HCG Pregnancy Test - CE & FDA Approved
HCG test kits is a rapid test to detect the presence of HCG in urine or serum specimens in a qualitative format sensitive to 20mIU/ml. The test utilizes a combination of monoclonal and polyclonal antibody reagents to selectively detect elevated level of HCG in urine or serum. The immunological specificity of the test virtually eliminates cross reactivity interferences from the structurally related glycoprotein hormones hFSH, hLh, hTSH at physiological levels. Specification: 3. 0mm, 4. 0mm, 5. 0mm or according to customers requirements. Packing details: Midstream: 20pcs/box, 30boxes/carton. Cassette: 40pcs/box, 50boxes/carton. Strip: 100pcs/bag, 100bags/carton Container loading: Midstream: 250,000pcs/20FT container. Cassette: 500,000pcs/20FT container. Strip: 1,300,000pcs/20FT container.
Product Name Human Chorionic Gonadotropin (HCG) Test Kit (Immunofluorescence Chromatography) Purpose To detect the content of HCG in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only. Principles of Detection The HCG Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing HCG antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HCG antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody). HCG concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of HCG according to the preset calibration curve in the machine and display the result, detection unit is mIU/mL. C line should appear in any cases, which indicates the reaction system is effective. Storage conditions and shelf life Store in a sealed aluminum foil bag at 2 - 30 C. After unpacking the aluminum foil bag under temperature 20~30 C , humidity 35~65%, please use it immediately. Shelf life 18 months. Applicable instrument Avid fluorescent immunoanalyzer model: AI-IF 600
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
Initial pregnancy gold gel reagent (one step hcg pregnancy test strip) Explanation of the test One step hcg pregnancy test strip (urine) is a rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin (hcg) in urine to aid in the early detection of pregnancy. Human chorionic gonadotropin (hcg) is a glycoprotein hormone produced by the developing placenta shortly after fertilization. In normal pregnancy, hcg can be detected in both urine and serum as early as 7 to 10 days after conception (1-4). Hcg levels continue to rise very rapidly, frequently exceeding 100 miu/ml by the first missed menstrual period (2-4), and peaking in the 100, 000-200, 000 miu/ml range about 10-12 weeks into pregnancy. The appearance of hcg in both urine and serum soon after conception, and its subsequent rapid rise in concentration during early gestational growth, making it an excellent marker for the early detection of pregnancy. One step hcg pregnancy test strip (urine) is a rapid test that qualitatively detects the presence of hcg in urine specimens at the sensitivity of 20 miu/ml. The test utilizes a combination of monoclonal and polyclonal antibodies to selectively detect elevated levels of hcg in urine. At the level of claimed sensitivity, one step hcg pregnancy test strip (urine) shows no cross-reactivity interference from the structurally related glycoprotein hormones hfsh, hlh and htsh at high physiological levels. 50 tests pack.
CE Approved The human Chorionic Gonadotropin (HCG) Pregnancy Test Kit is a rapid, one-strip lateral flow immunoassay for the qualitative determination of HCG in human urine specimens, to aid in the early detection of pregnancy. Advantage: Simple to use, no need for additional equipment, qualitative result in 2-5 minutes 10-25mlU/mL sensitivity Over 99% accuracy OEM service
Our product is based on the theory of enzyme interaction. It is used to detect the HCG atom in urine speciment. The colour change could identify the test result directly. Assisting with the result,doctor could judge whether the patient is pregnant or not. 2.5mm, 200 strips/pouch, 10,000strip /case ,27kg 3.0mm, 50 kits/ pouch, 2,000 kits/case, 27kg 4.0mm, 150 cards/pouch, 2,500 cards/case, 25kg 5.0mm 10000strips/case 2000kits/case 2500cards/case.
HCG Pregnancy rapid test Home Test CE approved Strip , Cassette , Midstream 10miu ,25miu. 2.5mm, 200 strips/pouch, 10,000strip /case ,27kg 3.0mm, 50 kits/ pouch, 2,000 kits/case, 27kg 4.0mm, 150 cards/pouch, 2,500 cards/case, 25kg 5.0mm 10000strips/case 2000kits/case 2500cards/case.
