Human Chorionicgonadotropin HCG Card Pen Midstream Urine Serum Pregnancy Rapid Test
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Product Highlights
- Rapid Result Time: Provides qualitative results within 3 to 5 minutes for quick pregnancy detection.
- Multiple Specimen Types: Compatible with both urine and serum specimens for versatile testing options.
- OEM and ODM Services: Offers full OEM and ODM customization services for brand and product requirements.
- CE Certified Quality: Manufactured under CE certification standards ensuring reliable in vitro diagnostics.
- Flexible Packaging Options: Available in 1, 40, or 100 tests per box to suit different usage needs.
- Professional Grade Accuracy: Uses immunochromatography principle for accurate detection of human chorionic gonadotropin.
Product Attributes
- Customization
- Available
- Certificate
- Ce
- Component
- Rapid Test
- Model NO.
- HCG
- Specimen
- Urine/Serum
- Result Time
- Within 3 Mins
- Storage
- 2~30 ℃
- Principle
- Immunochromatography
- Shelf Life
- 24 Months
- Transport Package
- 100tests/Box, 40tests/Box, 1test/Box
- Specification
- 1000tests/Carton
- Trademark
- Dewei
- Origin
- China
Product Images of Human Chorionicgonadotropin HCG Card Pen Midstream Urine Serum Pregnancy Rapid Test
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Product Description
INTENDED USE
For in vitro self test use only.
| Storage | 2~30 º C |
| Specimen | Urine/Serum |
| Component | Rapid Test + Pipettes |
| Principle | Colloidal gold rapid tests |
| Reading | Within 5mins |
| Package | 40tests/box |
| Trademark | Dewei |
| Origin | China |
PRINCIPLE
Human chorionicgonadotropin (hCG), a glycoprotein hormone secreted by viable placental tissue during pregnancy, is excreted in urine approximately 20 days after the last menstrual period. hCG levels rise rapidly, reaching peak levels after 60-80 days. The appearance of hCG in urine soon after conception and its rapid rise in concentration makes it an ideal marker for the early detection and confirmation of pregnancy. However, elevated hCG levels are frequently associated with trophoblastic and non-trophoblastic neoplasms and hence these conditions should be considered before a diagnosis of pregnancy can be made.
The hCG Rapid Test detects human chorionicgonadotropin through visual interpretation of color development on the strip. Anti-hCG antibodies are immobilized on the test region of the membrane and anti-mouse antibodies on the control region. During testing, the specimen reacts with anti-hCG antibodies conjugated to colored particles and precoated onto the sample pad of the strip. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there is sufficient hCG in the specimen, a colored band will form at the test region of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
WARNINGS AND PRECAUTIONS
Immunoassay for in vitro diagnostic use only.
Do not use after expiration date.
The test should remain in the sealed pouch until use.
The used test should be discarded according to local regulations.
STORAGE AND STABILITY
The kit should be stored at 2-30°C until the expiry date printed on the sealed pouch.
The test must remain in the sealed pouch until use.
Keep away from direct sunlight, moisture and heat.
Do not freeze.
Care should be taken to protect the components of the kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipment, containers or reagents can lead to false results.
OPERATION
Bring tests, specimens, and/or controls to room temperature (15-30°C) before use.
1. Remove test Strip, Device or Midstream from the sealed pouch.
2.1 Strip:
container with urine sample, take it out in 5
seconds and lay flat.
2.2 Device/Cassette:
Remove test device/cassette from the sealed pouch.Lay the device flat, add 2-3 drops of urine
specimen by sample dropper into the sample well.
2.3 Midstream/Pen:
Remove test midstream from the sealed pouch.
Open the midstream cup, dip the sample collection
head into urine sample, take it out in 5 to 10
seconds and lay it flat.
3. Read the results within 5 minutes.
POSITIVE: 2 colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).
NEGATIVE: Only 1 colored band appears, in the control region (C). No colored band appears in the test region (T).
INVALID: Control band fails to appear. Results from any test which has not produced a control band at the specified read time must be discarded. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.
