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DOA Drug Test

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DOA Drug Test
Details
DOA Drug Test Device
Multiplex Substance Screening: Simultaneously identifies up to distinct drug metabolites and chemical adulterants within a single non-invasive urine specimen, streamlining clinical toxicological diagnostics.
Tamper-Evident Security System: Engineered by Hangzhou Lysun Biotechnology with integrated temperature verification strips and built-in sample adulteration detection wells to prevent fraudulent substitution.
Global Factory-Direct Sourcing: As an ISO 13485 certified IVD manufacturer, we empower international medical channels and procurement groups with competitive bulk pricing and flexible OEM private labeling.
Category
AMP Test
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Description
Product Overview & Clinical Value
The DOA Drug Test panel stands as a premier point-of-care (POCT) screening asset designed for comprehensive toxicological evaluations, forensic diagnostics, and occupational safety compliance. Developed and manufactured by Hangzhou Lysun Biotechnology using advanced lateral flow competitive immunochromatography, this professional-grade multiplex screening diagnostic kit allows healthcare providers and law enforcement personnel to qualitatively profile diverse narcotic substances and prescription drug abuses directly from urine specimens.
Because substance tracking demands absolute accuracy and split-second operational efficiency, this multiplex screening assay combines individual target antibody strips into one synchronized testing architecture. It allows rehabilitative clinics, correctional facilities, and corporate human resource compliance departments to establish definitive hiring or diagnostic pathways within minutes, eliminating the reliance on slow, costly initial laboratory gas chromatography infrastructure worldwide.
Key Performance & Technical Specifications
  • Tailored Multi-Panel Configuration: Supports fully flexible screening layouts, capturing critical targets and more simultaneously.
  • Anti-Cheating Integrity Validation: Features optional built-in chemical wells to instantly evaluate crucial specimen integrity parameters including pH, Specific Gravity, Creatinine, Glutaraldehyde, Nitrite, and Oxidants.
  • Instant Actionable Visual Readouts: Delivers highly distinct, reliable visual negative or positive color bands within 5 minutes at room temperature, ensuring optimized turnaround logistics for large-scale operations.
  • Operator-Safe Industrial presentation: Available in split-key cups, dip cards, and flat-faced multi-line cassettes to completely minimize direct operator handling or contamination risks during clinical evaluations.
B2B Sourcing, Wholesale & Custom OEM Services
As an established, globally recognized medical device factory, Hangzhou Lysun Biotechnology provides reliable high-volume international supply chains for medical wholesalers, health group distributors, and laboratory procurement groups.

Flexible OEM Solutions: We offer full private labeling services, including customized inner foil pouch print layouts, branded box packaging, and localized multilingual instructions to match your regional health ministry compliance.

Competitive Bulk Wholesale Pricing: Scalable tiered pricing matrixes are structured for container-level bulk purchasing to give your business an extreme advantage in regional IVD tenders and bulk orders.

Streamlined Regulatory Dossiers: Complete validation papers, analytical cross-reactivity studies, clinical trial metrics, cutoff parameters, and international certificates are fully accessible to accelerate cross-border customs clearance.

 

AMP rapid test device
AMP Rapid Test
China AMP Rapid Test supplier

 

Product name

AMP Rapid Test Self-Test

Item type

AMP-U11, AMP-U21

Specimens

Urine

Packing Specification

25 kits/ box

Shelf life

2 years

Test Time

Waiting about 5 minutes

Certificate

CE, ISO:13485

OEM

Acceptable

Storage condition

The kit should be stored at 2-30°C

 

REAGENTS

 

Each test consists of a reagent strip . The amount of each antigen and/or antibody coated on the strip is less than 0.001 mg for antigen conjugates and goat anti-mouse IgG antibodies, and less than 0.0015 mg for antibody components. The control zone of each test contains goat anti-mouse IgG antibody. The test zone of each test contains drug-bovine protein antigen conjugate, and the conjugate pad of each test contains monoclonal anti-drug antibody and mouse antibody-colored particle complex.

 

PRECAUTIONS

 

  • For professional in vitro diagnostic use only.
  • Do not use after expiration date indicated on the package. Do not use the test if its foil pouch is damaged. Do not reuse tests.
  • This kit contains products of animal origin. Certified knowledge of the origin and/or sanitary state of the animals does not totally guarantee the absence of transmissible pathogenic agents. It is therefore, recommended that these products be treated as potentially infectious, and handled observing the usual safety precautions (do not ingest or inhale).
  • Avoid cross-contamination of specimens by using a new specimen collection container for each specimen obtained.
  • Read the entire procedure carefully prior to performing any tests.
  • Do not eat, drink or smoke in the area where the specimens and kits are handled. Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout the procedure and follow the standard procedures for proper disposal of specimens. Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are assayed.
  • Humidity and temperature can adversely affect results.
  • The used testing materials should be discarded in accordance with local, state and/or federal regulations.

FAQ

 

Q: What is the recommended reading window for the DOA Drug Test cup?

A: Actionable visual results must be interpreted strictly at 5 minutes after specimen introduction. Do not interpret or record the line configurations after 10 minutes as it may compromise accuracy.

Q:Does the DOA Drug Test device feature built-in temperature verification?

A: Yes. Our specialized multi-panel test cups include a high-precision integrated temperature strip to instantly confirm that the freshly voided urine specimen falls within normal human physiological parameters.

Q: What is the standard minimum order quantity (MOQ) for Wholesale Multi-Drug Urine Test Panels?

A: As a premier China IVD factory, we offer flexible tiered pricing structures. For wholesale container orders, our standard packaging and bulk MOQs are highly adjustable to accommodate the logistics needs of medical distributors.

Q: Do you support custom substance combinations for OEM/ODM Drugs of Abuse Screening Kits?

A: Absolutely. We provide professional OEM/ODM services, featuring fully custom panel configurations, personalized branded boxes, and localized instruction layouts designed to satisfy your regional regulatory bodies.

Q:How does your facility ensure consistent lot-to-lot accuracy as trusted medical manufacturers and suppliers

A: We operate strictly under a certified ISO 13485 quality system. Every batch of our factory-direct rapid tests undergoes automated raw material validation and rigorous lot-to-lot screening to ensure stable international supply chain capacity and reliable accuracy.

 

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