About Hubei Weikang Medical Technology Co., Ltd. - Medical Equipment & Machinery Supplier in China

China hosts Hubei Weikang Medical Technology Co., Ltd., which lists five active products across medical equipment, diagnostic kits and lighting solutions. The supplier’s catalogue is grouped under categories such as Medical Equipment & Machinery, Diagnostic Kits and Light Emitting Diode, reflecting a focus on hospital‑grade hardware and in‑vitro diagnostics. Each product is identified by its specific type, and two of the items carry HS code 3822.00, the customs classification for diagnostic or laboratory reagents. The supplier’s portfolio therefore combines both hardware (endoscope lighting, operating tables, operation lamps) and consumable test kits used for SARS‑CoV‑2 detection.

The five listed items include a Led Light Source for Endoscope, an Electric Hydraulic Operating Table and an Operation Lamp, together with a SARS‑CoV‑2 Antigen test kit and a Novel Coronavirus IgM/IgG Antibody Fast Test Kit. Both test kits are recorded with HS code 3822.00 and specify materials such as colloidal gold immunochromatographic reagent, nitrocellulose membrane and related conjugates. The hardware items are described without HS codes, but they fall within the broader HS chapters for medical devices (chapter 90). The catalogue therefore spans optical illumination components, patient‑care furniture, and rapid immuno‑assay diagnostics.

Product Range and Specialties of Hubei Weikang Medical Technology Co., Ltd.

The LED Light Source for Endoscope is a narrow‑band, high‑intensity diode typically delivering 2‑5 W output at wavelengths between 400‑460 nm, suitable for fiber‑optic illumination. In the medical lighting market, endoscope LEDs are often rated by lumen output (300‑600 lm) and power consumption, and must meet IEC 60601‑2‑46 safety standards. The Electric Hydraulic Operating Table is a motor‑driven platform with a hydraulic lift range of 300‑500 mm and a load capacity of 200‑250 kg, features commonly required for operating rooms and conforming to ISO 13485 design criteria. The Operation Lamp generally provides adjustable brightness up to 100 000 lux, with color temperature around 4 500 K, and is expected to meet IEC 60601‑2‑41 illumination standards. The SARS‑CoV‑2 Antigen test kit and the IgM/IgG Antibody Fast Test Kit are lateral flow immunoassays using colloidal gold particles; typical performance specifications include a detection limit of 10‑50 ng/mL for antigen and a sensitivity above 90 % for antibody detection, with results visible within 15‑20 minutes. These kits are packaged in sealed foil pouches to preserve reagent stability during transport.

Trade and Export Information - Hubei Weikang Medical Technology Co., Ltd.

China is a major exporter of medical devices and in‑vitro diagnostics, with the majority of shipments destined for Asia‑Pacific, Africa and Europe. Products classified under HS 3822.00 are subject to customs inspections that often require a Certificate of Analysis, a CE Declaration of Conformity and, where applicable, an ISO 13485 quality‑management certificate. Buyers typically request documentation of sterility, residual moisture content and shelf‑life for rapid test kits. Hardware such as endoscope light sources, operating tables and surgical lamps are usually shipped in 20‑ft containers on palletized wooden crates, with packaging that complies with IEC 60601‑1 safety and handling standards. Export logistics from Chinese ports frequently use FOB or CIF terms, and freight forwarders advise temperature‑controlled storage for test kits to maintain reagent integrity.

Sourcing from Hubei Weikang Medical Technology Co., Ltd. - Buyer Guidance

When sourcing the LED light source, request the product data sheet that lists wavelength, luminous flux, power consumption and IEC 60601‑2‑46 compliance. For the operating table and operation lamp, obtain the load‑capacity certificate, hydraulic pressure test report and IEC 60601‑2‑41 illumination verification. For both rapid test kits, ask for a recent batch Certificate of Analysis, validation study results (sensitivity, specificity) and proof of CE marking or equivalent regulatory clearance. Verify that the HS code 3822.00 is correctly declared on the commercial invoice and that the packaging meets ISO 11607‑1 standards for barrier integrity. Samples of each kit should be tested under the buyer’s laboratory conditions before committing to larger orders, and any deviation in material composition (e.g., colloidal gold particle size) should be clarified with the supplier.

What HS code is used for the SARS‑CoV‑2 Antigen test kit?

The catalogue records HS code 3822.00 for the SARS‑CoV‑2 Antigen test kit, which falls under the category for diagnostic or laboratory reagents.

Which material is specified for the IgM/IgG Antibody Fast Test Kit?

The kit lists colloidal gold conjugate, a nitrocellulose membrane and a sample matrix of serum, plasma or whole blood as its primary materials.

What typical performance specifications should a buyer check for the rapid test kits?

Buyers usually verify sensitivity (≥90 %), specificity (≥95 %), detection limit (10‑50 ng/mL for antigen) and result time (15‑20 minutes) as part of the product data sheet.

Are there standard certifications expected for the LED light source for endoscope?

The LED source should comply with IEC 60601‑2‑46 safety and performance standards; buyers often request the CE Declaration of Conformity or equivalent certification.

What load capacity is typical for an electric hydraulic operating table?

Operating tables in this segment commonly support 200‑250 kg and provide a hydraulic lift range of 300‑500 mm, specifications that should be confirmed with the supplier.

How are the hardware items typically packaged for export?

Hardware such as the operating table and operation lamp are usually palletized in wooden crates with protective padding, complying with IEC 60601‑1 handling requirements.

What documentation should a buyer request before placing an order for the test kits?

Buyers should request a recent Certificate of Analysis, validation study results (sensitivity, specificity), CE marking proof and, if applicable, ISO 13485 quality‑management certification.