Diagnostic Kits Suppliers and Manufacturers

OFFER DATE: 2022/02/06 HOME TESTING KIT FLOWFLEX & iHealth & Celltrion and others OTG & DDP USA We can supply them with the best offer of the above testing kits Waiting for your reply, Jay

We are the authorized distributing partner of the South Korean diagnostic manufacturer BioTNS. Our role is to distribute in South Korea and overseas the Covid-19 RT-PCR PNA kits. 1 kit allows you to test 100 patients. - CE approved - US FDA approved Contact us to receive your quotation.

DiaPlexQ Novel Coronavirus (2019-nCoV) Detection Kit Real-Time OneStep RT-PCR based assay system for detection of SARS-CoV-2 [Product Approval] U.S FDA EUA, Health Canada IO, CE-IVD marked The DiaPlexQ Novel Coronavirus (2019-nCoV) Detection Kit is a real-time reverse transcriptase (RT)-PCR test intended for the qualitative detection of nucleic acid from SARS-CoV-2 in nasopharyngeal swabs, oropharyngeal (throat) swabs, anterior nasal swabs, mid-turbinate nasal swabs, nasal aspirates, nasal washes, bronchoalveolar lavage (BAL) fluid and sputum from individuals suspected of COVID-19 by their healthcare provider. Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. The agent detected may not be the definite cause of disease. Positive results do not rule out bacterial infection or co-infection with other viruses. Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information. The DiaPlexQ Novel Coronavirus (2019-nCoV) Detection Kit is intended for use by qualified clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures.

The CERA-PET Multi Test meter (M 400V) is intended for use in veterinary and medical professional setting to monitor blood glucose, lactate level in dogs and cats. It is also intended for use in the home setting to monitor blood glucose, lactate levels in dogs and cats. The CERA-PET Multi Test Meter is intended for in vitro diagnostic use.

The CERA-CHEK1Code Blood Glucose Monitoring System is intended to help people manage their diabetes with measuring their glucose level with fresh capillary whole blood the fingertip, the palm, the forearm, the upper arm, the thigh, or the calf for self-testing. It also provides professional healthcare personnel with the helpful information with measuring glucose concentration in fresh capillary whole blood. The CERA-CHEK 1Code Blood Glucose Monitoring System is intended for in vitro diagnostic use.

Handheld Glucose, Lipid(TC, TG, HDL, Cal-LDL) Monitoring System The GREENCARE LIPID is an in vitro diagnostic medical device for measurements of total cholesterol, triglycerides, HDL cholesterol in whole blood by colorimetric assay with enzyme reaction. And the GREENCARE LIPID is an in vitro diagnostic medical device that can diagnose diabetes by measuring blood glucose through electrochemical reactions.

DESCRIPTION * Detection of Sars-Cov-2 with reverse transcption Real time PCR ( TAT 2.0 hr ) * Amplify N gene and RdRp(orf1ab) gene of Sars-Cov2 AVAILABLE SAMPLE TYPE * Sputum * Oropharyngeal ( OP ) and nasopharyngeal ( NP ) swabs

This is rapid chromatographic immunoassay for the qualitative detection of Coronavirus(SARS- Co-V-2) IgM and lgG antibody in serum, plasme, whole blood specimens. Features & Benefits -Easy Procedure -No instruments needs -Specimen : Serum, plasmam, whole blood 10 -Reading Time: 10~15 min -Storage : 2~30

Pcr Test Kits / 1 Kit = 100tests / Made In Korea

COVID-19 Real Time RT-PCR Kit detects the novel corona virus, COVID-19 using one-step real-time RT-PCR in a single tube. The target genes for the detection of the virus are Orf1 ab and N gene. The kit includes primers and probe set targeting the human Rnase P gene that serves as an internal positive control for the real-time RT-PCR. Ordering Info : 96 Tests/Kit (MOQ : 10 Kits)

BioFACT Viral RNA/DNA Prep Kit is designed to isolate viral RNA/DNA from virous samples such as serum, plasma, cell-culture media, cell free body fluids and tissue. Highly purified viral RNA/DNA from Coronavirus(COVID-19), Adenovirus, Norovirus, Zikavirus, HCV, HIV and Yellow fiber virus can be isolated through the kit. -Isolation of pure viral RNA/DNA from virus samples -No carrier RNA required -Glass fiber membrane column based -Safety use : No phenol nor chloroform -Quantitative PCR (qPCR, qRT-PCR) -Pathogen detection -Poly-A detection -cDNA synthesis -Microarray -Northern blotting

