Wholesale & OEM

Who wholesale and OEM supply is for
Wholesale and OEM supply is for distributors, importers and brand customers who order home-use diagnostic instruments and reagents in trade quantities. The company's category pages list blood glucose monitoring, hemoglobin, uric acid, cholesterol, urine analysis, fertility and pregnancy, infectious disease and drug screening products. Ask whether the specific product is available for wholesale or OEM supply.
The company's own material describes its role as designing and manufacturing home medical instruments, with its own research and development team and workshops for mould making, injection moulding, production assembly, screen and pad printing and UV curing. Those workshop descriptions are the company's own statements and are repeated here as such.
Order process as published in the company FAQ
The company FAQ sets out the order process in plain terms. Prices vary with supply and market factors, and an updated price list is issued after contact. International orders are subject to an ongoing minimum order requirement, for which no fixed figure is published on this site. Samples take about 7 days. Mass production takes 20–30 days after deposit, counting from deposit receipt and final confirmation. Payment terms listed in the FAQ are bank transfer, Western Union or PayPal, with 30% deposit and 70% against a copy of the bill of lading.
Documentation that can be provided on request includes analysis and conformity certificates, insurance and origin documents. Packaging is described in the FAQ as high-quality export packaging, with dedicated packaging for dangerous goods and validated cold-chain shipping for temperature-sensitive products; special packaging may carry an extra charge. Freight is quoted by quantity, weight and shipping method after contact. Certificates are available upon request.
What to confirm before ordering
Before payment, confirm availability, pricing, lead time, packing and documentation in writing. That confirmation step matters most for products that have no specification page on this site: only HB-101 and URA-102 carry model specifications here, and every other product's specifications must be confirmed model by model in writing.
For brand customers who want their own branding on products or packaging, the Private Label Diagnostics page describes private-label supply in general terms. For all orders, the inquiry form on the Contact page is the starting point, and the company's public contact channels are [email protected], +86 571-81957782 and +86 18868123757.
Samples as part of the order process
Samples are a normal part of the wholesale and OEM order process, not an exception to it. The FAQ's sample lead time of about 7 days means a buyer can verify a meter, a strip, a cassette or a packing configuration before committing to a trade quantity. That verification step is especially valuable where you request specifications in writing rather than relying on published specifications, because the sample lets the buyer check the confirmed specification against the physical product.
A sample order should specify the exact product and, where relevant, the model, so that the sample received is the product that will be supplied in bulk. A sample of one model does not verify another model, and a sample of one packing configuration does not verify another.
Documentation for trade orders
Documentation for a trade order typically includes the documents a buyer's market requires for import and sale, together with the product documentation that accompanies the goods. The FAQ lists analysis and conformity certificates, insurance and origin documents as available on request, and certificates are available upon request as a standing statement. Which documents apply to a specific order depends on the product and the destination market, and the document set should be confirmed in writing for the order.
For infectious disease products, documentation and market access deserve separate confirmation, because they vary by destination market and the company's own material makes market access subject to written customer confirmation. That confirmation should name the product and the market, not just the product family.