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Urethral Stent CE ISO Certification
Negotiable
500 Sets

Product profile

Customization

Available

Type

Catheter

Material

Plastic

Model NO.

5F 6F 7F

Ethylene Oxide Sterilization

Ethylene Oxide Sterilization

Quality Guarantee Period

Two Years

Group

Adult

Logo Printing

With Logo Printing

Size

6fr-26fr

balloon

5-15ml/5-30ml

Lumen

One/Two/Three

Length

40cm

Transport Package

Carton

Specification

silicon

Trademark

ABLE

Origin

China

HS Code

9018390000

Key features

CE & FDA Certified: Product holds CE and FDA marks ensuring compliance with international safety standards.
Customizable Specifications: Sizes range from 6fr-26fr, balloon volumes 5-15ml/5-30ml, and lengths up to 40cm.
Two-Year Warranty: Comprehensive quality guarantee period of two years for all ureteral stents.
Ethylene Oxide Sterilized: Sterilized using Ethylene Oxide method for safe single-use application.
Versatile Clinical Use: Ideal for retrograde pyelography, drainage, kidney stone pain relief, and post-surgery healing.
Custom Logo Printing: Supports custom logo printing services for branding purposes.

Company profile

Guangdong Baihe Medical Technology Co., Ltd.
High Repeat Buyers ChoiceYears of Export Experience
Business Type: Manufacturer/FactoryExport Year: 2001-10-01Nearest Port: huangpu, shenzhen, shanghaiAverage Response Time: ≤5.28hTerms of Payment: LC, T/T, PayPal, etc.International Commercial Terms(Incoterms): FOB, EXW, CIF, Others

AI-Powered supplier vetting

SummaryThe supplier demonstrates broad medical-device manufacturing and sales scope, including multiple device classes, protective equipment, catheters, dialyzers, blood lines, and related products. It offers OEM, ODM, flexible customization, and customization from designs or samples, and reports new product development within the past year. Production-related strengths include valid contracts with associated subcontractors, in-stock capability, one-month average lead times in both peak and off-season, and 100 quality assurance and quality control inspectors. Service management procedures, complaint-handling procedures, and corrective and preventive action procedures are documented and followed. The supplier also supports overseas agents or branches, training services, and has participated in an offline trade show. However, it has no overseas warehouse or showroom, no available SDK, and the provided information does not establish formal certifications, detailed customer cases, or sufficient evidence to assess...
Supplier typeThe supplier is positioned as a medical-device manufacturer and seller, with stated capabilities covering Class I, II, and III medical-device production or management, protective equipment, masks, and sanitary or single-use medical supplies. This indicates a broad, regulated healthcare-product business scope rather than a general trading-only profile.
After-Sales capabilityThe supplier has written procedures and implementation records for customer complaint handling, corrective and preventive actions, and broader service-capability assessment. It also provides overseas-agent or branch support and training in Hong Kong, Singapore, Turkey, India, and Pakistan, although no overseas warehouse or showroom is available.
R&D capabilityThe supplier reports new products within the past year, offers ODM services and multiple design-development options, and uses ERP, OA, CRM, and SAP systems for digitalized operational management. However, it has no available SDK, so software-development integration capability is specifically limited.
Production capacityThe supplier reports valid manufacturing contracts with every associated subcontractor, in-stock capability, one-month average lead times in both peak and off-season, and 100 quality assurance and quality control inspectors. Its stated product and facility information includes catheters, dialyzers, blood lines, and an ethylene oxide sterilizer production facility, supporting a substantial manufacturing operation.
Customization capabilityThe supplier explicitly provides flexible, minor, and full customization, including customization from customer designs and samples. It also offers ODM services, indicating capability beyond standard catalog supply.

Product Q&A

Q:What certifications does the urethral stent have?
A:
The product is CE and FDA certified, ensuring it meets rigorous international quality and safety standards.
Q:What are the available customization options?
A:
Customization is available for size (6fr-26fr), balloon volume (5-15ml/5-30ml), lumen (One/Two/Three), and length (up to 40cm).
Q:What is the warranty period for this product?
A:
We provide a two-year quality guarantee period for our ureteral stents.
Q:How is the product sterilized?
A:
The stents are sterilized using the Ethylene Oxide method to ensure they are safe for single use.
Q:What is the average lead time for orders?
A:
The average lead time is one month, regardless of whether it is peak season or off-season.

Send Inquiry

*To:Guangdong Baihe Medical Technology Co., Ltd.Guangdong Baihe Medical Technology Co., Ltd.
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