Place of Origin: China Brand Name: OEM Model Number: HHI-402 Power Source: manual Warranty: 2 years After-sale Service: Return and Replacement Material: Plastic Shelf Life: 2 years Quality Certification: CE Instrument classification: Class II Safety standard: None Type: Pathological Analysis Equipments Product name: One step blood self rapid kit HIV home test Application: Home base, online-shop Read time: 10-15 mins Specimen: Whole blood, plasma, serum Accuracy: 99% Format: Cassette Expiry date: 24 months Certification: ISO13485, ISO9001 OEM: Available
If anyone is looking for Genbody Self Test Kits and nitrile gloves, please get in touch. Direct from Korea.
PRoduct Name : Sars cov 2 (covid 19) igg/igm rapid test cassette Product Description : The ACtest COVID-19 IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG antinCoV-19 virus and IgM anti-nCoV-19 virus in human whole blood, serum or plasma. It is intended to be used by professionals as a screening test and as an aid in the diagnosis of infection with nCoV-19 viruses. The product has obtained the CE certification and is on the list of government export permits. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries. Price of product ( USD price or FOB price) : USD 3.5- USD 5 per test Product origin : Hangzhouï¼?Zhejiangï¼?China Key Specifications/Special Features : " Place of OriginHangzhouï¼?Zhejiangï¼?China Port Of Loading Shanghai Payment Term T/T Delivery Time Shipment within 7 working " Minimum Order Size and Packaging details Packing 40test/box, 25box/carton ,Minimum Order Quantity 1000test
I am the manufacturer of COVID-19 RAPID TEST in China. The ACtest COVID-19 IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-nCoV-19 virus in human whole blood, serum or plasma. It is intended to be used by the professionals as a screening test and as an aid in the diagnosis of infection with nCoV-19 viruses. The product has obtained the CE certification and is on the list of government export permits. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries.
We are a manufacturer of SARSCoV2 RAPID TEST CASSETTE in China. We can provide customers following SARSCoV2 rapid testing products that have obtained the CE or other certifications. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries. SARSCoV2 IgG/IgM Rapid Test Cassette SARSCoV2 Antigen Rapid Test (nasopharyngeal swab) SARSCoV2 Antigen Rapid Test (Saliva) SARSCoV2 and Influenza A+B Antigen Combo Rapid Test SARSCoV2 Neutralizing Antibody Test Kit
We are a manufacturer of SARSCoV2 RAPID TEST CASSETTE in China. We can provide customers following SARSCoV2 rapid testing products that have obtained the CE or other certifications. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries. SARSCoV2 IgG/IgM Rapid Test Cassette; SARSCoV2 Antigen Rapid Test (nasopharyngeal swab); SARSCoV2 Antigen Rapid Test (Saliva); SARSCoV2 and Influenza A+B Antigen Combo Rapid Test; SARSCoV2 Neutralizing Antibody Test Kit;
1. PROTAN COVID-19 IgM/IgG Protan Covid-19 IgM/ IgG is In-Vitro kit for the qualitative measurement of anti-COVID-19 IgM and IgG antibodies in human whole blood, plasma, and serum which non-medical professionals can use. It produces results in 15 minutes without additional analyzer and is for easy, simple and rapid test just with finger tip blood. 2. PROTAN COVID-19 IgG Type2 In-Vitro kit for the qualitative measurement of SARS-Cov-2 IgG antibodies against SP-RBD in human whole blood, plasma, and serum. Protan Covid-19 IgG Type2 neutralizing Antibody Rapid Test Kit is to check whether the formation of Covid-19 Neutralizing antibodies After vaccination. Protan Covid-19 IgG Type2 is intended for the detection of neutralizing antibodies(IgG) against Covid-19 SP RBD(spike protein-receptor binding domain) in Human whole blood after vaccination.
This kit is only used for the in vitro qualitative detection of 2019-nCoV antigen from human nasopharyngeal swab, nasal swab or oropharyngeal swab specimens. This kit is suitable for the auxiliary diagnosis of COVID-19, the results are for clinical reference only and cannot be used as the sole basis for diagnosis and exclusion decision. The clinical diagnosis and treatment of patients should be considered in combination with their symptoms/signs, medical history, other laboratory tests and treatment responses. Positive test result needs to be further confirmed, negative result does not preclude 2019-nCoV infection. This kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of in vitro diagnostic procedures. TEST PRINCIPLE The kit is immunochromatographic and uses double-antibody sandwich method to detect 2019-nCoV N protein antigen. During detection, the treated specimens are loaded into the sample wells of the test card. When the concentration of 2019-nCoV antigen in specimen is higher than the minimum detection limit, the viral antigen will form complexes with labeled antibodies first. Under chromatography, the complexes move forward along the nitrocellulose membrane till captured by pre-coated monoclonal antibody of 2019-nCoV in detection zone on nitrocellulose film (T) to form a pink/purple reaction line on the detection zone, at this point the result is positive; conversely, if there is no viral antigen or the concentration of antigen in specimen is below the minimum detection limit, no pink/purple reaction line appears in the detection zone, at this point the result is negative. Regardless of whether the sample contains viral antigens or not, a pink/purple reaction line will appear in the quality control zone (C), the pink/purple reaction line that appears in the quality control zone (C) is the criterion for determining if the chromatography process is normal.
