• 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!

Alaabtayadu waxay galeen liiska UK ee aaladaha ogaanshaha invitro ee coronavirus-ka laga dhaafay!

Waxaad ka hubin kartaa liiska bogga internetka ee Waaxda Caafimaadka UK: https://www.gov.uk/.../medical-devices-regulations-2002... Haddii aad u baahan tahay inaad iibsato alaabtayada, waxaad nagala soo xidhiidhi kartaa at wakhti kasta!
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.

Warbixinta Tijaabada iyo Falanqaynta Silico ee StrongStep® SARS-CoV-2 Tijaabada Degdegga ah ee Antigen ee Kala duwanaanta SARS-CoV-2

SARS-CoV-2 waxay hadda horumarisay dhowr isbedel oo leh cawaaqib xun, qaar sida B.1.1.7, B.1.351, B.1.2, B.1.1.28, B.1.617, oo ay ku jiraan omicron mutant strain (B1.1.529) ayaa la sheegay maalmihii la soo dhaafay.Sida soo saaraha reagent IVD, waxaan had iyo jeer fiiro gaar ah u leh horumarinta dhacdooyinka khuseeya, hubi isbeddelada asiidhyada amino ee khuseeya iyo qiimaynta saamaynta suurtagalka ah ee isbeddellada on 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 Tijaabada Degdegga ah ee Antigen-ka Geli liiska guud ee EU ee nadaafadda iyo badbaadada cuntada

StrongStep® SARS-CoV-2 Tijaabada Degdegga ah ee Antigen Geli liiska guud ee EU-da ee nadaafadda iyo badbaadada cuntada, taas oo ah mid ka mid ah dhowr warshadood oo leh 100% dareenka marka qiimaha CT uu ka yar yahay 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 Tijaabada Degdegga ah ee Antigen-ka ee lagu daray liiska qiimeynta ee HEL

StrongStep® SARS-CoV-2 Tijaabada Degdegga ah ee Antigen-ka ayaa lagu daray liiska qiimeynta FIND.Aasaaska cusub ee ogaanshaha cusub (FIND), waa urur ku takhasusay qiimeynta waxqabadka xirmooyinka ee iskaashiga istiraatiijiyadeed ee 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.

Warbixin ku saabsan fayraska kala duwan

Falanqaynta isku xigxiga ee falanqaynta ayaa muujisay in goobta isbeddelka ee kala duwanaanshaha SARS-CoV-2 ee lagu arkay Boqortooyada Ingiriiska, Koonfur Afrika iyo Hindiya aysan dhammaantood ku jirin gobolka naqshadeynta ee asaasiga ah iyo baaritaanka hadda.StrongStep® Novel Coronavirus (SARS-CoV-2) Qalabka PCR ee-waqtiga-dhabta-dhabta ah (ogaanshaha saddexda hidde-side) ayaa dabooli kara oo ogaan kara noocyada mutant (oo lagu muujiyey shaxda soo socota) iyada oo aan wax saameyn ah ku yeelan waxqabadka hadda.Sababtoo ah ma jiro wax isbeddel ah oo ku yimid gobolka ee isku xigxiga ogaanshaha.
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.

Soo koobida Warbixinta Qiimaynta ee Machadka Kala duwan ee 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

Dhawaan, StrongStep® SARS-CoV-2 Antigen Rapid Test oo ay soo saartay Nanjing Liming Bio-products Co. Ltd ayaa si guul leh u heshay shahaadada FDA ee Thailand (lambarka diiwaangelinta T 6400429,T 6400430,T 6400431,T 6400432) loo ogolaaday inuu galo suuqa Thailand.
Recently, Nanjing LimingBio‘s Novel Coronavirus (SARS-CoV-2) antigen detection reagent

StrongStep® SARS-CoV-2 Antigen Rapid Test ayaa helay xaqiijinta waxqabadka Paul-Ehrlich-Institut (PEI) ee Jarmalka!

Dhawaan, Nanjing LimingBio's Novel Coronavirus (SARS-CoV-2) reagent ogaanshaha antigen "StrongStep® SARS-CoV-2 Antigen Rapid Test" wuxuu helay xaqiijinta waxqabadka Paul-Ehrlich-Institut (PEI *) gudaha Jarmalka, badeecadan ayaa ahayd shahaado ay siisay Wakaaladda Federaalka Jarmalka ee Dawooyinka iyo Maamulka Qalabka Caafimaadka (BfArM).LimingBio waxay noqotay mid ka mid ah soosaarayaasha yar ee Shiinaha ee helay shahaadada labadaba ee BfArM+PEI ee Jarmalka.Tijaabada degdega ah ee antigen-ka ee Liming Bio ayaa ka gudubtay shahaadada awooda leh ee Wasaaradda Caafimaadka ee wadamo badan, taas oo si buuxda u caddaynaysa waxqabadka wanaagsan ee xirmada.
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.

Baaritaanka degdega ah ee antigen-ka SARS-CoV-2

StrongStep® SARS-CoV-2 Antigen Rapid Test waa baaritaan degdeg ah oo immunochromatographic ah oo lagu ogaanayo COVID-19 antigen ilaa fayraska SARS-CoV-2 ee ku jira dhuunta bini'aadamka / naasopharyngeal.
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) Qalabka PCR-waqtiga-dhabta ah ee Multiplex

Xirmadan aadka u xasaasiga ah, ee diyaar u ah in la isticmaalo PCR waxa lagu heli karaa qaab lyophilized ah (habka qalajinta qaboojinta) kaydinta muddada dheer.Qalabka waxa lagu rari karaa oo lagu kaydin karaa heerkulka qolka waana mid deggan muddo hal sano ah.

Agabkeenii ugu dambeeyay

NAGU SAABSAN

Nanjing Liming Bio-products Co., Ltd. oo la aasaasay 2001, shirkadeena waxay ku takhasustay horumarinta, soo saarista iyo suuqgeynta tijaabooyinka degdega ah ee cudurada faafa gaar ahaan STDs.Marka laga reebo ISO13485, ku dhawaad ​​​​dhammaan badeecadaheena waa calaamad CE iyo CFDA waa la ansixiyay.Badeecadahayadu waxay muujiyeen waxqabad la mid ah marka loo eego hababka kale (oo ay ku jiraan PCR ama dhaqanka) kuwaas oo waqti badan qaata oo qaali ah.Isticmaalka imtixaanadayada degdega ah, ama bukaan-socodka ama xirfadlayaasha daryeelka caafimaadku waxay badbaadin karaan waqti badan sugitaan sababtoo ah waxay u baahan tahay 10 daqiiqo oo keliya.

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