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Sofe Tapered Tip Hydrophilic Ureteral Stent

Name: Sofe Tapered Tip Hydrophilic Ureteral Stent
Brand: Hunan Reborn Medical Science and Technology Development Co., Ltd.
SKU: 911151235

Hunan, ChinaHunan Reborn Medical Science and Technology Development Co., Ltd.

Negotiable

1 Piece

Product profile

Customization

Available

Type

Surgical Supplies Materials

Material

Model NO.

reborn-UST

Ethylene Oxide Sterilization

Quality Guarantee Period

Two Years

Group

Adult

Color

White or Green, Blue

Length

15cm, 18cm, 26cm, 28cm etc..

End

Two Ends Open or One End Close

Retrival Tether

with or Without

Transport Package

Plastic Package and Carton Package

Specification

F4, F4.8, F5, F6, F7, F8

Trademark

Reborn

Origin

China

HS Code

9018390000

Production Capacity

50000 Pieces/Year

Key features

Hydrophilic Coating: Enables smooth and atraumatic advancement for improved patient comfort.

Customizable Options: Color, length, end type, and retrieval tether can be customized per clinical needs.

Temperature Control: Becomes soft after placement inside the body for better biocompatibility.

High Biocompatibility: Designed to provide patients with a better experience and reduced irritation.

Certified Sterilization: Strict Ethylene Oxide sterilization with ISO and CE certification.

2-Year Warranty: Comprehensive quality guarantee period for two years.

OEM/ODM Support: Global cooperation available for OEM and ODM customization services.

Company profile

Hunan Reborn Medical Science and Technology Development Co., Ltd.

Hunan, China

Business Type: Manufacturer/FactoryExport Year: 2016-06-01Nearest Port: GuangzhouAverage Response Time: ≤15hTerms 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.