CTnI One Step Troponin I Rapid Test Kit (Whole blood/serum/plasma) 1.Product description Introduction: Product name: CTnI One Step Troponin I Rapid Test Kit Specification: Lateral-flow Immunofluorescence Chromatographic Assay 10 pcs, 25 pcs, 50 pcs, 100 pcs/box, or customized Type: Cassette MOQ: 10,000 PCS Analytical Range: 1.0~50ng/ml (Whole Blood); 0.1~50ng/ml (Serum/Plasma) Specimen: Human serum/plasma/whole blood Manufacturer: Hangzhou Laihe Biotech Co., Ltd. Clinical significance 1. Diagnosis of various chest pain 2. Foundation of ACS diagnosis and risk stratification 3. Best markers for ACS prognosis 4. An aid in the diagnosis of myocardial infarction (injury) 5. Can improve clinical, economic and operational outcomes Principle Insert the sample cassette into Immunofluorescence Quantitative Analyzer. The detection system will scan the markers and bond zone to gain optical signals, and then analyze the signals to get the concentration of the tested sample. Storage Valid for 24 months under 4-30 °C with aluminum foil bag packing. Once opened, the cassette is valid for 1 hour. 2.Application Clinical Laboratory, ED, ICU, CCU, Respiratory Department, Cardiology Department, Pediatrics Department, Surgery Department, Hematology Department, etc.
Multi-drug one step 2-15 drug test device (urine/saliva) 1.Product description 15.Png 20170120153542.Png Give a rapid diagnosis for reference to help in hospitals & clinics, rehabilitation centers, diseases control & prevention centers, military recruiting, high-risk group census, physical examination and some related special industries. Urine or saliva specimen to choose, easy specimen collection Instant result in 5 minutes Ce marked Valid for 24 months. Store at 2-30, 2.Features -choices: urine or saliva specimen for multi-drug test -test more than 2 drugs in one time, distinct c/t lines -customized sensitivity, printing color and packing -accurate, specific, quiet, stable, convenient -latest production -best seller in china domestic market, competitive quality and price -easy payment and shipment
Troponin I (CTnI) One Step Rapid Test Kit (Whole blood/serum/plasma) Product description Product name: CTnI One Step Troponin I Rapid Test Kit Specification: Lateral-flow Immunofluorescence Chromatographic Assay 10 pcs, 25 pcs, 50 pcs, 100 pcs/box, or customized Type: Cassette MOQ: 10,000 PCS Analytical Range: 1.0~50ng/ml (Whole Blood); 0.1~50ng/ml (Serum/Plasma) Specimen: Human serum/plasma/whole blood Manufacturer: Hangzhou Laihe Biotech Co., Ltd. 2.Clinical significance (1)Diagnosis of various chest pain (2)Foundation of ACS diagnosis and risk stratification (3)Best markers for ACS prognosis (4)An aid in the diagnosis of myocardial infarction (injury) (5)Can improve clinical, economic and operational outcomes
Tumor Marker PSA Prostate Specific Antigen Semi-Quantitative Rapid Test Strip Device Rapid Test Diagnostic Kit Accurate Product name: PSA Prostate Specific Antigen Semi-quantitative Rapid Test Kit Specimen: Whole blood/serum/plasma Format: Strip/cassette Specification: 25pcs, 40pcs, or customized MOQ: 10,000 pcs Sensitivity: 4ng/mL, 10ng/mL Application: Specific antigen in prostate, help in diagnosis of early prostatic diseases.
