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IV Flow Regulator
US$0.01-0.60
100,000 Pieces

Product profile

Customization

Available

Type

Infusion Set

Material

Plastic

Application

Medical

Feature

Disposable

Certification

CE, ISO13485

Group

Adult

Needle

Without Needle

Syringe Use

Medical

Delivery Days

20 Days

Quality Guarantee

5 Yeas

Ethylene Oxide

Ethylene Oxide Sterilization

Transport Package

Blister or PE Packing

Specification

CE ISO

Trademark

JN MEDICAL

Origin

China

HS Code

90183900

Production Capacity

100000000/Year

Key features

CE and ISO13485 Certified: Meets international medical standards with CE and ISO13485 certifications for safety and quality.
Customizable Components: Options for air vented spike, needle, Y injection port, and Luer lock or slip connectors.
ETO Sterilization: Sterilized using Ethylene Oxide with a protective cap that allows gas entry but prevents bacteria.
High-Quality Materials: Made from soft, kink-resistant medical grade PVC, polyethylene, and polystyrene components.
Comprehensive Accessories: Includes vented spike, drip chamber, fluid filter, flow regulator, and latex tube.
OEM and ODM Support: Manufacturer offers both OEM and ODM services with 15 R&D engineers for custom solutions.
Fast Delivery and Warranty: 20-day delivery time and a 5-year quality guarantee for peace of mind.
Established Manufacturer: Factory established in 2001 with 120 employees and a 12,700 sqm plant area.

Company profile

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableExport Year: 2003-11-08 CertifiedNearest Port: Shanghai PortAverage Response Time: ≤9.38h CertifiedTerms of Payment: LC, T/T, D/P, etc.

AI-Powered supplier vetting

SummaryAnhui JN Medical Device Co., Ltd. is a China-based limited company in Anhui, established in 2001 according to the company profile, with 120 employees and a 12,700 m² manufacturing plant. It focuses on disposable medical devices, including syringes, infusion sets, needles, and related products. Reported production capabilities include more than 10 production lines and annual output of 500 million disposable syringes. The supplier reports 15 years of R&D engineer experience, 11–20 quality-control staff, one-month lead times in both peak and off-peak seasons, and exports representing 51%–70% of sales. It claims exports to more than 100 countries and lists Africa, East Asia, and Europe as primary markets. However, certification details are recorded only as “Others,” and the available evidence does not establish after-sales procedures, customization capability, or comprehensive customer references. Trade records show transactions involving buyers in Uzbekistan and Tanzania, but the available records are limited.
Supplier typeThe supplier is identified as a limited company operating in the health and medicine sector, with disposable syringes as a product keyword and a broader portfolio of disposable infusion sets, needles, and related medical devices. Its profile states that it was established in 2001, while another company description states that JN MEDICAL was founded in 1995, creating an inconsistency in the reported founding date.
R&D capabilityThe supplier reports 15 years of R&D engineer experience and claims to operate advanced automatic production lines for syringes, needles, and infusion sets. These statements support technical and engineering capability, but the slices do not provide verifiable information on patents, new product development, or specific innovation outcomes.
Production capacityProduction evidence is substantial: the supplier reports a 12,700 m² plant, more than 10 production lines, 500 million disposable syringes of annual output, a GMP-standard clean workshop described as 12,000 m², and one-month lead times in both peak and off-peak periods. The profile also states that it exports its products to more than 100 countries and regions.
Client casesThe supplier claims that its products are exported to more than 100 countries and regions, and the trade records identify buyers in Uzbekistan and Tanzania, including ZUMA PHARMA МЧЖ and DOSSA PHARMACEUTICALS LIMITED. These records provide some customer and market evidence, but the available transaction sample is small and does not establish a broad, independently verified customer portfolio.

Product Q&A

Q:What certifications does the IV Flow Regulator have?
A:
The product holds CE and ISO13485 certifications, ensuring compliance with international medical device standards.
Q:Can I customize the IV Flow Regulator components?
A:
Yes, options are available for air vented spikes, needles, Y injection ports, and Luer lock or slip connectors.
Q:How is the product sterilized?
A:
The product is sterilized using Ethylene Oxide (ETO), protected by a cap that prevents bacterial entry while allowing gas penetration.
Q:What materials are used in the construction?
A:
It is made from soft, kink-resistant medical grade PVC, polyethylene, and polystyrene, adhering to ISO standards.
Q:Does the manufacturer offer OEM or ODM services?
A:
Yes, the manufacturer provides both OEM and ODM services supported by a team of 15 R&D engineers.

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