Hello, we are a manufacturer in China. There are 40,000 square meters of factory Welcome friends to visit If you want to buy, please contact us thanks A single-use self-diagnostic pregnancy test. This test is used to qualitatively detect HCG (human chorionic gonadotropin) in urine for early detection of pregnancy. Model: strip, cassette, midstream Effective rate: 99.98%. Inner strip width: 3mmï¼?4mmï¼?6mm. Sensitivity: 25ml/miu Liquid moving speed: 10mm/ml Certificate: CE, ISO13485 Support small batch export Support mass customization Support exporting large boards Contact us for detailed pricing Looking forward to your contact
Hcg rapid diagnostics test kits(ce & iso)
The CorDx HCG PREGNANCY TEST MIDSTREAM KIT FOR SELF TESTING is a rapid test for the qualitative detection of human chorionic gonadotropin (hCG) in urine species to aid in the early detection of pregnancy. It is intended for home users and for prescription use. Featuresï¼? accuracy>99.5% sensitivity: 25miu /ml rapid: result is readable as quick as in 1 minute. specimen: urine, widely used for self-testing. shelf life: 36months or 24months packing:1pc/box, 3pcs/box CE and FDA approved
Rapid HCG Pregnancy Test Card Intended Use HCG Pregnancy Urine Test is a chromatographic immunoassay for the early detection of human chrionic gonadotropin (HCG) in urine specimens. Contents of Kit HCG Pregnancy Test Card 25 ea Instructions For Use 1 ea Storage And Stability The kits should be stored at temperature 4-30ípC in the sealed pouch for the duration of the shelf life. Pre Cautions 1. For in vitro diagnostic use only. 2. Do not use after expiration date. 3. Test device should remain sealed until use. 25 tests/kit, 40 kits/carton
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
COVID-19 Rapid Test Kit IgG + IgM (Colloidal Gold) comes in packs of 40 tests and contains: GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request. To get over COVID-19 pandemic, especially the recent Omicron breakout, currently we are doing big promotions for three kinds of COVID-19 Ag kit. All are in stock and available right away. 1. Nasopharyngeal 2. Nasal 3. Saliva Price and Minumum Quantity Price FOB in USD: negotiable 0.8 to 1.8Minimum Order Qty: None Pieces Production Capacity: 3,000,000/monthPackaging: 20 Tests/kit, 30 Kits/box, 12 Boxes/pallet Sample: Available. Sample Cost Born By Supplier Product Model And Origin Brand: GENEDIAModel: 643G-S (Saliva) Seller Code: Genedia w covid 19 agHS Code: 3002.15 Standards: Ce Competitive Advantages Allow wider testing with fast test time (10 minutes) All necessary materials provided / no equipment needed Sensitivity: 93.33%, specificity: 100% Free sample. no moq. price is negotiable. customized packing. Other Details 20 tests / kit 24 months from the date of manufacture 2 ~ 30c(35.6 ~ 86f) available for room temperature deliver In stock. fast delivery. 1 x Instructions for Use Manual 40 x Test Cassettes 1 x Buffer 40 x Dropper
Angiten-COVID-19 Virus Test Kit (Colloidal Gold) Quantity of box: 25 persons/box Brand: Easysweet NMPA (National Medical Products Administration): Approved CE: with CE mark BfArM: listed Test Method: Antigen Test Result Time: 10-15 mins Sample Type: Nasal Swab Sensitivity: 96.70% Specificity: 100% Accuracy: 98.94% Shelf Life: 24 months Storage Temperature: 2-30 Degree Celsius Country of Origin: Made in China Additional Information: Production Capacity: 1 million Delivery Time: 10-15 days Packaging Details: 25 tests in a pack, 40packs/ carton Angiten-COVID-19 Virus Test Kit is an in vitro diagnostic rapid test for the qualitative detection of SARS-CoV-2 antigen (Ag) in human nasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. It can be used by professional only. Price and Minumum Quantity Price FOB in USD: NegotiableMinimum Order Qty: 10000 Production Capacity: 1000000Packaging: 25 Persons/box Sample: Available. Sample Cost Born By Buyer Product Model And Origin Brand: Easysweet HS Code: 3822009020 Standards: Ce Competitive Advantages Best price with shortest delivery time Best price with shortest delivery time Best price with shortest delivery time Best price with shortest delivery time Other Details Angiten-covid-19 virus test kit (colloidal gold) Angiten-covid-19 virus test kit (colloidal gold) Angiten-covid-19 virus test kit (colloidal gold) Angiten-covid-19 virus test kit (colloidal gold)
Covd-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) is a solid phase immunochromatographic assay for the rapid, qualitative and dierential detection of IgG and IgM antibodies to 2019 Novel Corona Virus in human whole blood, serum or plasma. Specification.jpg Product: Rapid Diagnostic Test Kit Item: Corona Virus Test Kit Specimen: Whole Blood/Serum/Plasma Format: Strip/Cassette Port of Loading: Shanghai OEM and ODM: OEM/ODM Welcome Shipping: By UPS, FEDEX, DHL, TNT, by air or by sea MOQ for Private label: Low MOQ 1600 boxes, Please contact us. Note: Store this product in a cool and dry place, avoid direct sunlight, stay away from places that children can contact, and avoid eye contact. If you have allergies to this product, please stop using and consult a doctor. COVID-19 Corona Virus Rapid Test Kit11.pngCOVID-19 Corona Virus Rapid Test Kit12.png
Access Bio Care Start Covid-19 Rapid Antigen Test Kit Product Details: Number of Reactions(Preps) per Kit : 1 Brand : Access Bio Test Method : Antigen Test Result Time (Rapid Kits) : 10 min Sample Type ; Nasal Swab Packaging Size : 20 Test Kits/Box Packaging Type : Box The CareStart COVID-19 Antigen test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals who are either suspected of COVID-19 by their healthcare provider within first five days of symptom onset, or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between