IsiShayina
English
  • 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!

Imikhiqizo yethu ingene ohlwini lwase-UK lwemishini yokuxilonga i-coronavirus invitro ekhululiwe!

Ungabheka uhlu kusizindalwazi soMnyango Wezempilo wase-UK : https://www.gov.uk/.../medical-devices-regulations-2002... Uma udinga ukuthenga imikhiqizo yethu, ungasithinta ku- noma nini!
BUKA OKWENGEZIWE
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.

Umbiko Wokuhlola kanye Nokuhlaziywa Kwe-Silico kwe-StrongStep® SARS-CoV-2 Antigen Rapid Test ku-Different SARS-CoV-2 Variant

I-SARS-CoV-2 manje isiguqule izakhi zofuzo ezimbalwa ezinemiphumela emibi kakhulu, eminye efana 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) kubikwe ezinsukwini zakamuva.Njengomkhiqizi we-IVD reagent, sihlala sinaka ukuthuthukiswa kwemicimbi efanele, sihlola izinguquko zama-amino acid afanelekile futhi sihlole umthelela ongaba khona wokuguqulwa kwezakhi zofuzo kuma-reagents.
BUKA OKWENGEZIWE
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 Faka uhlu olujwayelekile lwe-EU lwenhlanzeko nokuphepha kokudla

I-StrongStep® SARS-CoV-2 Antigen Rapid Test Faka uhlu olujwayelekile lwe-EU lwenhlanzeko nokuphepha kokudla, okungenye yabakhiqizi abambalwa abanokuzwela okungu-100% lapho inani le-CT lingaphansi kwama-25%.
BUKA OKWENGEZIWE
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.

I-StrongStep® SARS-CoV-2 Antigen Rapid Test ifakwe ohlwini lokuhlola lwe-THOLA

I-StrongStep® SARS-CoV-2 Antigen Rapid Test ifakwe ohlwini lokuhlola lwe-THOLA.I-Foundation for Innovative New Diagnostics (FIND), yinhlangano egxile ekuhloleni ukusebenza kwekhithi ngokubambisana kwamasu ne-WHO.
BUKA OKWENGEZIWE
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.

Isitatimende samagciwane ahlukile

Ukuhlaziywa kokulandelana kokuqondanisa kubonise ukuthi isiza soguquko sokuhluka kwe-SARS-CoV-2 esibonwa e-United Kingdom, eNingizimu Afrika nase-India zonke azikho endaweni yokuklama ye-primer kanye nophenyo okwamanje.I-StrongStep® Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit (itholwa izakhi zofuzo ezintathu) ingamboza futhi ibone izinhlobo eziguqukayo (eziboniswe kuthebula elilandelayo) ngaphandle kokuphazamisa ukusebenza kwamanje.Ngoba alukho ushintsho endaweni yokulandelana kokutholwa.
BUKA OKWENGEZIWE
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.

Fingqa Umbiko Wokuhlola Ovela Ku-Different Institute on 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.
BUKA OKWENGEZIWE
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.

I-Thailand FDA COVID 19 ATK 2021 T6400429

Muva nje, i-StrongStep® SARS-CoV-2 Antigen Rapid Test ekhiqizwa yi-Nanjing Liming Bio-products Co. Ltd ithole ngempumelelo isitifiketi se-Thailand FDA (inombolo yokubhalisa T 6400429, T 6400430, T 6400431,T 6400432 ), futhi manje isitholakele. kugunyazwe ukungena emakethe yaseThailand.
BUKA OKWENGEZIWE
Recently, Nanjing LimingBio‘s Novel Coronavirus (SARS-CoV-2) antigen detection reagent

I-StrongStep® SARS-CoV-2 Antigen Rapid Test ithole ukuqinisekiswa kokusebenza kwe-Paul-Ehrlich-Institut (PEI) eJalimane!

Muva nje, i-Nanjing LimingBio's Novel Coronavirus (SARS-CoV-2) i-antigen regent ye-"StrongStep® SARS-CoV-2 Antigen Rapid Test" ithole ukuqinisekiswa kokusebenza kwe-Paul-Ehrlich-Institut (PEI*) eJalimane, lo mkhiqizo uqinisekisiwe. kuqinisekiswe i-German Federal Agency for Medicines and Medical Device Administration (BfArM).I-LimingBio isibe ngomunye wabakhiqizi abambalwa e-China abathole isitifiketi esikabili se-BfArM+PEI eJalimane.Ukuhlolwa okusheshayo kwe-antigen ye-Liming Bio kuphumelele isitifiketi esigunyaziwe soMnyango Wezempilo wamazwe amaningi, okufakazela ngokugcwele ukusebenza okuhle kakhulu kwekhithi.
BUKA OKWENGEZIWE
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.

Ukuhlolwa Okusheshayo kwe-SARS-CoV-2 Antigen

I-StrongStep® SARS-CoV-2 Antigen Rapid Test iyisivivinyo esisheshayo se-immunochromatographic ukuze kutholwe i-COVID-19 antigen kugciwane le-SARS-CoV-2 ku-human Throat/Nasopharyngeal swab.
BUKA OKWENGEZIWE
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.

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

Le kit ye-PCR ezwela kakhulu, elungele ukusetshenziswa itholakala ngefomethi ye-lyophilized (inqubo yokumisa iqhwa) ukuze igcinwe isikhathi eside.Ikhithi ingathuthwa futhi igcinwe ekamelweni lokushisa futhi izinzile unyaka owodwa.
BUKA OKWENGEZIWE

IMIKHIQIZO YETHU YAkamuva

OKUNINGI
about us

MAYELANA NATHI

I-Nanjing Liming Bio-products Co., Ltd. eyasungulwa ngo-2001, inkampani yethu ibikhethekile ekuthuthukiseni, ekukhiqizeni nasekukhangiseni izivivinyo ezisheshayo zezifo ezithathelwanayo ikakhulukazi izifo ezithathelwana ngocansi.Ngaphandle kwe-ISO13485, cishe yonke imikhiqizo yethu imakwe nge-CE futhi igunyaziwe yi-CFDA.Imikhiqizo yethu ibonise ukusebenza okufanayo uma kuqhathaniswa nezinye izindlela (okuhlanganisa i-PCR noma isiko) ezidla isikhathi futhi ezibizayo.Ngokusebenzisa izivivinyo zethu ezisheshayo, isiguli noma ochwepheshe bezokunakekelwa kwempilo bangonga isikhathi esiningi sokulinda ngoba kudinga nje imizuzu eyi-10.

OKUNINGI
BHALISA
  • Facebook
  • Linkedin
  • Tittwer
  • youtube
  • Instagram
  • Pinterest
Amalungelo ©2016-2021 : Wonke Amalungelo Agodliwe.南京黎明生物制品有限公司 苏ICP备09058001号-2 Imikhiqizo Eshisayo - Imephu yesayithi
Ukuhlolwa kwe-Human Coronavirus Igm/Igg Antibody, Ikhithi Yokuhlola I-Antibody, ICoronavirus Yokuhlola I-Covid-19, I-Novel Coronavirus 2019 Ncov, Ukuhlolwa kwe-Cryptococcal Antigen, I-Covid-19 Rapid Test Kit,
Chofoza u-enter ukuze useshe noma u-ESC ukuze uvale