• 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!

Zogulitsa zathu zalowa pamndandanda waku UK wa zida zodziwira ma invitro osatulutsidwa!

Mukhoza kuyang'ana mndandanda pa webusaiti ya UK Department of Health : https://www.gov.uk/.../medical-devices-regulations-2002... Ngati mukufuna kugula katundu wathu, mungatitumize pa nthawi iliyonse!
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.

Report Testing and in Silico Analysis for StrongStep® SARS-CoV-2 Antigen Rapid Test pa Zosiyana za SARS-CoV-2 Zosiyana

SARS-CoV-2 tsopano yasintha masinthidwe angapo okhala ndi zotulukapo zowopsa, zina ngati B.1.1.7,B.1.351,B.1.2,B.1.1.28,B.1.617,Kuphatikiza mtundu wa omicron mutant (B1.1.529) zafotokozedwa m'masiku aposachedwa.Monga opanga IVD reagent, nthawi zonse timayang'ana pakukula kwa zochitika zoyenera, kuyang'ana kusintha kwa ma amino acid oyenera ndikuwunika momwe kusintha kungakhudzire ma reagents.
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 Lowani pamndandanda wamba wa EU waukhondo ndi chitetezo chazakudya

StrongStep® SARS-CoV-2 Antigen Rapid Test Lowani pamndandanda wamba wa EU waukhondo ndi chitetezo chazakudya, womwe ndi m'modzi mwa opanga ochepa omwe ali ndi chidwi ndi 100% pomwe mtengo wa CT ndi wochepera 25%.
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 ikuphatikizidwa pamndandanda wowunika wa FIND

StrongStep® SARS-CoV-2 Antigen Rapid Test yophatikizidwa pamndandanda wowunika wa FIND.The Foundation for Innovative New Diagnostics (FIND), ndi bungwe lomwe limagwira ntchito yowunika momwe zida zimagwirira ntchito mogwirizana ndi WHO.
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.

Chidziwitso cha ma virus osiyanasiyana

Kusanthula kwamachitidwe kumawonetsa kuti malo osinthika amtundu wa SARS-CoV-2 omwe amawonedwa ku United Kingdom, South Africa ndi India onse sali m'chigawo choyambira komanso kufufuza pakadali pano.StrongStep® Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit (kuzindikira majini atatu) imatha kuphimba ndikuzindikira mitundu yosinthika (yosonyezedwa patebulo lotsatirali) popanda kusokoneza magwiridwe antchito pakadali pano.Chifukwa palibe kusintha m'chigawo cha mndandanda wodziwika.
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.

Chidule cha Lipoti la Evaluation kuchokera ku Different Institute pa 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.
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

Posachedwapa, StrongStep® SARS-CoV-2 Antigen Rapid Test yopangidwa ndi Nanjing Liming Bio-products Co. Ltd yapeza bwino chiphaso cha Thailand FDA (nambala yolembetsa T 6400429,T 6400430,T 6400431,T 6400432), ndipo tsopano yapezeka. adaloledwa kulowa mumsika wa Thailand.
Recently, Nanjing LimingBio‘s Novel Coronavirus (SARS-CoV-2) antigen detection reagent

StrongStep® SARS-CoV-2 Antigen Rapid Test yapeza chitsimikiziro cha magwiridwe antchito a Paul-Ehrlich-Institut (PEI) ku Germany!

Posachedwapa, Nanjing LimingBio's Novel Coronavirus (SARS-CoV-2) antigen reagent "StrongStep® SARS-CoV-2 Antigen Rapid Test" yapeza chitsimikiziro cha magwiridwe antchito a Paul-Ehrlich-Institut (PEI*) ku Germany. zovomerezeka ndi German Federal Agency for Medicines and Medical Device Administration (BfArM).LimingBio yakhala m'modzi mwa opanga ochepa ku China omwe adapeza ziphaso ziwiri za BfArM+PEI ku Germany.Kuyesa kwachangu kwa antigen kwa Liming Bio kwadutsa chiphaso chovomerezeka cha Unduna wa Zaumoyo m'maiko ambiri, zomwe zimatsimikizira magwiridwe antchito abwino kwambiri a zida.
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.

SARS-CoV-2 Antigen Rapid Test

StrongStep® SARS-CoV-2 Antigen Rapid Test ndi kuyesa kwachangu kwa immunochromatographic pozindikira COVID-19 antigen ku kachilombo ka SARS-CoV-2 pakhungu lamunthu / Nasopharyngeal swab.
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-Time PCR Kit

Zida za PCR zomverera kwambiri, zokonzeka kugwiritsa ntchito zimapezeka mumtundu wa lyophilized (njira yowumitsa zowuma) kuti zisungidwe kwa nthawi yayitali.Chombocho chikhoza kunyamulidwa ndikusungidwa kutentha kwa chipinda ndipo chimakhala chokhazikika kwa chaka chimodzi.

ZOPHUNZITSA ZATHU ZOTSOGOLERA

ZAMBIRI ZAIFE

Nanjing Liming Bio-products Co., Ltd. yomwe idakhazikitsidwa mu 2001, kampani yathu yakhala yapadera pakukulitsa, kupanga ndi kutsatsa mayeso othamanga a matenda opatsirana makamaka matenda opatsirana pogonana.Kupatula ISO13485, pafupifupi mankhwala athu onse ndi CE chizindikiro ndi CFDA ovomerezeka.Zogulitsa zathu zawonetsa magwiridwe antchito ofanana poyerekeza ndi njira zina (kuphatikiza PCR kapena chikhalidwe) zomwe zimatenga nthawi komanso zokwera mtengo.Pogwiritsa ntchito mayeso athu othamanga, odwala kapena akatswiri azachipatala amatha kupulumutsa nthawi yodikirira chifukwa zimangofunika mphindi 10.

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