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Quality Pediatric Infusion Set with Burette CE Certified
US$0.28-0.40
20,000 Pieces

Product profile

Type

Infusion Set

Material

Plastic

Ethylene Oxide Sterilization

Ethylene Oxide Sterilization

Model NO.

QK-B100

Quality Guarantee Period

Five Years

Group

Children

Logo Printing

Without Logo Printing

Transport Package

PE Bag and Blister Paper

Specification

64*34*38cm

Trademark

qinkai

Origin

China. Heze

HS Code

9018390000

Production Capacity

300000pieces/Every Day

Company profile

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableExport Year: 2000-07-15 CertifiedNearest Port: Qingdao PortAverage Response Time: ≤2.93h CertifiedTerms of Payment: LC, T/T, D/P, etc.

AI-Powered supplier vetting

SummaryShandong Qinkai Medical Industry Co., Ltd. is identified as a Chinese manufacturing factory established in 2017, with 212 employees and an address in Chengwu County, Shandong. The supplier reports more than 10 production lines, substantial stated capacities for needles, syringes, infusion sets, and burette infusion devices, and export markets covering South America, Southeast Asia/Mideast, and Europe. It cites CE, ISO 13485, and ISO 9001:2008 certifications, supported by 50 quality-control staff and 10 R&D engineers. Evidence confirms manufacturing scale, export activity, and named overseas trade records, but does not establish after-sales procedures, customization services, audited financial strength, or detailed customer performance outcomes.
Supplier typeThe supplier is explicitly described as a factory/manufacturer and a limited company in China, operating in the medical and health sector. Its Chengwu County address is located in a Medical Equipment Industrial Park, supporting the classification as a medical-device manufacturing supplier.
CertificationsThe supplier explicitly states that it holds CE, ISO 13485, and ISO 9001:2008 certifications and describes a quality management system, testing instruments, and quality-control practices. The records do not provide certificate numbers, issuing bodies, or validity dates, but they do provide direct evidence of certification claims.
R&D capabilityThe supplier reports 10 R&D engineers, strong technical capabilities, advanced production equipment, automatic production lines, and ongoing product improvement. These statements support an internal technical and development capability, although no specific patents, new-product examples, or R&D achievements are provided.
Production capacityThe supplier is identified as a factory with more than 10 production lines, a 35,600 m² manufacturing plant, over 23,000 m² of purification workshop area, and stated annual capacities of 600 million needles, 600 million syringes, 300 million infusion sets, and 15 million burette infusion devices. It also reports lead times of within 15 working days in off-peak periods and one month in peak periods, providing strong direct evidence of production scale and delivery capability.
Client casesTrade records identify BAKPHARM LIMITED and AHMAD ZIA NIAZI LTD as buyers, with products including burette infusion sets and disposable syringes shipped to or associated with Kenya, Pakistan, and Afghanistan. These records demonstrate at least two named buyer relationships and relevant product transactions, but they do not provide customer testimonials, repeat-order evidence, delivery performance, or project outcomes.

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