The Precision Hand Held Reader Drug Test Cassette is a fast visual, competitive panel immunoassay that can be used for the qualitative detection of drug metabolites at specific cutoff levels in human Saliva Up to 99% Accurate Immediate Results Shelf-life up to 18 months Collect the specimen with collector Read the results immediately Ideal for low-volume donations These drug tests are intended for workplace testing & forensic use ONLY (not FDA cleared or CLIA waived).
The Discover Drug Test Cassette is a fast visual, competitive panel immunoassay that can be used for the qualitative detection of drug metabolites at specific cutoff levels in human Saliva Up to 99% Accurate Immediate Results Shelf-life up to 18 months Collect the specimen with collector Add 3 drops to the well Read the results immediately Ideal for low-volume donations These drug tests are intended for workplace testing & forensic use ONLY (not FDA cleared or CLIA waived).
The CareStart COVID-19 Antigen test kit allows for the rapid screening of COVID-19 infection on a large scale, with results in just 10 minutes. The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from individuals who are suspected of COVID-19 by their healthcare providers. This product is CLIA waived under FDA/EUA authorization. Quantity: 8 Million test kits MOQ: 1 Million FOB: New Jersey USA Price: 11.75 USD
Covid-19 Antibody IgM/IgG Rapid Test kit, Using whole blood, Serum, Plasma sample, take less than 10 minutes, a lateral flow immunochromatographic assay for detaction of SAR-CoV-2 IgM/IgG antibodies in human blood specimens. Package Unit: 25 tests/kit 25 test devices 1 Assay buffer 25 blood transfer pipettes
Certification - Test report/CE/FDA Daily manufacturer output - 10,000,000 Pcs Price - $3.00 Quantity Derived
Certification - Test Report/CE Daily manufacturer output - TBD Price - $25 Volume dependent
Certification - Test report/CE/FDA Daily manufacturer output - 10,000,000 pcs Price - $3.00 Quantity Derived
COVID-19 IgG/IgM Rapid Antibody Test Kit with EUA FDA approval. Available immediately! (Whole Blood/Serum/Plasma) is a solid phase immuno chromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to 2019 Novel Coronavirus in human whole blood, serum or plasma. - Fast results as soon as 2-10 minutes - Facilitates patient treatment decisions quickly - Simple, time-saving procedure - Little specimens, only 5L of serum/plasma or 10L of whole blood specimens - All necessary reagents provided & no equipment needed - High sensitivity and specificity - Sensitivity: IgG 97.2%; IgM 87.9% - Specificity: IgG 100%; IgM 100% - Specimen: Whole Blood, Serum, Plasma - Shelf Life: 24 months from the date of manufacture
The Coronavirus Ag Rapid Test Cassette (Swab) is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP) swab specimens directly or after the swabs have been added to viral transport media from individuals who are suspected of COVID-19 by their healthcare provider. It is intended to aid in the rapid diagnosis of SARS-CoV-2 infections. The Coronavirus Ag Rapid Test Cassette (Swab) does not differentiate between SARS-CoV and SARS-CoV-2.
GeneFinder COVID-19 Plus RealAmp kit is the One-Step Reverse Transcription Real-Time PCR Kit designed to detect Novel Corona Virus (COVID-19) qualitatively through Reverse Transcription reaction and Real-Time Polymerase Chain Reaction Main Features: -Target Genes: RdRp, N and E gene -120 minutes detection for COVID-19 -Reverse Transcription reaction and Real-Time Polymerase Chain Reaction -Easy-to-use (One-Tube) and interpretation -Reliable Result by internal/ Positive/ Negative control Contact us for more info.