We can provide various infectious diseases test kits as listed. Product name Cat. No. Specimen Packing Chlamydia Rapid Test Device ICH-502 Swab/urine Cassette: 10 or 40pcs/box or Customized HBsAg One Step Hepatitis B Surface Antigen Test Device IHBsg-302 Serum/plasma Cassette: 10 or 40pcs/box or Customized HBsAg Hepatitis B Surface Antigen Rapid Test Device IHBsg-402 Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized HBsAg One Step Ultra Hepatitis B Surface Antigen Test Device IHBsg-302U Serum/plasma Cassette: 10 or 40pcs/box or Customized HCV Hepatitis C Virus Rapid Test Device IHC-302 Serum/plasma Cassette: 10 or 40pcs/box or Customized HCV Hepatitis C Virus Rapid Test Device IHC-402 Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized HIV 1/2 Antibody Rapid Test Device IHI-402 Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized H. Pylori Antigen Rapid Test Device IHPg-602 Feces Cassette: 10 or 40pcs/box or Customized H. Pylori Antibody Rapid Test Device IHPb-602 Serum/plasma Cassette: 10 or 40pcs/box or Customized Syphilis Ultra Rapid Test Device ISY-402U Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized Dengue Fever Rapid Test Device IDE-402 Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized Malaria P. f. /P. v. Rapid Test Device IMA-422 Whole blood Cassette: 10 or 40pcs/box or Customized
Product name: hCG One Step Pregnancy Test Kit,FSH One Step Menopause Rapid Test Kit ect. Specimen: Urine Format: Strip/cassette/midstream Specification: 25pcs, 40pcs, or customized MOQ: 10,000 pcs Accuracy: > 99% Storage: 4-30°C Valid for: 24 months
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
Product name:POCT PCT/CRP/hsCRP Rapid Test Kit Specification: 10 pcs, 25 pcs, 50 pcs, 100 pcs/box, or customized Specimen: Whole blood/serum/plasma Type:Cassette MOQ: 10,000 PCS Specimen:Human serum/plasma/whole blood Corollary machine: POCT Analyzer blood diagnostic machine FA-LF100B 2.Application PCT: Sepsis Monitoring 20170121143136.png Sepsis Diagnosis 20170121143156.png (Note: The cut-off value 2.0ng/ml is for reference only. Clinical departments shall adjust according to patient's situation.) CRP/hsCRP - Differential diagnosis of virus infection and bacterial infection - CRP relating with cardiovascular disease (CVD) - Accurate early diagnosis in pregnant women with amniorrhexis premature delivery and ch hsCRP < 1.0 mg/L Cardiovascular disease risk: Low risk 1.0-3.0 mg/L Cardiovascular disease risk: Moderate risk Anti-inflammatory therapy is recommended. > 3.0 mg/L Cardiovascular disease risk: High risk Anti-inflammatory and antithrombotic therapy is recommended. CRP < 10 mg/L Less possibility of bacterial infection or bacterium are eradicated 10-25 mg/L Virus infection signal When course is short, bacterial infection is possible. Re-check after hours. 25-50 mg/L Virus/bacterial infection signal 50-100 mg/L Usually bacterial infection Virus infection is uncommon. > 100 mg/L Bacterial infection signal Less possibility of virus infection
Product name: TORCH IgM Rapid Combo Test Device Format: Cassette Specimen: Whole blood/serum/plasma Test items: Toxo IgM, CMV IgM, Rubella IgM, HSV 1 IgM, and HSV 2 IgM Valid for: 24 months 2.Features -Customized sensitivity, printing color and packing -Accurate, quiet, stable, convenient -Latest production -Competitive quality and price -Easy payment and shipment
(1)The One Step Drug Screen Test Panel (Urine) is an immunoassay based on the principle of competitive binding.Drugs which may be present in the urine specimen compete against their respective drug conjugate for binding sites on their specific antibody. (2)During testing,a urine specimen migrates upward by capillary action. A drug, if present in the urine specimen below its cut-off concentration, will not saturate the binding sites of its specific antibody coated on the particles. The antibody coated particles will then be captured by the immobilized drug conjugate and a visible colored line will show up in the test line region of the specific drug strip. The colored line will not form in the test line region if the drug level is above its cut-off concentration because it will saturate all the binding sites of the antibody coated on the particles.
