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Influenza a+B AG Rapid Test Kits
US$0.20
1,000-9,999 Pieces
US$0.10
10,000+ Pieces
Sample price:US$0.00/piece.Request sample
Product profile
Customization
AvailableClassification
Biological DiagnosticsType
Urine AnalyzerModel NO.
FLU-S23Certification
CE, FDA, ISO13485Group
Middle-aged and OldTransport Package
Individual Foil Pouch/ Customized PackageSpecification
Customized PackageTrademark
OEMOrigin
ChinaHS Code
3002190090Production Capacity
200000PCS/WeekKey features
High Accuracy Rate: Provides >99% accuracy for rapid differential diagnosis of influenza A and B.
Fast Results: Results can be read at 10 minutes with a maximum interpretation time of 20 minutes.
Multiple Formats: Available in cassette formats with 4.0mm and 5.0mm widths to suit different needs.
CE, FDA, ISO13485 Certified: Product holds CE, FDA, and ISO13485 certifications for quality assurance.
Customizable Design: DAG design or customized according to customer requirements.
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:
Colloidal Gold Method.
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 a pouch, 100/40 pouches in a bag, 50 bags in a carton) or box packing (100pcs in a box or 1 test in a single box) for strict requirements.
Q:How to distinguish a good test kit?
A:
Judge by technical data (accuracy, specificity, sensitivity), pouch sealing tightness, flow speed, and background cleanliness.
Q:What is the difference between whole blood and serum/plasma tests?
A:
Whole blood tests require buffer, lancet, and alcohol swab for home use. Serum/plasma tests require centrifugation and are better for labs/hospitals, often providing more accurate results.
Send Inquiry
*To:Shandong Highplus Biotech Co., Ltd.
Shandong Highplus Biotech Co., Ltd.*Content:
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