Boson ART Test Kits MOQ: 100,000 kits
Flowflex ART Self-testing Kits MOQ: 100,000 kits
SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold Immunochromatography) Product Description SARS-COV2 Antigen Rapid Test Card contains a gold-labeled novel coronavirus N protein monoclonal antibody pre-coated on the bonding pad and a paired novel coronavirus N protein monoclonal antibodies �xed in the test line (T) and corresponding antibodies in the quality control line (C). SARS-COV2 Antigen Rapid Test Kit can detect the virus from the rst phase of infection (2-3 days before potential symptom onset) to the last phase of infection (7-10 days after potential symptom onset). Used to test COVID-19 antigen Card-like format detects the nucleocapsid (N) protein of the virus. Gold-labelled SARS-CoV-2 N protein monoclonal antibodies immobilized on the test area, with corresponding antibodies in the quality control area. Swabbed specimens from the nasopharynx or oropharyngeal, result in 15 minutes Product Features Non-invasive Simple to use Convenient, no devices required Rapid, get a result in 15 minutes Stable, with high accuracy Inexpensive, cost-efficiency Related News On 26th Jan 2021, report from PEI of an official test that The Federal Institute for Drugs and Medical Devices (Bundesinstitut fr Arzneimittel und Medizinprodukte, BfArM) authorized to perform, declared that Lepu Medical SARS-CoV-2 Antigen Rapid Test Kit has fulfilled all the minimum criteria for antigen tests conducted by PEI in consultation with the Robert Koch-Institut (RKI). In March 2021, German BfArM approved Lepu Medical SARS-CoV-2 antigen rapid test kit for home use. The test kit makes the coronavirus detection procedures rapid and easy.
We are supplier of ICMR approved ,CE Certified ,ISO certified pregnancy kit for detection of Pregnancy
We are supplier of ICMR,CE certified ,ISO certified test kit for detection of HIV 1,HIV 2
Advantages of the kits Antigen detection test ! Results in 15 to 30 minutes Only 100 µl of clinical sample needed (or 200 µl with dry swab sample) No PCR needed if positive results
Coronavirus IgG/IgM Dual Detection Kit: *****Just approved for marketing by Taiwan Food and Drug Administration, Ministry of Health and Welfare , It is the fastest (around 2-3 minutes) and the most accurate up to 97.3% comparing with global test kit. Made in Taiwan It can save the life because some hospitals require a confirmed test report ,then just will allow you to be hospitalized. Patients can get the fastest treatment and master the golden treatment time!!!
$6.00 from 10,000 pcs Commission: $0.10 mark up: allowed - 50% Seller/50% buyer Delivery: OTG New Jersey, USA Payment: 100% TT after inspection 1 box = 320 pcs
ExProbeTM SARS-CoV-2 qPCR Testing Kit EU CE Marked, US FDA EUA Approved, Taiwan FDA EUA Approved Intended Use: To detect RdRP/N/E RNA SARS-CoV-2 (COVID-19) in NP/O swabs and sputum. Product Format: 96 tests/kit Kit Contents: PCR Mix, Enzyme Mix, Pos. Control, Neg. Control and Instruction For Use. Storage / Stability: -20C + 5C / 6 months, repeat freeze thaw x 4. Testing kit is compatible for ABI7500,Roche 4800, TBG Q6000 qPCR Systems Reproducibility / Precision 100% Concordant across 3 lots with CV + 5% Limits of Detection (LOD) 50 copies/reaction Performance Comparison* Positive Samples 5 / 5 Negative Samples 199/200
SARS-CoV-2 Antigen Assay Kit (Colloidal Gold Method) This kit is used for the qualitative detection of specific antigen against novel coronavirus (SARS-CoV-2) in human specimens (Nasal swabs, oropharyngeal swabs, lower respiratory tract samples). Principle This kit adopts colloidal gold-based flow-through, lateral-flow immunoassay and capture method to detect specific antigen against coronavirus in human specimens(Nasal swabs, oropharyngeal swabs.
Product Description GeneTransport Medium Set - SG Medical Price of product ( USD price or FOB price) : USD2.4/set FOB Korea Product origin : REPURBLIC OF KOREA HS code 3821.00.0000 Key Specifications/Special Features : * For use in collecting, transporting and preserving salvia, oropharyngeal and nasopharynegeal specimens for the testing of respiratory pathogen * Increased testing accuracy: ^ Safe transport of samples by inactivation microbes and viruses ^ Visual checking of contamination using the indicator ^ 2 brushes for nasal and salvia samples * Stability of human body ^ Reduction of exposure to hazadous substances by using harmless water-based adhesive to attach brushess * Increased convenience ^ Automatic removal of brushes when the stopper is opened after transpoer * Storage method: unopened. At 18~25 deg.C for 12months after manufacturing Minimum Order Size and Packaging details : MOQ: 5000 sets
Product Description COVID-19 Ab Test - Boditech Price of product ( USD price or FOB price) : USD6.5/test FOB Korea Product origin : Republic Of Korea HS code 3822.00.1020 Key Specifications/Special Features : * Easy to use with small device * Fast and precise result (10mins) * Room temperatue storage * Anti-viral IgG / IgM test * Automated (AFIAS) or manual (iChroma II) platform * Assay type: TRFLFA*, IgM/IgG * Sample type: Whole blood / serum / plasma * Sample prep / extraction: Fingertip blood(C-tip)/ tube blood Certificates FDA, CE, ISO13485, FSC - MFDS * MFDS: Ministry of Food and Drug Safety of Korea Minimum Order Size and Packaging details : * MOQ: 1,000 tests * Packing: 24kits/box (AFIAS-1/6) 25kits/box (ichroma II)