1.Product description (1)Product name: hCG One Step Pregnancy Test Kit (2)Specimen: Urine (3)Format: Strip/cassette/midstream (4)Specification: 25pcs, 40pcs, or customized (5)MOQ: 10,000 pcs (6)Accuracy: > 99% (7)Storage: 4-30°C (8)Valid for: 24 months
A rapid test for the qualitative detection of antibodies (IgG and IgM) to Dengue virus in whole blood, serum, or plasma. For professional in vitro diagnostic use only. INTENDED USE The Dengue IgG/IgM Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to Dengue virus in human whole blood, serum, or plasma as an aid in the diagnosis of primary and secondary Dengue infections. DIRECTIONS FOR USE Allow the test device, specimen, buffer, and/or controls to reach room temperature (1530°C) prior to testing. 1.Bring the pouch to room temperature before opening. Remove the test device from the sealed pouch and use it as soon as possible. 2.Place the test device on a clean and level surface. For Serum or Plasma Specimens: Hold the dropper vertically, draw the specimen up to the Fill Line (approximately 5 μL), and transfer the specimen to the specimen well (S) of the test device, then add 3 drops of buffer (approximately 90 L) and start the timer. See illustration below. Avoid trapping air bubbles in the specimen well (S). For Whole Blood (Venipuncture/Fingerstick) Specimens: To use a dropper: Hold the dropper vertically, draw the specimen 0.5-1 cm above the Fill Line, and transfer 1 drop of whole blood (approximately 10 µL) to the specimen well (S) of the test device, then add 3 drops of buffer (approximately 90 uL) and start the timer. See illustration below. To use a micropipette: Pipet and dispense 10 µL of whole blood to the specimen well (S) of the test device, then add 3 drops of buffer (approximately 90 µL) and start the timer. See illustration below. 3.Wait for the colored line(s) to appear. Read results at 10 minutes. Do not interpret the result after 20 minutes.
A rapid test for the qualitative detection of circulating antigens of Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae in whole blood. For professional in vitro diagnostic use only. Sensitivity The Malaria P.f/ Pan Rapid Test Device (Whole Blood) has been tested with thin or thick microscopy on clinical samples. The results show that the sensitivity of the Malaria P.f/ Pan Rapid Test Device (Whole Blood) is >99.9% relative to microscopy. For Pan: Relative Sensitivity: >99.9% (158/158) (97.6%100.0%)* For P.f: Relative Sensitivity: >99.9% (53/53) (93%100.0%)* Specificity The Malaria P.f/ Pan Rapid Test Device (Whole Blood) uses highly specific antibodies for Malaria P.f/ Pan antigens in whole blood. The results show that the specificity of the Malaria P.f/ Pan. Rapid Test Device (Whole Blood) is over 99.0% relative to microscopy. Relative Specificity: >99.0% (324/327)(97.3%99.8%)* Accuracy: >99.4%(535/538)(98.3%99.8%)* * 95% Confidence Interval Total Results211327538 Note: The comparison for Pan line has been only done with blood specimens positive with Plasmodium vivax specimen. The claims for Pan lines are based on scientific findings that Pan-malarial Aldolase is found in other malarial parasites including Plasmodium ovale and Plasmodium malariae.
In One Cup Cup Multi-drug One Step 2-15 Drug Test Simple Cup (Urine) CE Qualified (MOP/MET/KET/AMP/BAR/BUP/BZO/COC/COT/MDMA/THC/MTD/OPI/PCP/TCA)
Cardiac Marker CTNI Rapid Test Diagnostic Kit, Tumor Marker Test Kit, Infectious Diseases Diagnostic Test Kit, Fertility Rapid Test Kit, Torch IgM Rapid Combo Test Device.Shipping
Covid-19 Self Test Kit We are the authorized first vendor of ADTech! KFDA CE approved, FDA Pending Price : Negotiable Pre-Clinical Test Report Accuracy - In total samples 93.3% (14/15) - In positive samples 91.7% (11/12) 1. Pre-Clinical Test summary 1) Pre-clinical test is fulfilled by Domestic large clinical laboratory with ADTech COVID-19 IgM/IgG RAPID KIT 2) Tests are made by total 15 samples with 12 positive and 3 negative samples 3) Clinical Laboratory tested the sample with Immunofluorescence Analysis 2. Pre-clinical test result 1) Samples were tested by ADTech COVID-19 IgM/IgG RAPID KIT 2) Test result by ADTechs RAPID KIT - 4 negatives and 11 positives results in 15 samples 3) Comparison between Immunofluorescence analysis and ADTechs RAPID KIT - 14 test results are same(including negative and positive results) - 1 samples test result are different(Positive Negative by ADTech