Digital Fertility Testing System Sits Between Device and Consumable Procurement

Digital Fertility Testing System

The Digital Fertility Testing System is listed as a Guoke Medical product in the Testing for Pregnancy portfolio. Its stated use is quantitative or semi-quantitative detection of hormone in human urine, placing it in professional medical, diagnostic, or laboratory workflows.

The system comprises the Digital Fertility Tracker and Test Midstreams. That split matters operationally: one part is the tracker, while the other is the test midstreams supplied in boxes of 1, 10, 20, 25, 40, or 50 tests under product code GKPD047.

Biomarker is given simply as urine. The listing does not name the specific hormone, assay range, sensitivity, result format, or clinical decision thresholds. Buyers should treat those as items to confirm in the technical dossier rather than assume from the product category.

The available pack sizes range from single-test boxes to 50-test boxes. That spread affects inventory planning and per-test cost comparisons, especially where laboratory or clinic demand is uneven.

Compatibility between tracker and test midstreams is another verification point. The listing mentions compatible options but does not specify them, so configuration should be confirmed with the supplier before purchase.

Documentation, minimum order quantity, lead time, shipping, and formal quotation are handled by inquiry. For procurement, these commercial terms may matter as much as the stated test format.

Why it matters:
The system combines a tracker and test midstreams, so buyers should verify the exact hormone, pack configuration, compatibility, and documentation before committing to a supply plan.

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