Import Coronavirus Antibody Tests — Buy in Bulk from Supplier in United States

Kore20 LLC offers three rapid serology kits: the SGTi‑flex COVID‑19 IgM/IgG kit containing 25 tests per unit, the STANDARD Q COVID‑19 IgM/IgG Duo kit with 40 tests per unit, and the Anti‑SARS‑CoV‑2 Rapid Test supplying 50 tests per unit. Each test detects and differentiates IgM and IgG antibodies against SARS‑CoV‑2, delivering a visual result within ten to fifteen minutes without the need for additional laboratory equipment. The kits are CE‑IVD marked, FDA‑cleared, ISO 13485 certified and produced in a Korea GMP‑certified facility, providing a recognised regulatory framework for international trade.

Typical usage of these kits involves a 10 µl sample of whole blood, plasma or serum applied to the cassette, after which the specimen migrates by capillary action. The reagents remain stable when stored at 2‑8 °C, and manufacturers usually assign a shelf life of twelve months from the date of manufacture. The test format is designed for point‑of‑care settings, making it suitable for clinics, emergency departments and remote health‑outreach programmes where rapid serological screening is required.

Importers should confirm that the buyer holds the necessary regulatory approvals for in‑country distribution of CE‑IVD or FDA‑cleared devices and verify the exact lot numbers before shipment. While the listing does not disclose minimum order quantities, each kit is supplied as a sealed unit ready for immediate use. Trade terms such as Incoterms, payment method and lead time must be agreed directly with Kore20 LLC, as they are not specified in the product data.

Kore20 LLC is listed as an imported‑tier supplier with a harbour‑level trust rating, and the marketplace data shows a zero percent response rate, indicating that contact may need to be initiated through alternative channels. The company is based in the United States, but no further address details are provided in the available profile.

The supplier focuses on distributing diagnostic test kits that meet international regulatory standards such as CE‑IVD, FDA clearance and ISO 13485. No additional corporate history, employee count or client portfolio is disclosed, and the listing does not specify any certifications beyond those already attached to the products.