CE/ISO Approved Endoscopic Disposable Grasping Forceps Polypectomy Snare for Gi Endoscopy in Various Shapes Customized Acceptable with CE Marked ISO 13485

Name: CE/ISO Approved Endoscopic Disposable Grasping Forceps Polypectomy Snare for Gi Endoscopy in Various Shapes Customized Acceptable with CE Marked ISO 13485
Brand: Zhejiang Soudon Medical Technology Co., Ltd.
SKU: 2074169575

Zhejiang, ChinaZhejiang Soudon Medical Technology Co., Ltd.

US$5.99-10.99

100 Pieces

Sample price:US$10.99/piece.Request sample

Product profile

Customization

Available

Sterilization

Feature

Disposable

Model NO.

SD-03-M230-35T

Application

Clinical

Material

Plastic

Certification

CE, FDA, ISO13485

Power Type

Electric

Group

Adult

Sheath O.D.

2.3mm

Working Length

2300mm

Loop Width

35mm

Shape

Shield Type

Transport Package

Bag+Inner Box

Specification

160mm*104mm for individual product packaging

Trademark

With logo or without logo

Origin

China, Zhejiang Province

HS Code

9018903090

Production Capacity

1000000PCS/Year

Company profile

National Award receivedFast DeliveryFull CustomizationManagement Certification

Zhejiang Soudon Medical Technology Co., Ltd.

Zhejiang, 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: 4 Years CertifiedNearest Port: Shanghai Port, Ningbo PortAverage Response Time: ≤8.22h

AI-Powered supplier vetting

SummaryThe supplier is a combined company engaged in medical-device-related production and sales, including licensed Class II and Class III medical-device activities. It demonstrates broad customization and ODM capability, reports new-product development within the past year, and has OEM experience with well-known brands. Service procedures for corrective actions, complaints, supplier assessment, and finished-product inspection are documented and followed. However, the supplier reports no quality assurance in its quality-control processes, has only two quality-control inspectors, and lacks in-stock capacity, overseas warehouses, overseas agents or branches, and overseas service coverage. Manufacturing capacity is also weakened by the absence of a valid contract with affiliated subcontractors. Financial credibility cannot be assessed from the provided information.

Supplier typeThe supplier is identified as a combined company. Its stated business scope includes production and operation of Class II and Class III medical devices, as well as hygiene products and disposable medical supplies subject to required approvals.

After-Sales capabilityThe supplier has documented and followed procedures for corrective and preventive actions and customer complaints, and it has written procedures and records for supplier-service assessment. However, it reports no in-stock capacity, overseas warehouse, overseas showroom, overseas agent or branch, and zero countries with overseas services, limiting demonstrated international after-sales coverage.

R&D capabilityThe supplier reports new products within the past year, offers ODM services and broad design support, and holds one national science and technology progress award. Its stated emphasis on innovation is consistent with these capabilities, although it has no available SDK.

Production capacityProduction-related evidence includes assembly-line and precision-workshop facilities, two quality inspectors, standardized finished-product inspection instructions, and OEM service for well-known brands. Deficiencies include no stated quality assurance in quality-control processes, no in-stock capacity, and no valid contract with affiliated subcontractors; the business scope nevertheless includes licensed medical-device production activities.

Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, minor customization, flexible customization, and full customization. The same broad design-service range is reported in both R&D and facility-related information, providing clear evidence of extensive customization capability.

Client casesThe supplier reports OEM service for well-known brands and participation in the CMEF offline trade show. These are identifiable customer or market-exposure indicators, but no customer names, project descriptions, order volumes, or verifiable case details are provided.