• 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!

Ua komo kā mākou huahana i ka papa inoa UK o nā mea hana diagnostic invitro i hoʻokuʻu ʻia!

Hiki iā ʻoe ke nānā i ka papa inoa ma ka pūnaewele UK Department of Health : https://www.gov.uk/.../medical-devices-regulations-2002... Inā pono ʻoe e kūʻai i kā mākou huahana, hiki iā ʻoe ke kelepona mai iā mākou ma i kēlā me kēia manawa!
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.

Hōʻike hōʻike hoʻāʻo a ma ka ʻike Silico no StrongStep® SARS-CoV-2 Antigen Rapid Test ma nā ʻano like ʻole SARS-CoV-2.

Ua hoʻololi ʻo SARS-CoV-2 i kekahi mau mutation me nā hopena koʻikoʻi, ʻo kekahi e like me B.1.1.7,B.1.351,B.1.2,B.1.1.28,B.1.617,Me ka omicron mutant strain(B1.1.529) hōʻike ʻia i nā lā i hala iho nei.Ma ke ʻano he mea hana IVD reagent, hoʻolohe mau mākou i ka hoʻomohala ʻana i nā hanana kūpono, e nānā i nā loli o nā waikawa amino kūpono a loiloi i ka hopena hiki ke hoʻololi i nā 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%.

ʻO StrongStep® SARS-CoV-2 Antigen Rapid Test E komo i ka papa inoa maʻamau o EU o ka maʻemaʻe a me ka palekana meaʻai.

ʻO StrongStep® SARS-CoV-2 Antigen Rapid Test E komo i ka papa inoa maʻamau o EU o ka hoʻomaʻemaʻe a me ka palekana o ka meaʻai, ʻo ia kekahi o nā mea hana liʻiliʻi i loaʻa ka 100% sensitivity ke emi ka waiwai o CT ma mua o 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.

ʻO StrongStep® SARS-CoV-2 Antigen Rapid Test i hoʻokomo ʻia i ka papa loiloi FIND

Hoʻokomo ʻia ka StrongStep® SARS-CoV-2 Antigen Rapid Test i ka papa inoa loiloi FIND.ʻO ka Foundation for Innovative New Diagnostics (FIND), he hui kūikawā i ka loiloi ʻana i ka hana o nā kits i ka launa pū ʻana me 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.

ʻO ka ʻōlelo e pili ana i nā virus like ʻole

Ua hōʻike ʻia ka nānā ʻana i ka hoʻohālikelike ʻana i ka pae mutation o ka ʻano SARS-CoV-2 i ʻike ʻia ma United Kingdom, South Africa a me India ʻaʻole i loko o ka ʻāpana hoʻolālā o ka primer a me ka probe i kēia manawa.ʻO StrongStep® Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit (ʻike no ʻekolu mau genes) hiki ke uhi a ʻike i nā ʻano mutant (i hōʻike ʻia ma ka papa aʻe) me ka ʻole o ka pili ʻana i ka hana i kēia manawa.No ka mea, ʻaʻohe hoʻololi i ka ʻāpana o ke kaʻina ʻike.
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.

Hōʻuluʻulu manaʻo o ka hōʻike loiloi mai ke kula ʻokoʻa ma 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

I kēia mau lā, ua loaʻa maikaʻi ka StrongStep® SARS-CoV-2 Antigen Rapid Test i hana ʻia e Nanjing Liming Bio-products Co. Ltd i ka palapala hōʻoia FDA Thailand (helu helu T 6400429,T 6400430,T 6400431,T 6400432), a ua loaʻa i kēia manawa. ʻae ʻia e komo i ka mākeke Thailand.
Recently, Nanjing LimingBio‘s Novel Coronavirus (SARS-CoV-2) antigen detection reagent

Ua loaʻa iā StrongStep® SARS-CoV-2 Antigen Rapid Test ka hōʻoia hana o Paul-Ehrlich-Institut (PEI) ma Kelemānia!

I kēia mau lā, ua loaʻa iā Nanjing LimingBio's Novel Coronavirus (SARS-CoV-2) antigen detection reagent "StrongStep® SARS-CoV-2 Antigen Rapid Test" i ka hōʻoia hana o Paul-Ehrlich-Institut (PEI*) ma Kelemānia, ua loaʻa kēia huahana. i hōʻoia ʻia e ka German Federal Agency for Medicines and Medical Device Administration (BfArM).Ua lilo ʻo LimingBio i kekahi o nā mea hana liʻiliʻi ma Kina i loaʻa ka palapala hōʻoia ʻelua o BfArM+PEI ma Kelemānia.Ua hala ka ho'āʻo wikiwiki antigen a Liming Bio i ka hōʻoia mana o ka Ministry of Health o nā ʻāina he nui, kahi e hōʻoiaʻiʻo pono ai i ka hana maikaʻi o ka pahu.
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.

ʻO SARS-CoV-2 Antigen Rapid Test

ʻO StrongStep® SARS-CoV-2 Antigen Rapid Test kahi hōʻike immunochromatographic wikiwiki no ka ʻike ʻana i ka antigen COVID-19 i ka maʻi SARS-CoV-2 i loko o ke kanaka Throat/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.

ʻO ka Novel Coronavirus (SARS-CoV-2) Pākuʻi PCR Manawa maoli

Loaʻa kēia pahu PCR maʻalahi a mākaukau e hoʻohana i ka format lyophilized (ka hana maloʻo maloʻo) no ka mālama lōʻihi.Hiki ke lawe ʻia a mālama ʻia ka pahu ma ka lumi wela a paʻa no hoʻokahi makahiki.

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ʻO Nanjing Liming Bio-products Co., Ltd. i hoʻokumu ʻia i ka makahiki 2001, ua loea kā mākou hui i ka hoʻomohala ʻana, ka hana ʻana a me ke kūʻai aku ʻana i nā hoʻokolohua wikiwiki no nā maʻi maʻi maʻi ma kahi o nā STD.Ma waho aʻe o ISO13485, kokoke i kā mākou huahana āpau i hōʻailona ʻia ʻo CE a ʻae ʻia ʻo CFDA.Ua hōʻike ʻia kā mākou huahana i nā hana like i hoʻohālikelike ʻia me nā ʻano hana ʻē aʻe (me ka PCR a i ʻole ka moʻomeheu) e hoʻopau i ka manawa a me ke kumu kūʻai.Ke hoʻohana nei i kā mākou hoʻāʻo wikiwiki, hiki i nā mea maʻi a i ʻole nā ​​limahana mālama ola ke mālama i ka manawa he nui no ke kali ʻana no ka mea he 10 mau minuke wale nō.

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