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Is the product sterilized?

Yes, the product is sterilized and intended for single use.

High Quality Giving Set Medical Disposable IV Infusion Set for Single Use

Name: High Quality Giving Set Medical Disposable IV Infusion Set for Single Use
Brand: Ningbo Greetmed Medical Instruments Co., Ltd.
SKU: 2016472615

Zhejiang, ChinaNingbo Greetmed Medical Instruments Co., Ltd.

US$0.02-0.05

10,000 Pieces

Sample price:US$1.00/piece.Request sample

Product profile

Customization

Available

Sterilization

Feature

Disposable

Model NO.

GT034-100 infusion set

Application

Clinical

Material

Plastic

Certification

CE, ISO13485

MOQ

10000PCS

Tube

PVC

Item No.

Gt034-105

IV Regulator

Transport Package

1PC/PE Bag

Trademark

Greetmed

Origin

China

Production Capacity

100000PCS/Month

Key features

Sterile Single-Use Design: Sterilized IV infusion set designed for single use only, ensuring safety and hygiene.

Air-Vent Technology: Equipped with air-vent for direct and smooth transfusion of I.V. fluids into veins.

CE and ISO13485 Certified: Meets international safety standards with CE and ISO13485 certifications.

PVC Tube Material: Constructed with high-quality PVC tubing for durability and flexibility.

PP IV Regulator: Features a polypropylene (PP) regulator for precise flow control.

Fast Fluid Replacement: Enables rapid infusion of medication or fluid replacement from sterile bags.

Global Market Reach: Exporting to North America, Europe, Asia, Africa, and Oceania since 2003.

Flexible Payment Terms: Accepts LC and T/T payment methods for international trade convenience.

Company profile

Ningbo Greetmed Medical Instruments Co., Ltd.

Zhejiang, China

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2003-06-06Nearest Port: shanghaiAverage Response Time: ≤18hTerms of Payment: LC, T/TInternational Commercial Terms(Incoterms): FOB, CIF

AI-Powered supplier vetting

SummaryGREETMED demonstrates OEM and ODM capability, broad customization options, recent new-product activity, and stated quality-control procedures with material traceability. It reports ERP-based process digitization, CE certification capability, participation in MEDICA 2025, and procedures for corrective actions and complaint handling. However, it has no overseas showroom, agent, or branch, reports zero countries with overseas services, lacks an SDK, and has no fixed-source pollution registration or factory environmental impact assessment report. Supplier-assessment procedures are documented but lack records, and the stated peak-season lead-time information is inconsistent, limiting confidence in operational evaluation.

Supplier typeThe supplier is identified through the GREETMED own-brand reference and reports both OEM services for well-known brands and ODM services. Its offerings therefore support classification as a manufacturer with own-brand, OEM, and ODM capabilities, although the slices do not provide a formal legal or industry classification.

CertificationsThe supplier reports CE certification capability, which is explicit evidence of holding or supporting this product certification. No broader certification portfolio is provided, so the assessment is limited to CE.

After-Sales capabilityThe supplier has documented corrective and preventive action and customer-complaint procedures with follow-up records, and describes professional after-sales support. However, it has no overseas showroom, agent, or branch and reports zero countries with overseas services; service assessment procedures exist without records, indicating strong stated internal handling but limited overseas coverage and verification.

R&D capabilityThe supplier reports new products during the past year, ODM capability, and enterprise digitalization through ERP, with additional digital-development indicators recorded. It does not have an available SDK, but that limitation does not negate the demonstrated product-development and process-digitization evidence.

Production capacityProduction capability is supported by stated advanced equipment, standardized operations, quality-assurance processes, material traceability, written work instructions, and uniformly followed inspections. The supplier also reports 30 qualified suppliers, but its service-capability assessment procedure has no records and the peak-season lead-time entry is internally inconsistent, so operational verification remains incomplete.

Customization capabilityThe supplier explicitly offers customization from samples and designs, full and minor customization, flexible customization, and ODM services. This is direct evidence of broad customization capability.

Client casesThe supplier reports OEM service for well-known brands and participation in the offline MEDICA 2025 trade show. These are evidence of brand-serving experience and market exposure, but no named customer cases or project details are provided.