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Endoscope Disposable Injection Needle of Sclerotherapy Needle
US$5.00-6.50
100 Pieces
Product profile
Customization
AvailableType
Surgical Supplies MaterialsMaterial
PTFEModel NO.
ATE-ZSZ-18X1800X25X6Ethylene Oxide Sterilization
Ethylene Oxide SterilizationQuality Guarantee Period
Two YearsGroup
Adult or ChildernLogo Printing
We Can Do OEM or BrandTransport Package
CartonSpecification
O. D. 2.3mm, Needle Diameter: 23GTrademark
ATEOrigin
Changzhou JiangsuHS Code
9018909010Production Capacity
500000 PCS/YearCompany profile

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableExport Year: 2014-01-01 CertifiedNearest Port: Shanghai PortAverage Response Time: ≤10.22h CertifiedTerms of Payment: LC, T/T, D/P, etc.
AI-Powered supplier vetting
SummaryJiangsu ATE Medical Technology Co., Ltd. is identified as a China-based factory established in 2013, specializing in endoscope accessories and minimally invasive diagnostic and treatment products. The supplier reports QMS compliance based on ISO 9001 and ISO 13485, 133 employees, 50 quality-control staff, five production lines, and annual disposable medical consumable productivity of 800,000 pieces. It states that sales cover APAC, the EU, and the Middle East, with after-sales service included in its business activities. The company reports ongoing product-development efforts, including valves, ligation, cytology brushes, polyp traps, ERCP, and ESD. However, the slices do not provide verified customer names or case studies, detailed customization evidence, or sufficient information to assess financial credibility. One conflicting slice lists lighter products under a different legal entity, so it should not be attributed to ATE without verification.
Supplier typeThe supplier is identified as Jiangsu ATE Medical Technology Co., Ltd., a limited company and manufacturing factory located in Changzhou, Jiangsu, China. Its stated business focuses on endoscope accessories, peripheral equipment, and minimally invasive diagnostic and treatment products.
CertificationsThe supplier states that it has established a complete quality management system based on ISO 9001 and ISO 13485. Although the management-system certification field separately says "Others," the explicit company description provides evidence of ISO-based QMS implementation.
After-Sales capabilityThe supplier describes itself as engaged in production, R&D, sales, and after-sales service for minimally invasive diagnostic and treatment products. This directly supports the existence of an after-sales service function, but no service response standards or geographic support details are provided.
R&D capabilityThe supplier reports R&D activities, innovation cooperation with partners, eight years of total R&D-engineer experience, and continued development into valves, ligation, cytology brushes, polyp traps, ERCP, and ESD. These statements provide explicit evidence of ongoing product and technology development.
Production capacityThe supplier operates as a factory with five production lines, 50 quality-control staff, a 2,588 m² manufacturing plant, 133 total employees, and stated annual productivity of 800,000 disposable medical consumable pieces. It also reports a one-month lead time in both off-peak and peak seasons, supporting a documented production capability.
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