25-hydroxyvitamin D (25-OH-D) Quantitative Test Cassette: Procurement Checks for Labs

25-hydroxyvitamin D (25-OH-D) Quantitative Test Cassette (Quantum Dot Fluorescence Immunochromatography)

Clinical labs handling vitamin D requests must match assay claims to the samples accepted at collection. The cassette lists whole blood, serum, and plasma as inputs, which affects phlebotomy, processing, and workflow decisions.

The supplied specification identifies it as a quantum dot fluorescence immunochromatography cassette using a competitive assay to quantitatively detect 25-OH-D. Product code GKPD052 and pack norm 25 T/box are concrete details for catalog and inventory comparison.

It is listed for professional medical, diagnostic, or laboratory workflows. The input does not provide validation data, traceability, instrument compatibility, or regulatory status, so buyers should not assume open-platform use or clearance from the label alone.

Procurement teams should verify analyzer pairing, reader requirements, sample volume, calibration, controls, storage, expiry, and documentation. Availability, configuration, MOQ, lead time, shipping, and quotation are quote-based.

Because vitamin D testing can be seasonal and high-volume, the 25 T/box format affects ordering cadence and waste. Confirm whether that pack size fits expected throughput and whether lot-level documents can be supplied.

The stated sample flexibility is useful, but the purchase decision hinges on verified performance and system fit. The product page is the practical route to confirm those details before committing.

Why it matters:
Labs should verify compatibility, regulatory status, and documentation before ordering. Request availability, pack configuration, MOQ, and a formal quotation through the product link.

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