How long does it take to get results?

Results can be read within 10 minutes. The reaction requires sufficient time for antibodies to work, so refer to the instruction for accurate timing.

What certifications does the product have?

The product is certified by CE, FDA (510K), ISO13485, SGS, and TUV.

Premium Urine Doa Multi Panel Drug Abuse Test Strip Cassette

Name: Premium Urine Doa Multi Panel Drug Abuse Test Strip Cassette
Brand: Shandong Highplus Biotech Co., Ltd.
SKU: 2139779432

Shandong, ChinaShandong Highplus Biotech Co., Ltd.

US$0.20

1,000-9,999,999 Pieces

US$0.01

10,000,000+ Pieces

Product specifications

CM

Sample price:US$0.00/piece.Request sample

Product profile

Customization

Available

Classification

Biological Diagnostics

Type

Urine Analyzer

Model NO.

Drug of Abuse Tests

Certification

CE, FDA, ISO13485, SGS

Group

Middle-aged and Old

Cheap Price

0.01--0.2

Cutoff

100%

ISO

TUV Certified

CE

TUV Certified

FDA

510K

Sensitivity

High

MOQ

1000

Read Time

Within 10 Minutes

Brand Name

Highplus

OEM

Acceptable

ODM

Acceptable

Sample

Acceptable

Storage

4-30℃

Advantage

Fast and Easy to Use

Power Source

Electric

Transport Package

Individual Foil Pouch/ Customized Package

Specification

Customized Package

Trademark

OEM

Origin

China

HS Code

3002190090

Production Capacity

200000PCS/Week

Key features

High Sensitivity & Accuracy: Utilizes Colloidal Gold Method for excellent sensitivity and clean background results.

Fast & Easy Operation: One-step lateral flow immunoassay with results readable within 10 minutes.

Flexible Customization: Accepts OEM/ODM services with customizable cutoff concentrations and packaging.

Global Certifications: Certified by CE, FDA (510K), ISO13485, SGS, and TUV for quality assurance.

24-Hour After-Sales Support: Dedicated staff responds to product issues within 24 hours of receipt.

Multiple Format Options: Available in Strip, Cassette, and Cup formats with 2-18 drug combinations.

Competitive Pricing: Offers cheap price options with bulk packing to reduce costs for buyers.

Company profile

Shandong Highplus Biotech Co., Ltd.

Shandong, China

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?

The test uses the Colloidal Gold Method, a lateral flow one-step immunoassay.

Q:What is the MOQ for different formats?

For strip format, the MOQ is 5000pcs. For cassette and midstream formats, the MOQ is 2000pcs.

Q:What are the packing options?

Options include bulk packing (1 test in pouch, 100 pouches in bag, 50 bags in carton) or boxed packing (100pcs/box or 1 test/box) for strict retail requirements.

Q:How to distinguish a good test kit?

Check technical data (accuracy, specificity, sensitivity), pouch sealing tightness, flow speed, and background cleanliness. Avoid kits with red smears which indicate bad technology.

Q:What is the difference between urine, serum/plasma, and whole blood tests?

Urine tests are simple. Whole blood tests require buffer and lancets for home use. Serum/plasma tests require centrifugation and are better for labs/hospitals, offering higher accuracy.