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Urology Surgical Device Double Pigtail Ureteral Stent
US$0.01
1 Piece
Product profile
Customization
AvailableType
Ureteral StentMaterial
Medical High Polymer MaterialEthylene Oxide Sterilization
Ethylene Oxide SterilizationQuality Guarantee Period
Two YearsGroup
Adults and ChildrenLogo Printing
with Logo or Without LogoColor
White or GreenLength
15cm, 18cm, 26cm, 28cm etc..Transport Package
Plastic Package and Carton PackageSpecification
F4, F4.8, F5, F6, F7, F8Trademark
RebornOrigin
ChinaHS Code
9018390000Production Capacity
50000 Pieces/YearCompany profile
Business Type: Manufacturer/FactoryExport Year: 2016-06-01Nearest Port: GuangzhouAverage Response Time: ≤11.54hTerms of Payment: T/T, Western UnionInternational Commercial Terms(Incoterms): EXW
AI-Powered supplier vetting
SummaryThe supplier is identified as a Chinese manufacturer/factory operating in the health and medicine sector, with a stated production site in Zhuzhou, Hunan. It reports more than 10 production lines, 11–20 quality-control staff, and 21–30 years of combined R&D-engineer experience. ISO 13485 and GMP management-system certifications are stated, and OEM service is available. The product range focuses on urological and endourological devices, including ureteral access sheaths, stone baskets, guidewires, PCNL sets, and balloon dilatation catheters. The supplier states that it has self-operated import/export rights and began exporting in 2016, although exports account for only 21%–30% of total sales. Evidence of after-sales support, detailed innovation performance, audited financial strength, and a broad customer portfolio is limited. One trade record and one associated Ukrainian buyer are reported.
Supplier typeThe supplier is explicitly classified as a manufacturer/factory and as a limited company in China. Its associated industry is manufacturing, and the stated company name is Hunan Reborn Medical Science and Technology Development Co., Ltd., with another record identifying Hunan Ruibang Medical Technology Development Co., Ltd.
CertificationsThe supplier explicitly reports ISO 13485 and GMP certification of its management systems. These certifications are directly relevant to medical-device quality and manufacturing controls, although the slices do not provide certificate numbers, validity dates, or certification scopes.
R&D capabilityThe supplier reports 21–30 years of total R&D-engineer experience and lists multiple urological device products, including new products. These details support an established technical-development function, but no patents, R&D investment, product-launch record, or independently verified innovation outcomes are provided.
Production capacityThe supplier is identified as a factory with a stated physical production location, more than 10 production lines, and 11–20 quality-control staff. These explicit operational indicators support substantial production capability, while actual capacity utilization and product-specific output are not disclosed.
Customization capabilityThe supplier explicitly states that OEM service is available, providing direct evidence of customization support. The slices do not specify customization scope, minimum order requirements, tooling capability, development timelines, or examples of completed customized products.
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