print, The SARS-COV-2 spike protein binds sialic acids, and enables rapid ,detection, in a lateral flow point of care diagnostic device, published by researchers from the University of Warwick, University of Manchester and Iceni Diagnostics ltd based in Norwich.

SINGAPORE-BASED biotech firm Veredus Laboratories on Thursday said its ,coronavirus, test has received provisional authorisation from Singapore's Health Sciences Authority for in-vitro diagnostic use. This means the VereCoV ,detection kit, can now be used directly by laboratories or hospitals...

The ,new, virus ,detection, product, called Novel ,Coronavirus, (2019-nCoV) IgM/IgG antibody ,detection kit,, was developed by the century-old university based in northern China's Tianjin, with a group of ...

20/3/2020, · Gencurix Releasing ,New Coronavirus, Diagnostic ,Kit, in the EU PR Newswire SEOUL, South Korea, March 20, 2020 SEOUL, South Korea, March 20, 2020 /PRNewswire/ -- ,A new, diagnostic ,kit, for the ,COVID-19, ...

SINGAPORE-BASED biotech firm Veredus Laboratories on Thursday said its ,coronavirus, test has received provisional authorisation from Singapore's Health Sciences Authority for in-vitro diagnostic use. This means the VereCoV ,detection kit, can now be used directly by laboratories or hospitals...

The Novel ,Coronavirus, Antigen ,Detection Kit, (Colloidal Gold) is for the qualitative ,detection, of antigen of novel ,coronavirus, in human sputum or stool samples. It provides an aid in the diagnosis of infection with novel ,coronavirus,.

The ,new, Abbott ID NOW ,COVID-19, test runs on Abbott's ID NOW TM platform — a lightweight box (6.6 pounds and the size of a small toaster) that can sit in a variety of locations. Because of its small size, it can be used in more non-traditional places where people can have their results in a matter of minutes, bringing an alternate testing technology to combat the novel ,coronavirus,.

13/3/2020, · Tests ,kits, to be imported and sold by Kurabo Industries Ltd. are said to detect the ,new coronavirus, from a blood sample in 15 minutes. | KYODO National 15-minute ,coronavirus, test ,kits, to …

Coronavirus, (2019-nCoV) ,Detection Kit, is a real-time RT-PCR test intended for the qualitative ,detection, of SARS-CoV-2 nucleic acid extracted from nasopharyngeal swabs, oropharyngeal (throat) swabs ...

The Novel ,Coronavirus, Antigen ,Detection Kit, (Colloidal Gold) is for the qualitative ,detection, of antigen of novel ,coronavirus, in human sputum or stool samples. It provides an aid in the diagnosis of infection with novel ,coronavirus,.

13/3/2020, · Tests ,kits, to be imported and sold by Kurabo Industries Ltd. are said to detect the ,new coronavirus, from a blood sample in 15 minutes. | KYODO National 15-minute ,coronavirus, test ,kits, to …

Updated October 14, 2020. Latest information on products and support for laboratories studying SARS-CoV-2 in response to the ,coronavirus, (,COVID-19,) pandemic. Includes trending news, viral RNA extraction/isolation ,kits,, PCR products, viral reporters and cell viability assays supporting ,COVID-19, research and diagnostic test development.

A new, method to detect ,coronavirus, infections has been developed in the pre-print, The SARS-COV-2 spike protein binds sialic acids, and enables rapid ,detection, in a lateral flow point of care diagnostic device, published by researchers from the University of Warwick, University of Manchester and Iceni Diagnostics ltd based in Norwich.

2/9/2020, · Gencurix Releasing ,New Coronavirus, Diagnostic ,Kit, in the EU PR Newswire SEOUL, South Korea, March 20, 2020 SEOUL, South Korea, March 20, 2020 /PRNewswire/ -- ,A new, diagnostic ,kit, for the ,COVID-19, ...

13/4/2020, · Shimadzu Corporation is announcing the release of its “2019 Novel ,Coronavirus Detection Kit,”, with sales beginning on 20th April. For the time being the ,kits, will only be available in Japan, but preparations are underway to export these ,kits, overseas from May onwards.

In early 2020, CDC developed its first laboratory test ,kit, for use in testing patient specimens for SARS-CoV-2. The test ,kit, is called the CDC 2019 Novel ,Coronavirus, (2019-nCoV) Real-Time Reverse Transcriptase (RT)–PCR Diagnostic Panel.. On February 3, 2020, CDC submitted an EUA package to expedite FDA-permitted use of the CDC diagnostic panel in the United States.