M nCov Real-Time Detection Kit is used for identificatino and detection of novel coronavirus (2019-nCoV) ORF1ab (RdRp) gene and E gene in human nasopharyngeal swab, oropharyngeal swab, and sputum specimens using reverse transcription (RT) Real-time PCR. This kit is helpful for the auxiliary diagnosis of 2019 novel coronavirus disease (COVID-19). The test results are for clinical reference only and cannot be used as basis for confirming or excluding cases alone. Advantages of Stadndard M nCoV - Designed according to WHO/ KCDC recommendations -Easy to use 1 Tube reaction -Separately configured Internal Control (IC) to verify the whole process -Simple interpretation of results (2 Target (RdRp/ E gene) + 1IC -Outstanding analytical sensitivity 5 copies/ reaction -A wide range of instrument compatibility CFX96 / AB7500/ LC480 -Fast TAT - within 90 minutes after extraction -12 months of stability -CE-IVD, KEUA (Korean Emergency Use Authorization)
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Rapid Malaria pv./pf Test Kit The One Step Malaria (P.f./P.v.) Test is a rapid chromatographic immunoassay for the qualitative detection of plasmodium falciparum Histidine Rich Protein-II (HRP-II) and plasmodium vivax Lactate Dehydrogenase (LDH) in Whole Blood to aid in the diagnosis of Malaria (P.f./P.v.).
On May 27th, 2022, Boson Rapid SARS-CoV-2 Antigen Test Card (Self-Testing) was authorized for marketing by Health Canada.Global Technology Foundation is a fully authorized independent distributor of Boson Biotechnology Co., Ltd. throughout North America. It has the ability to supply government and private buyers with a monthly supply of 30-40 million boxes. The quotation on this page is only for the USA .Sales, OTG supply, accept TT payment.The BOSONTM� Rapid SARS-CoV-2 Antigen Test Card (Home Test) has been sold to Europe, Southeast Asia, Australia, Canada and other countries, with excellent product quality and service. The test gained substantial popularity among users. The only supplier with the lowest price in North America for COVID-19 antigen test kits
The US Food and Drug Administration (FDA) granted Emergency Use Authorization for the BOSONTM Rapid SARS-CoV-2 Antigen Test Card (Home Test) on April 6, 2022. Global Technology Foundation is a fully authorized independent distributor of Boson Biotechnology Co., Ltd. throughout North America. It has the ability to supply government and private buyers with a monthly supply of 30-40 million boxes. The quotation on this page is only for the USA .Sales, DDP supply, accept TT payment.The BOSONTM� Rapid SARS-CoV-2 Antigen Test Card (Home Test) has been sold to Europe, Southeast Asia, Australia, Canada and other countries, with excellent product quality and service.  The test gained substantial popularity among users
SOP #1) ICPO, POF- Then fully financed, we move the product here and buyer must pay within 24hrs after it arrives CIF (Inspect and Pay) $7.89 - add comms CIF USA : Within 6 working days all packages will be arrived by air freight or #2) PAYMENT TERM PO , 50% after PO / 50% after BOL is provided. CIF USA : Within 6 working days all packages will be arrived by air freight $6.89 - add comms PO: Ruben L Hudson Advanced Healthcare Resources LLC c/o STM Bio - Goldmanifestor
CE Approved MAU is a rapid visual immune-assay for the qualitative, presumptive detection of albumin in urine for self-testing. The test used as a supplementary method in the diagnosis of diabetic nephropathy and other renal damage. MAU occurs when the kidney leaks small amounts of albumin into the urine. The first indicator of a renal dysfunction, especially for diabetic patients Independent risk indicator to evaluate the profession of chronic kidney disease (CKD).
Bacterial Vaginosis Quick Test Kit is designed as a simple, rapid, cost effective method for in vitro testing. It is qualitative test for the determination of neuraminidase (SNa) in female vaginal fluid, which is auxiliary diagnosis of bacterial vaginosis. Application Used to assist the diagnostic of bacterial vaginosis, evaluate the micro ecological balance in genital tract, and to prevent recurrences of vaginosis. Advantage High sensitivity, strong specificity Easy operation, convenient and effective No need of special instrument, no need of professional training
CE Approved The Follicle Stimulating Hormone (FSH) Test Kit is a rapid qualitative test for detect FSH in urine. This help to check the function of the pituitary gland and check if hormone levels are normal. The test can be used to see if a woman has started the menopause. The test may also be used (along with other tests) for detecting possible causes of both male and female infertility. Self-detection of ovarian function Guide to prevention of premature ovarian Diagnosis of menopause