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Standard Specification HCG Test Kit for Urine Pregnancy Rapid Detection Work
US$0.20
1,000-999,999 Pieces
US$0.01
1,000,000+ Pieces
Product specifications
CM
Sample price:US$0.00/piece.Request sample
Product profile
Customization
AvailableClassification
Biological DiagnosticsType
Urine AnalyzerModel NO.
HCG-U23Certification
CE, FDA, ISO13485Group
Middle-aged and OldSpecimen
Urine / SerumMethodology
Colloidal Gold Immune Chromatographic AssayStorage
4-30℃OEM
AcceptableODM
AcceptableSample
AcceptableAdvantage
Fast and Easy to UseResult
5 MinutesMOQ
1000Lead Time
30 DaysAffordable Price
0.2-0.01Transport Package
Individual Foil Pouch/ Customized PackageSpecification
Customized PackageTrademark
OEMOrigin
ChinaHS Code
3002190090Production Capacity
200000PCS/WeekKey features
High Accuracy Rate: Over 99% accuracy ensures reliable pregnancy detection results.
Rapid Result Reading: Get clear results within 5 minutes for quick decision making.
Multiple Formats Available: Choose from strip, cassette, or midstream formats to suit needs.
Flexible Customization: OEM, ODM, and sample services are acceptable for customization.
Certified Quality: Products hold CE, FDA, and ISO13485 certifications for safety.
Long Shelf Life: 3 years shelf time ensures product stability and usability.
Sensitive Detection: High sensitivity levels of 10miu, 20miu, or 25miu available.
Versatile Specimen Types: Compatible with both urine and serum specimens for testing.
Company profile

CertifiedBusiness Type: Trading CompanyExport Year: 2018-05-30 CertifiedNearest Port: Qingdao PortAverage Response Time: ≤1.90h CertifiedTerms of Payment: T/T, D/P, PayPal, etc. CertifiedInternational Commercial Terms(Incoterms): FOB, CIF, CFR
AI-Powered supplier vetting
SummaryShandong Highplus Biotech Co., Ltd. is a China-based limited company in Weifang, Shandong, identified as both a trading company and manufacturer/factory focused on in vitro diagnostic reagents and POCT-related products. It reports ISO 13485 and ISO 9001 management-system certifications and states that most products have CE, CFDA, FDA, and Free Sale Certificates, although product-specific verification is not provided. The supplier reports more than 10 production lines, 11–20 years of R&D engineer experience, 6–10 quality-control staff, export sales accounting for 90% of total sales, and markets spanning multiple regions. Delivery is stated as within 15 workdays in both peak and off-peak periods. The evidence does not establish after-sales service capability, customization capability, or customer cases. Financial information is not assessed because monetary figures are excluded.
Supplier typeThe supplier is explicitly classified as both a trading company and manufacturer/factory. Its stated business focuses on in vitro diagnostic reagents, POCT analyzer-related products, rapid test kits, test strips, analysis equipment, and related materials, with a factory location identified in Weifang, Shandong.
CertificationsThe supplier explicitly reports ISO 13485 and ISO 9001 certifications for its management systems. It also states that most products have CE, CFDA, FDA, and Free Sale Certificates, but the supplied information does not identify certificate numbers, validity periods, or product-specific coverage.
R&D capabilityThe supplier states that it develops or supplies in vitro diagnostic reagents, POCT analyzer-related products, chemiluminescent immunoassay reagents, and bioactive materials. It reports 11–20 years of R&D engineer experience, which supports an established technical resource base, but no evidence is provided on patents, new-product launches, dedicated R&D investment, or proprietary technologies.
Production capacityThe supplier reports more than 10 production lines, 6–10 quality-control staff, and order fulfillment within 15 workdays during both peak and off-peak seasons. It also exports to multiple global regions and identifies factory premises in Weifang, indicating established manufacturing and international fulfillment capacity.
Product Q&A
Q:What testing method is used?
A:
The test uses the Colloidal Gold Method for detection.
Q:What is the MOQ for different formats?
A:
For strip format, the MOQ is 5000pcs. For cassette and midstream formats, the MOQ is 2000pcs.
Q:What packaging options are available?
A:
Options include bulk packing (single pouch in plastic bag in carton) or boxed packing (e.g., 100pcs per box) for stricter retail requirements.
Q:How to distinguish a good test kit?
A:
Evaluate technical data (accuracy, specificity, sensitivity), pouch sealing tightness, flow speed, and background cleanliness after running.
Q:What is the difference between serum/plasma and whole blood tests?
A:
Whole blood tests require buffer, lancet, and alcohol swab for home use. Serum/plasma tests require centrifugation, making them better for labs/hospitals, and generally provide more accurate results.
Send Inquiry
*To:
Shandong Highplus Biotech Co., Ltd.
Shandong Highplus Biotech Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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