Disposable Double J Ureteral Stent with Pusher Guidewire ISO Certification

Name: Disposable Double J Ureteral Stent with Pusher Guidewire ISO Certification
Brand: Suzhou Ruizhuoyuan Medical Sci & Tech Co., Ltd.
SKU: 2258549715

Jiangsu, ChinaSuzhou Ruizhuoyuan Medical Sci & Tech Co., Ltd.

US$7.00

1-99 Sets

US$6.80

100-999 Sets

US$6.60

1,000-1,999 Sets

US$6.40

2,000+ Sets

Product specifications

Ureteral Stent

Set Package

Guide Wire

Product profile

Type

Surgical Supplies Materials

Material

Ethylene Oxide Sterilization

Model NO.

US-01-01-****/JS

Quality Guarantee Period

Three Years

Group

Children & Adults

Logo Printing

With Logo Printing

Product Name

Disposable Ureteral Stent

Keywords

Ureteral Stent

Sterilization

EOS

Length

100mm-300mm

Specifications

F3, F4, F4.5, F4.8,F5, F6, F7, F8

Combination Package

Ureteral Stent, Guidewire, Boosting Tube

Certification

ISO13485

Instrument Classification

Class II

Sample

Sample to Supply

Term of Validity

3 Years

Usage

Minimally Invasive Surgical Materials

Packing

Plastic Package

Stock

Yes

Transport Package

Plastic Package and Carton

Specification

US-01-01-0314/JS

Trademark

RUIBITONG

Origin

Jiangsu, China

HS Code

9018390000

Company profile

Suzhou Ruizhuoyuan Medical Sci & Tech Co., Ltd.Jiangsu, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 2 Years CertifiedNearest Port: Zhangjiagagn PortAverage Response Time: ≤2.41h

AI-Powered supplier vetting

SummaryThe supplier is described as a manufacturer integrating R&D, production, sales, and service for disposable sterile medical equipment and instruments. It reports broad customization, 3D design, ODM, and OEM capabilities, supported by AutoCAD, Pro/E, and SolidWorks, four years of combined R&D engineer experience, and available R&D design documentation. Quality processes include three inspectors, documented finished-product inspection instructions, quality assurance, and recorded corrective, preventive, and complaint-handling procedures. Production evidence is limited to one production line, while valid contracts with associated subcontractors and inventory capacity are reported. No supplier-management-system certification, overseas warehouse, or overseas showroom is reported. Export experience is two years, with exports representing 1%–10% of sales and primary markets listed as domestic. Customer cases are not specifically documented.

Supplier typeThe supplier identifies itself as a manufacturer integrating R&D, production, sales, and service for disposable sterile medical equipment and instruments. Its stated business scope also includes precision machinery, hardware, and plastics, indicating a manufacturing-oriented profile rather than a purely trading role.

CertificationsThe supplier-management-system certification field is explicitly recorded as “NIL.” This is direct evidence that no such certification is reported in the provided information.

After-Sales capabilityThe supplier has documented procedures and records for corrective and preventive actions and for handling customer complaints, supporting a defined service-response process. However, no separate evidence describes warranty execution, technical support after delivery, or overseas service infrastructure; the supplier also reports no overseas warehouse or showroom.

R&D capabilityThe supplier reports new products during the past year, 3D software design, ODM services, and four years of total R&D engineer experience. Its engineers use AutoCAD, Pro/E, and SolidWorks, and design-input, output, review, verification, and validation documents are available for audit; no SDK is available.

Production capacityThe supplier describes complete production facilities and operates one production line, with molding and coating facilities, three quality inspectors, standardized finished-product inspection instructions, and inventory capacity. Valid contracts with associated subcontractors are also reported, but the available information does not quantify output capacity or establish large-scale production capability.

Customization capabilityBoth R&D and design-service records list customization from samples, designs, full customization, minor customization, and flexible customization. The supplier also reports 3D design, ODM services, and engineering support using multiple CAD tools, providing explicit evidence of broad customization capability.