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  • SARS-CoV-2 Antigen kit1
  • SARS-CoV-2 Antigen kit
  • SARS-CoV-2 IgGIgM Rapid Test
You can check the list on the UK Department of Health website : https://www.gov.uk/.../medical-devices-regulations-2002... If you need to purchase our products, you can contact us at any time!

Lihlahisoa tsa rona li kene lethathamong la UK la lisebelisoa tsa tlhahlobo ea invitro tse sa lefelloeng!

O ka sheba lenane lena websaeteng ya Lefapha la Bophelo la UK : https://www.gov.uk/.../medical-devices-regulations-2002... Haeba o hloka ho reka dihlahiswa tsa rona, o ka ikopanya le rona ho nako efe kapa efe!
SHEBELLA EKETSEHILENG
SARS-CoV-2 has now evolved several mutations with serious consequences，some like B.1.1.7，B.1.351，B.1.2，B.1.1.28，B.1.617，Including the omicron mutant strain(B1.1.529) reported in recent days. As an IVD reagent manufacturer, we always pay attention to the development of relevant events, check the changes of relevant amino acids and evaluate the possible impact of mutations on reagents.

Tlaleho ea Teko le Tlhahlobong ea Silico bakeng sa Teko e potlakileng ea StrongStep® SARS-CoV-2 Antigen Rapid ho Mofuta o fapaneng oa SARS-CoV-2

SARS-CoV-2 e se e fetohile liphetoho tse 'maloa tse nang le litlamorao tse tebileng, tse ling tse kang B.1.1.7,B.1.351,B.1.2,B.1.1.28,B.1.617,Ho kenyeletsoa mofuta oa omicron mutant (B1.1.529) e tlalehiloe matsatsing a morao tjena.Joaloka moetsi oa reagent ea IVD, re lula re ela hloko nts'etsopele ea liketsahalo tse amehang, ho lekola liphetoho tsa li-amino acid tse amehang le ho lekola phello e ka bang teng ea liphetoho ho li-reagents.
SHEBELLA EKETSEHILENG
StrongStep® SARS-CoV-2 Antigen Rapid Test Enter the EU common list of hygiene and food safety, which is one of the few manufacturers that has 100% sensitivity when the CT value is less than 25%.

StrongStep® SARS-CoV-2 Antigen Rapid Test Kenya lenane le tloaelehileng la EU la bohloeki le polokeho ea lijo.

StrongStep® SARS-CoV-2 Antigen Rapid Test Kena lethathamong le tloaelehileng la EU la bohloeki le polokeho ea lijo, e leng e mong oa bahlahisi ba 'maloa ba nang le kutlo ea 100% ha boleng ba CT bo le ka tlase ho 25%.
SHEBELLA EKETSEHILENG
StrongStep® SARS-CoV-2 Antigen Rapid Test ncluded in the FIND evaluation list. The Foundation for Innovative New Diagnostics (FIND), is an organization that specializes in evaluating the performance of kits in strategic cooperation with WHO.

StrongStep® SARS-CoV-2 Antigen Rapid Test e kenyellelitsoe lenaneng la tlhahlobo ea FIND.

StrongStep® SARS-CoV-2 Antigen Rapid Test e kenyellelitsoeng lenaneng la litlhahlobo tsa FIND.The Foundation for Innovative New Diagnostics (FIND), ke mokhatlo o sebetsanang ka ho khetheha le ho lekola tšebetso ea lisebelisoa ka tšebelisano-'moho le WHO.
SHEBELLA EKETSEHILENG
Sequence alignment analysis showed that the mutation site of the SARS-CoV-2 variant observed in the in the United Kingdom , South Africa and India are all not in the design region of the primer and probe at present. StrongStep® Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit (detection for three genes) can cover and detect mutant strains ( shown in the following table) without affecting the performance at present. Because there is no change in the region of the detection sequence.

Polelo ka livaerase tse fapaneng

Tlhahlobo ea tatelano ea tatellano e bonts'itse hore sebaka sa phetoho sa mofuta oa SARS-CoV-2 se bonoang United Kingdom, Afrika Boroa le India kaofela ha li sebakeng sa meralo ea pele le lipatlisiso hajoale.StrongStep® Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit (ho lemoha liphatsa tsa lefutso tse tharo) e ka koahela le ho bona mefuta e fetotsoeng (e bontšitsoeng tafoleng e latelang) ntle le ho ama ts'ebetso ha joale.Hobane ha ho na phetoho sebakeng sa tatellano ea ho lemoha.
SHEBELLA EKETSEHILENG
We have received many certificate or EUA from different countries, such as United Kingdom, Singapore, Brazil, South Africa, Malaysia,Indonesia,Philippine, Argentine, Guatemala and so on. Also, we have send our products to many institue for evaluation, below are the summary of some data. Please contact us via guangming@limingbio.com if you need full artical of following report.

