$1.00 for 10,000-499,000 pcs $0.98 from 500,000 pcs Commission: $0.00 mark up: allowed - 50% Seller/50% buyer Delivery: ExWork Hangzhou, China Payment: 100% TT before loading â?? 1 box = 500 pcs 1 box = 18,30 kg
$1.08 for 10,000-499,000 pcs $1.06 from 500,000 pcs Commission: $0.00 mark up: allowed - 50% Seller/50% buyer Delivery: ExWork Zhejiang, China Payment: 100% TT before loading 1 box = 480 pcs 1 box = 11,50 kg
$1.15 for 10,000-99,000 pcs $1.13 for 100,000-499,000 pcs $1.11 for 500,000-1,000,000 pcs Commission: $0.00 mark up: allowed - 50% Seller/50% buyer Delivery: ExWork Beijing, China Payment: 100% TT before loading 1 box = 320 pcs 1 box = 10,37 kg
The PocRoc SARS-CoV-2 Antigen Rapid Test Kit (TRFIA) is an immunofluorescent sandwich assay. It can detect the virus with very high sensitivity and specificity. When the sample is applied to the sample wells, SARS-CoV N protein and labeled antibody complexes are formed and travel up the strip. The labeled microsphere fluorescent probe reagent is used to form a visible red line with a matched UV flashlight. The presence of SARS-CoV-2 will be indicated by a visible red test line (T) in the result window. The membrane is pre-coated with Chicken IgY on the control (C) line. Control (C) line appears in each result window when the sample has flowed through the strip.
The PocRoc SARS-CoV-2 Antigen Rapid Test Kit(Colloidal Gold)is used for qualitative detection of SARS-CoV-2 virus nucleocapsid protein, which is an important conserved structural protein of SARS-CoV-2 in human nasal/ oropharyngeal samples. The detection of SARS-CoV-2 nucleocapsid protein antigen can be used to assist the diagnosis of novel coronavirus infection and is helpful for the early detection of novel coronavirus pneumonia infection in the latent period.
HCG Test is an immunochromatographic assay designed for qualitative determinatrion of human chronic gonadotropin (hCG) in urine for the detection of pregnancy. Human chorionic gonadotropin is a glycopeptide hormone produced by the placenta during pregnancy. The apprearance and rapid rise in the concentration of hCG in the woman''s urine makes it good pregnancy marker. Usually, concentration of hCG in urine is at least 25mlU/ml within seven to ten days after conception. Justifying our reputation in this market, we are readily immersed in the arena of offering to our patrons a broad consignment of HCG Tests Kits. Sensitivity 25 miu Features: Precise design Durable Good quality
Nasal and antibody covid 19 test kit
Covid Test Kit -19 FDA approved
FDA Approved Covid anti body test kit
Covid test kit, FDA approved
Covid test kit
Multi-drug One Step 2-15 Urine Drug Test Cup (MOP, MET, KET, AMP, BAR, BUP, BZO, COC, COT, MDMA, THC, MTD, OPI, PCP, TCA)
A rapid, one step test for the qualitative detection of Amphetamines in human urine. For healthcare professionals including professionals at point of care sites For professional in vitro diagnostic use only. A drug-free urine pool was spiked with Amphetamine at the following concentrations: 0 ng/mL, 500 ng/mL, 750 ng/mL, 1,000 ng/mL, 1,250 ng/mL and 1,500 ng/mL. The result demonstrates >99% accuracy at 50% above and 50% below the cut-off concentration. The data are summarized below: AMP Concentration (ng/mL)Percent of CutoffnVisual Result NegativePositive 00%30300 500-50%30300 750-25%30237 1,000Cutoff30921 1,250+25%30129 1,500+50%30030
Disposable face masks, covid antigen tests, pulse oximeter.
Sensitivity: 95.06% Specificity: 99.62% Content of each kit: Test card (innovative and unique system), detailed instructions for use, sterile disposable swab, reactive solution for sample treatment, illustrative manual for use and operation. General characteristics: CE self-diagnostic certification, holographic security label with individual code for authenticity verification, non-invasive, easy to use, no prescription required, rapid results in less than 15 minutes, high precision. Sale restrictions: Exclusive sale to pharmacies, authorized companies, pharmaceutical distribution, socio-sanitary establishments, health establishments, occupational risk prevention, public organizations and health professionals. Restricted sale to individuals. Sale subject to the provisions of Royal Decree 588/2021, of July 20, which modifies Royal Decree 1662/2000, of September 29, on medical devices for "in vitro" diagnosis, in order to regulate the sale to the public and the advertising of covid-19 self-diagnosis products. Sale subject in relation to tax matters to the provisions of Royal Legislative Decree 35/2020, of December 22, seventh final provision. Applicable tax rate of Value Added Tax to deliveries, imports and intra-community acquisitions of certain goods and provision of services necessary to combat the effects of SARS-CoV-2 as well as for the purposes of the special regime of the equivalence surcharge .
The Treponema pallidum Antibody Assay Kit (Colloidal Gold) is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) to Treponema pallidum (Tp) in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with Tp.
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The test is a rapid colloidal gold immunochromatographic assay for the in vitro qualitative detection of the novel coronavirus(SARS-CoV-2), the influenza A virus (FluA) and the influenza B(FluB) antigen in human nasopharyngeal swab, oropharyngeal swab, nasal swab, and saliva samples from individuals suspected of respiratory viral infection.
The kit is intended for the in vitro qualitative determination of Novel Coronavirus (2019-nCoV) IgG/IgM antibody in human serum, plasma or whole blood. Testing is limited to supplementary detection indicator for suspected nucleic acid negative results or in conjunction with nucleic acid detection in the diagnosis of suspected cases. It should not be used as the basis for diagnosis and exclusion of Novel Coronavirus Pneumonia.
The kit is used to qualitatively detect the novel coronavirus (SARS-CoV-2) nucleocapsid protein antigen in human nasal swab samples in vitro. In the acute phase of infection, antigens are usually detectable in upper respiratory tract specimens.
