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Factory Direct Supply HIV Test Kit for Serum Whole Blood Specimen Detection
US$0.20
10,000-999,999 Pieces
US$0.01
1,000,000+ Pieces
Product specifications
CM
Sample price:US$0.50/piece.Request sample
Product profile
Customization
AvailableClassification
Biological DiagnosticsType
HIV Rapid TestModel NO.
HIV-W11/W23/W23HCertification
CE, FDA, ISO13485Group
AllCheap Price
0.01--0.2Cutoff
100%ISO
TUV CertifiedCE
TUV CertifiedFDA
510KMOQ
1000Sensitivity
HighRead Time
Within 10 MinutesBrand Name
HighplusOEM
AcceptableODM
AcceptableSample
AcceptableAdvantage
Fast and Easy to UseStorage
4-30℃Power Source
ElectricTransport Package
Individual Foil PouchSpecification
CassetteTrademark
OEMOrigin
ChinaHS Code
3002190090Production Capacity
500000000PCS/YearKey features
CE, FDA, ISO13485 Certified: Obtained CE, FDA 510K, and ISO13485 certifications for quality assurance.
High Sensitivity & Accuracy: Employs sandwich dye conjugate immunoassay for excellent sensitivity and specific results.
Fast & Easy to Use: Simple steps with easy interpretation; results available within 10 minutes.
OEM & ODM Acceptable: Customization services including OEM and ODM are available for branding needs.
Multiple Specimen Types: Compatible with serum, plasma, and whole blood for versatile testing scenarios.
24-Hour After-Sales Support: Dedicated staff responds to product issues or dissatisfaction within 24 hours.
Company profile

CertifiedBusiness Type: Trading CompanyExport Year: 2018-05-30 CertifiedNearest Port: Qingdao PortAverage Response Time: ≤1.73h 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 employs the Colloidal Gold Method using sandwich dye conjugate immunoassay.
Q:What is the MOQ for different formats?
A:
For strip format, the MOQ is 5000pcs. For cassette format, the MOQ is 2000pcs.
Q:What are the packing options?
A:
Options include bulk packing (1 test in pouch, 100/40 pouches in bag, 50 bags in carton) or box packing (100pcs/box or single box) for strict requirements.
Q:What is the difference between serum/plasma and whole blood tests?
A:
Whole blood requires buffer, lancet, and alcohol swab for home use. Serum/plasma requires centrifugation, making it better for labs/hospitals, and generally provides more accurate results.
Q:How to distinguish a good test kit?
A:
Check technical data (accuracy, specificity, sensitivity), pouch sealing tightness, flow speed (not too fast), and background cleanliness after running.
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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