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Superior Quality ABS Lateral Flow Rapid Plastic Test Kit Empty Cassette
US$0.05-0.20
10,000 Pieces
Sample price:US$0.50/piece.Request sample
Product profile
Customization
AvailableType
IVD ReagentShelf Life
Two YearsModel NO.
DLM-5.5Format
Cassette/MidstreamColor
White/Red/Blue/CustomizedTransport Package
Plastic Bag, Sealed CartonSpecification
5.5mmTrademark
OEM/ NeutralOrigin
ChinaHS Code
3923300000Production Capacity
300000 PCS/MonthCompany profile

Business Type: Manufacturer/Factory, Trading Company CertifiedNearest Port: Shanghai Port, Beijing PortAverage Response Time: ≤3.52h CertifiedTerms of Payment: LC, T/T, D/P, etc. CertifiedInternational Commercial Terms(Incoterms): FOB, CIF, CFR
AI-Powered supplier vetting
SummaryHebei Times Medical Technology Co., Ltd. is identified as a China-based manufacturer/factory engaged in medical devices and in vitro diagnostic reagents, including urine test strips, infectious disease tests, uncut sheets, and related raw materials. The supplier reports ISO 9001 certification, 21–30 years of combined R&D engineer experience, 50 quality-control staff, and five production lines. It states that it has 14 years of industry experience, a mature supply chain, and partners in more than 50 countries, with customer deployments across multiple regions. However, the available trade records show only one transaction per listed period and a single associated buyer in Vietnam, so the breadth of independently evidenced customer cases and trading history remains limited. Evidence is insufficient to assess financial credibility, customization capability, or after-sales service in detail.
Supplier typeThe supplier is explicitly identified as Hebei Times Medical Technology Co., Ltd., a manufacturer/factory based in Hebei, China. Its stated business focuses on the research, development, and sales of medical devices and in vitro diagnostic reagents.
CertificationsThe supplier reports holding ISO 9001 certification. This provides explicit evidence of a certified quality-management system, although no additional certifications are stated.
R&D capabilityThe company states that it conducts research and development in medical devices and in vitro diagnostic reagents, and reports 21–30 years of total R&D engineer experience. Its product scope includes diagnostic tests and home-diagnosis products, supporting an R&D presence, but no specific patents, new-product results, or documented innovation achievements are provided.
Production capacityThe supplier is classified as a manufacturer/factory and reports five production lines, 50 quality-control staff, a mature supply chain, and quality control covering semi-finished products, plastic parts, accessories, and production equipment. These stated resources support production capability, although actual capacity utilization and delivery performance are not documented.
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