PRODUCT IMAGE
Midstream Pen Device Cassette Strip Dipstick
R&D TEAM
PRODUCTION LINE
CERTIFICATES
EXHIBITIONS 
SHIPMENTS 
About the Supplier
This supplier has been audited by BV. Verify the report on the official BV website with ID "MIC-ASI2211915". Items marked "" are certified.
Company Profile
Dewei Medical Equipment Co., Ltd. is a high-tech enterprise specialized in developing and marketing of Medical Consmuables like Rapid Test Kits, Hematology Analyzer Reagents, Virus Transport Medium and DNA RNA Extraction Kits.
Rapid Test type of Infectious Disease, Drug of Abuse, Cardiac Markers, Tumor Markers and Fertility parameters, Packing type of Caseette, Strip and Cup, Specimen type of Urine, Blood, Swab and Feces.
Dewei products are widely used in hospital clinics, disease control centers, blood banks, veterinary clinics, scientific research center and college laboratories.
Quality is our primary concern, Dewei team is strict on quality control systems thus most of our products got CE, ISO, and other international standards certificates. No defective is allowed under this procedure.
With professional R&D team, Dewei is continuously making new achievements on innovation, gaining numbers of national invention patents and professional technical awards. Meanwhile, Dewei focuses on the improvement of technology to guarantee product quality and pursue product performance.
By flexible Production management, Dewei has automated production line, stock alarm would be set every month, thus sufficient capacity can support customer inquiry.
The view of Dewei is to be the most professional and respected enterprise in medical field, Dewei will go on providing best service to you by the outstanding R&D and cost-effective products. Only win-win is the real victory, we are willing to grow together with you.
About Our Factory & Business Background
-
Business Type
- Manufacturer/Factory & Trading Company
- Address
- 5th Floor, Building 14, Shiyou Industrial City, No. 194 Junyi Road, Jun'an Town, Shunde District, Foshan City, Guangdong Province
-
Plant Area
- 2266 square meters
-
Number of Employees
- 50
-
Registered Capital
- 5,000,000 RMB
-
Terms of Payment
- LC, T/T, D/P, PayPal, Western Union, Small-amount payment
-
International Commercial Terms(Incoterms)
- FOB, CIF, CFR, EXW
-
Average Lead Time
-
Peak Season Lead Time: within 15 workdays
Off Season Lead Time: within 15 workdays -
Nearest Port
- Guangzhou Port, Shenzhen Port, Foshan Port
Our Production Capability & Technical Expertise
-
Main Products
- Hematology Reagents, Rapid Test for Fertility, Drug of Abuse, Infectious Disease, Cardiac Markers and Tumor Markers
-
Production Machines
- Allegra 64R Centrifuge, Auto F.P Osmometer, Automatic NC Film Gluing Facility, Conductivity Meter, Continuous Film Splitter, Hair Drug Detector, Hemocytometer, Sheet Cutting Facility, Ultrasonic Homogenizer
-
ODM Service Available
- Yes
-
OEM Service Available
- Yes
-
R&D Engineers
- 10 people
-
Test Reports for Raw Materials
- Others
-
Own Brand
- Yes
Our Industry Experience & Global Business Record
-
Year of Establishment
- 2020-08-03
- Export Year
- 2017-09-01
-
Main Markets
- North America, South America, Europe, Southeast Asia/ Mideast, Africa, Domestic
-
Number of Foreign Trading Staff
- 8
-
Overseas Agent/Branch
- No
Our Certifications, Standards & Industry Recognition
-
Product Certification
- CE
FAQ
- How long does it take to get results?
- Results can be read within 3 to 5 minutes after applying the specimen.
- What types of samples can be used?
- The test is designed for use with human urine or serum specimens.
- Is OEM or ODM service available?
- Yes, the manufacturer offers both OEM and ODM services for customization.
- What does a positive result look like?
- A positive result shows two colored bands: one in the control region (C) and one in the test region (T).
- What certifications does the product have?
- The product is CE certified for in vitro diagnostic use.
- What are the payment terms?
- Accepted payment methods include LC, T/T, D/P, PayPal, Western Union, and small-amount payments.
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