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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!

Iimveliso zethu zingene kuluhlu lwase-UK lwezixhobo zokuxilonga ze-coronavirus ezikhululwe kwi-invitro!

Ungajonga uluhlu kwiwebhusayithi yeSebe lezeMpilo lase-UK: https://www.gov.uk/.../medical-devices-regulations-2002... Ukuba ufuna ukuthenga iimveliso zethu, ungaqhagamshelana nathi nangaliphi na ixesha!
BONA OKUNGAKUMBI
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.

Ingxelo yoVavanyo kunye noVavanyo lwe-Silico lwe-StrongStep® SARS-CoV-2 Antigen Rapid Test kwi-SARS-CoV-2 eyahlukileyo eyahlukileyo

I-SARS-CoV-2 ngoku iye yavela kwiinguqu ezininzi ezineziphumo ezibi, ezinye ezifana ne-B.1.1.7, B.1.351, B.1.2, B.1.1.28, B.1.617, Kubandakanya uhlobo lwe-omicron mutant (B1.1.529) ingxelo kwiintsuku zamva nje.Njengomenzi we-reagent ye-IVD, sihlala siqwalasela ukuphuhliswa kweziganeko ezifanelekileyo, sijonge utshintsho lwee-amino acids ezifanelekileyo kwaye sivavanye impembelelo enokwenzeka yokuguqulwa kwee-reagents.
BONA OKUNGAKUMBI
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%.

I-StrongStep® SARS-CoV-2 Antigen Rapid Test Ngena kuluhlu oluqhelekileyo lwe-EU lococeko kunye nokhuseleko lokutya

I-StrongStep® SARS-CoV-2 Antigen Rapid Test Ngena kuluhlu oluqhelekileyo lwe-EU lococeko kunye nokhuseleko lokutya, ongomnye wabavelisi abambalwa abanovakalelo lwe-100% xa ixabiso le-CT lingaphantsi kwama-25%.
BONA OKUNGAKUMBI
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.

IStrongStep® SARS-CoV-2 Antigen Rapid Test ibandakanyiwe kuluhlu lovavanyo lwe-FINDA

IStrongStep® SARS-CoV-2 Antigen Rapid Test ibandakanywe kuluhlu lovavanyo lwe-FINDA.I-Foundation for Innovative New Diagnostics (FIND), ngumbutho ogxile ekuvavanyeni ukusebenza kweekiti kwintsebenziswano yeqhinga kunye ne-WHO.
BONA OKUNGAKUMBI
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.

Ingxelo ngeentsholongwane ezahlukeneyo

Uhlalutyo lolungelelwaniso lolandelelwano lubonise ukuba indawo yoguqulo ye-SARS-CoV-2 eyahlukileyo ebonwe e-United Kingdom, eMzantsi Afrika nase-Indiya zonke azikho kummandla woyilo we-primer kunye nophando ngoku.I-StrongStep® Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit (ukubona imizila yemfuza emithathu) inokugquma kwaye ibone iintlobo eziguqukayo (eziboniswe kolu luhlu lulandelayo) ngaphandle kokuchaphazela ukusebenza ngoku.Ngenxa yokuba akukho tshintsho kummandla wokulandelelana kokufumanisa.
BONA OKUNGAKUMBI
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.

Isishwankathelo seNgxelo yoVavanyo evela kwiziko elahlukileyo kwi-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.
BONA OKUNGAKUMBI
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

Kutshanje, iStrongStep® SARS-CoV-2 Antigen Rapid Test eveliswe yiNanjing Liming Bio-products Co. Ltd ifumene ngempumelelo isatifikethi se-FDA yaseThailand (inombolo yobhaliso T 6400429, T 6400430, T 6400431, T 6400432 ), kwaye ngoku sele ikhona. ivunyiwe ukungena kwimarike yaseThailand.
BONA OKUNGAKUMBI
Recently, Nanjing LimingBio‘s Novel Coronavirus (SARS-CoV-2) antigen detection reagent

IStrongStep® SARS-CoV-2 Antigen Rapid Test ifumene isiqinisekiso sokusebenza se-Paul-Ehrlich-Institut (PEI) eJamani!

Kutshanje, i-Nanjing LimingBio's Novel Coronavirus (SARS-CoV-2) i-antigen yokufumanisa i-reagent "StrongStep® SARS-CoV-2 Antigen Rapid Test" ifumene ukuqinisekiswa kokusebenza kwe-Paul-Ehrlich-Institut (PEI*) eJamani, le mveliso iye yafunyanwa. iqinisekiswe yi-Arhente yaseJamani ye-Federal for Medicines and Medical Device Administration (BfArM).ILimingBio iye yaba ngomnye wabavelisi abambalwa eTshayina abafumene isatifikethi esiphindwe kabini se-BfArM+PEI eJamani.Uvavanyo olukhawulezayo lwe-antigen ye-Liming Bio luphumelele isiqinisekiso esigunyazisiweyo soMphathiswa wezeMpilo wamazwe amaninzi, engqina ngokupheleleyo ukusebenza kakuhle kwekhithi.
BONA OKUNGAKUMBI
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

IStrongStep® SARS-CoV-2 Antigen Rapid Test luvavanyo olukhawulezayo lwe-immunochromatographic ekubhaqweni kwe-antigen ye-COVID-19 ukuya kwintsholongwane ye-SARS-CoV-2 kwi-hum Throat/Nasopharyngeal swab.
BONA OKUNGAKUMBI
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.

Inoveli yeCoronavirus (SARS-CoV-2) Multiplex yeXesha lokwenyani PCR Kit

Le khithi yePCR enovakalelo kakhulu, elungele ukusetyenziswa iyafumaneka kwifomati ye-lyophilized (inkqubo yokumisa umkhenkce) yokugcina ixesha elide.Ikiti inokuthuthwa kwaye igcinwe kwiqondo lokushisa kwaye izinzile unyaka omnye.
BONA OKUNGAKUMBI

IIMVELISO ZETHU Zmva nje

KANINZI
about us

NGATHI

I-Nanjing Liming Bio-products Co., Ltd. yasekwa ngo-2001, inkampani yethu ikhethekileyo ekuphuhliseni, ekuveliseni nasekuthengiseni iimvavanyo ezikhawulezayo zezifo ezosulelayo ingakumbi ii-STD.Ngaphandle kwe-ISO13485, phantse zonke iimveliso zethu ziphawulwe nge-CE kwaye ivunyiwe yi-CFDA.Iimveliso zethu zibonise ukusebenza okufanayo xa kuthelekiswa nezinye iindlela (kubandakanya i-PCR okanye inkcubeko) edla ixesha kwaye ibiza.Ukusebenzisa iimvavanyo zethu ezikhawulezayo, nokuba ngabaguli okanye abaqeqeshi bezempilo banokonga ixesha elininzi lokulinda kuba ifuna nje imizuzu eli-10.

KANINZI
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