Kakaretso ea Tlaleho ea Tlhahlobo ho tsoa Setsing se fapaneng ka StrongStep® SARS-CoV-2 Antigen Rapid Test

We have received many certificate or EUA from different countries, such as United Kingdom, Singapore, Brazil, South Africa, Malaysia,Indonesia,Philippine, Argentine, Guatemala and so on. Also, we have send our products to many institue for evaluation, below are the summary of some data. Please contact us via guangming@limingbio.com if you need full artical of following report.
SHEBELLA EKETSEHILENG
Recently, the StrongStep® SARS-CoV-2 Antigen Rapid Test produced by Nanjing Liming Bio-products Co. Ltd has successfully obtained the Thailand FDA certificate (registration number T 6400429,T 6400430,T 6400431,T 6400432 ), and now has been approved to enter the Thailand market.

Thailand FDA COVID 19 ATK 2021 T6400429

Haufinyane tjena, StrongStep® SARS-CoV-2 Antigen Rapid Test e hlahisoang ke Nanjing Liming Bio-products Co. Ltd e atlehile ho fumana setifikeiti sa Thailand FDA (nomoro ea ngoliso T 6400429,T 6400430,T 6400431,T 6400432), 'me joale e se e le teng. e lumelletsoe ho kena 'marakeng oa Thailand.
SHEBELLA EKETSEHILENG
Recently, Nanjing LimingBio‘s Novel Coronavirus (SARS-CoV-2) antigen detection reagent

StrongStep® SARS-CoV-2 Antigen Rapid Test e fumane netefatso ea tšebetso ea Paul-Ehrlich-Institut (PEI) Jeremane!

Haufinyane tjena, "StrongStep® SARS-CoV-2 Antigen Rapid Test" ea Nanjing LimingBio's Novel Coronavirus (SARS-CoV-2) e fumane netefatso ea ts'ebetso ea Paul-Ehrlich-Institut (PEI*) Jeremane, sehlahisoa sena se entsoe. e netefalitsoeng ke Setsi sa Jeremane sa Federal for Medicines and Medical Device Administration (BfArM).LimingBio e fetohile e mong oa bahlahisi ba 'maloa Chaena ba fumaneng mangolo a mabeli a BfArM+PEI Jeremane.Teko e potlakileng ea antigen ea Liming Bio e fetisitse setifikeiti se nang le matla sa Lekala la Bophelo la linaha tse ngata, se pakang ka botlalo ts'ebetso e ntle ea kit.
SHEBELLA EKETSEHILENG
StrongStep® SARS-CoV-2 Antigen Rapid Test is a rapid immunochromatographic assay for the detection of COVID-19 antigen to SARS-CoV-2 virus in human Throat/Nasopharyngeal swab.

Teko e Potlakileng ea Antigen ea SARS-CoV-2

StrongStep® SARS-CoV-2 Antigen Rapid Test ke tlhahlobo e potlakileng ea immunochromatographic bakeng sa ho sibolla antigen ea COVID-19 ho vaerase ea SARS-CoV-2 ho human Throat/Nasopharyngeal swab.
SHEBELLA EKETSEHILENG
This highly sensitive, ready-to-use PCR kit is available in lyophilized format (freeze-drying process) for long-term storage. The kit can be transported and stored at room temperature and is stable for one year.

Novel Coronavirus (SARS-CoV-2) Multiplex Real-Nako PCR Kit

PCR kit ena e hlokolosi haholo, e seng e loketse ho sebelisoa e fumaneha ka mokhoa oa lyophilized (mokhoa oa ho omisa ka leqhoa) bakeng sa polokelo ea nako e telele.Thepa e ka tsamaisoa le ho bolokoa mocheso oa kamore 'me e tsitsitse selemo se le seng.
SHEBELLA EKETSEHILENG

LIHLAHISO TSA RONA

HAPE
about us

MABAPI LE RONA

Nanjing Liming Bio-products Co., Ltd. e thehiloe ka 2001, k'hamphani ea rona e khethehile ho nts'etsapele, ho etsa le ho rekisa liteko tse potlakileng tsa mafu a tšoaetsanoang haholo-holo mafu a likobo.Ntle le ISO13485, hoo e batlang e le lihlahisoa tsohle tsa rona li tšoailoe 'me CFDA e amohetsoe.Lihlahisoa tsa rona li bonts'itse ts'ebetso e ts'oanang ha e bapisoa le mekhoa e meng (ho kenyeletsoa PCR kapa setso) e jang nako ebile e bitsa chelete e ngata.Ka ho sebelisa liteko tsa rona tse potlakileng, lingaka kapa litsebi tsa tlhokomelo ea bophelo li ka boloka nako e ngata ea ho leta hobane e hloka metsotso e 10 feela.

HAPE
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Teko ea Motho ea Coronavirus Igm/Igg Antibody, Antibody Test Kit, Coronavirus Bakeng sa Teko ea Covid-19, Novel Coronavirus 2019 Ncov, Tlhahlobo ea Cryptococcal Antigen, Covid-19 Rapid Test Kit,
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