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DOA Rapid Urine Test Device Strip/Cassette/Panel (Colloidal Gold )
A urine drug-of-abuse test is a consumable within a broader screening workflow, not a standalone conclusion. The listed scope is specific: five analyte classes, one sample type, and several pack sizes.
Professional drug screening depends on consumables that match existing bench routines, sample handling, and documentation practice. Guoke Medical lists the DOA Rapid Urine Test Device as a lateral flow chromatographic immunoassay for the qualitative detection of amphetamines, benzodiazepines, cocaine, morphine and tetrahydrocannabinol in urine.
The specification gives product code GKPD043 and pack norms of 1, 10, 20, 25, 40 or 50 tests per box. The text describes a cassette; the title also names strip and panel formats, so the exact configuration should be confirmed before ordering.
Intended use is qualitative detection, so a result reflects an assay threshold rather than a measured drug concentration. Confirmatory procedures and reporting rules remain part of the laboratory’s own protocol.
Pricing, minimum order quantity, lead time, shelf life, storage conditions and shipping are not stated. Buyers should request instructions for use, certificate of analysis, and current regulatory or registration documents during quotation.
Because each box covers five analyte classes, continuity of supply matters more than a single-unit price comparison. Lot-to-lot performance, replacement availability, and pack counts aligned with testing volume are practical checks.
The narrow, verifiable specification is the useful part: a defined sample type, analyte set, product code and pack range. Everything beyond that belongs in written confirmation.
Why it matters:
Buyers should treat format, documentation and supply continuity as the decisive checks, because the published specification alone does not establish clinical suitability or procurement terms.
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