COVID-19 Self Swab Test Kit is the first commercialized Black Gold Particle technology in the world (High Sensitivity & Specifity) -It's made as User friendly Dual Color System (Control Line: Red, Test Line: Black) -Rapid Test Time takes 5~8 Min. -It's intended to use for detection of SARS-CoV2 antigen -20 Tests / Kit (Box) -Tester indicates Negative(C: Red), Positive(C: Red & T: Black) and Invalid(No "C")

This kit is called CTM(Clinical Virus Transport Medium). CTM is intended for the collection and transport of clinical specimen containing Corona Virus and others. Collected Samples by each Nasopharyngeal Swab and Oropharyngeal Swab can be preserved in One Virus Transport Medium(CTM) simultaneously. -Nasopharyngeal Swab : Tilt the patient's head back slightly to straighten the passage from the front of the nose, and gently inset the swab along the base of the nose(not upwards) until it reaches the nasopharynx-gentle rotation of the swab for a few seconds may be helpful. -Oropharyngeal Swab : Press the tongue and extract the secretion from the back wall of pharynx.

1. Product Overview -EnSave is â??IMPROVER of COMBUSTION EFFICIENCY for INTERNAL COMBUSTION ENGINEâ?? operated by â??CATALYSTâ?? which is created from chemical reaction by rare earth element and precious metal such as platinum, lanthanum, &, etc. -EnSaveâ??s Catalytic Action acts to Enhance the Combustion Efficiency of the engine by leading close to perfect combustion. - As a result, EnSave realizes both â??FUEL SAVING and FUEMS SAVING - â??Double Effectâ?? at the same time, the Remarkable and Innovative Technology is under Patent Pending now. 2. Effectiveness 1) Improving Fuel Efficiency (5~20%): Save fuel cost & Profit-up 2) Engine Power up Higher Combustion Efficiency leads to Engine Power-up 3) Fumes Down: Makes Eco-friendly Green Car 4) Noise & Shaking Down: Driving Fatigue & Stress Down 5) Simple & Easy Installation: Just put EnSave into Air Cleaner Space, No A/S required

1. Sample: Blood (Whole blood, Serum) 2. Measuring Time: 10~15 Minutes 3. Test Principle - Identification of COVID 19 antibody in blood COVID 19 IgG / IgM Rapid Test (WB / Serum / Plasma in human blood) is a fast chromatographic immunoassay for qualitative analysis of IgG and IgM antibodies to COVID 19. 4. Characteristics - Simplicity: No special equipment required and intuitive visual interpretation. - Rapid: Fast sampling with blood at the tip of the finger, results in 10~15 minutes. 5. Main Use - People with symptoms - Suspicious with or without mil d symptoms patient. - It is also used to test people in close contact with infected patients and those in quarantine.

The COVID-19 RT-PCR Peptide Nucleic Acid (PNA) KIT is a real-time reverse transcription (RT)-Polymerase chain reaction (PCR) assay intended for the qualitative detection of nucleic acid from SARS-CoV-2 in respiratory specimens such as nasopharyngeal swabs, oropharyngeal swabs, anterior nasal swabs, midturbinate nasal swabs, bronchoalveolar lavage (BAL), and nasopharyngeal wash/aspirates or nasal aspirates collected from individuals suspected of COVID-19 by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests. Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in upper respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out a bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities. Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information. The COVID-19 RT-PCR PNA KIT is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures. The COVID-19 RT-PCR PNA KIT is only for use under the Food and Drug Administrations Emergency Use Authorization.

Unit Price: USD 15 Target Region: RdRP, E gene, N gene Accuracy: 100% Recommended PCR: CFX96 Real Time PCR System (Bio Rad) DTprime DT-96 QIAGEN Rotor-Gene Q Box Size: Size: W 80 x D 80 x H 65 (mm) Weight: 45g / box Certification: Korea GMP (ISO 13485 2003) European CE

Unit Price: USD 16 Target Region: RdRp, E gene Accuracy: 100% Recommended PCR: Roche Light Cycler 480 Qiagen Rotor-Gene Q plex HRM Applied Biosystems Quantstudio5 Applied Biosystems 7500 Real-Time PCR system Bio-RAD CFX96 Real-Time PCR Detection system Certification: ISO 13485 European CE Health Canada Saudi Arabia FDA

Unit Price: USD 10 Accuracy: 95% Box Size: L 22* W 13* D 7 cm Certificates EN ISO 13485:2016 Adopted Technical Standards IVD directive 98/79/EC, EN ISO13485:2016, EN ISO 14971:2012, EN ISO 18113 1:2011, EN 13975:2003 EN ISO 13612:2002, EN ISO 15223 1:2016, EN ISO 23640:2015 EN ISO 17511:2003