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High Accuracy Urine Doa Multi Panel Drug Test Cassette Strip
US$0.20
1,000-9,999,999 Pieces
US$0.01
10,000,000+ Pieces
Product specifications
CM
Product profile
Customization
AvailableClassification
Biological DiagnosticsType
Urine AnalyzerModel NO.
Drug of AbuseCertification
CE, FDA, ISO13485, SGSGroup
Middle-aged and OldCheap Price
0.01--0.2Cutoff
100%ISO
TUV CertifiedCE
TUV CertifiedFDA
510KSensitivity
HighMOQ
1000Read Time
Within 10 MinutesBrand Name
HighplusOEM
AcceptableODM
AcceptableSample
AcceptableStorage
4-30℃Advantage
Fast and Easy to UsePower Source
ElectricTransport Package
Individual Foil Pouch/ Customized PackageSpecification
Customized PackageTrademark
OEMOrigin
ChinaHS Code
3002190090Production Capacity
200000PCS/WeekKey features
High Sensitivity and Accuracy: Utilizes Colloidal Gold Method for excellent sensitivity, specificity, and accurate qualitative detection.
Fast and Easy Operation: One-step lateral flow immunoassay with results readable within 10 minutes and simple interpretation.
Comprehensive Certifications: Certified by CE, FDA (510K), ISO13485, TUV, and SGS for global compliance and safety.
Flexible Customization Options: Accepts OEM, ODM, and custom sample requests with adjustable cutoff concentrations.
Diverse Packaging Solutions: Offers bulk pouch packing or individual box packaging to meet pharmacy and strict regulatory requirements.
Rapid Response Service: Dedicated staff resolves product issues within 24 hours with quick and decisive support.
Stable Storage Conditions: Maintains product integrity with a storage temperature range of 4-30 degrees Celsius.
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's the method u use to do the test?
A:
Colloidal Gold Method.
Q:What's ur MOQ ?
A:
Always, for strip format, the MOQ is 5000pcs. While for cassette format, MOQ is 2000pcs, same as midstream.
Q:What's ur packing of the tests?
A:
If u choose the low cost, we will suggest u the bulk packing to go. Which means 1 test in a single pouch, then 100/40 pouches in a plastic bag, 50 bags in a carton. If u need to sell in pharmacy/chain shop or some countries which have strict requirements about the packing, u can choose to pack in a box, like 100pcs in a box, or even 1 test in a single box.
Q:What's the main differences when comparing products from different suppliers?
A:
U can compare the mainly features of the test: Accuracy, Sensitivity, Specificity, and then the Price.
Q:Some tests can be tested with serum/plasma or with whole blood, so what's the difference?
A:
Well, if the specimen is whole blood, people will need buffer, lancet and alcohol swab to help the test. If they buy all the accessories, they can test very easily at home. But if the specimen is serum/plasma, it will need centrifuge to separate serum from whole blood first. This way, it's better to use at lab or hospital. And in some words, serum/plasma test will always give a 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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