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Influenza type A and B（Flu A/B）Ag Rapid Test Cassette(Colloidal Gold)
Rapid influenza testing depends on specimen type, pack configuration, and professional-use documentation. Those are the practical details buyers must confirm before ordering.
The product is identified as a Guoke Medical item under code GKPD027, within a Testing for Respiratory Diseases portfolio. Its stated format is an immunochromatographic assay using colloidal gold for qualitative detection of influenza A and B nucleoprotein antigen. It is recommended for professional use only.
The supplied indications cover nasopharyngeal, oropharyngeal, and nasal swab specimens. Influenza A detection includes the H1N1 subtype, while the assay also targets influenza B. These specimen and target details determine whether the cassette fits an existing clinical or laboratory workflow.
Listed pack sizes are 1, 10, 20, 25, 40, and 50 tests per box. That range can accommodate different procurement scales, but availability by configuration must be checked. The source does not confirm which sizes are stocked at any given time.
The test is described as an aid in differential diagnosis of influenza A and B infection. It is not presented as a standalone diagnostic conclusion. Professional interpretation remains part of its stated use.
Buyers should verify current pack configuration, compatible collection supplies, instructions, documentation, minimum order quantity, lead time, shipping, and quotation. The ordering section routes those requests through Scientific China.
The input does not specify sensitivity, specificity, shelf life, storage conditions, regulatory approvals, or kit components. Those gaps need direct confirmation before purchase. Procurement should not infer them from the product title alone.
Why it matters:
Specimen type, pack size, and professional-use labeling shape both workflow fit and purchasing risk. Confirm those variables before committing to a diagnostic order.
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