What are the payment terms?

The accepted terms of payment are LC (Letter of Credit) and T/T (Telegraphic Transfer).

What is the lead time for production?

The lead time is 1-3 months during peak season and one month during the off-season.

Medical Luer Lock 5 Ml Disposable Syringe with Needle

Name: Medical Luer Lock 5 Ml Disposable Syringe with Needle
Brand: Ningbo Greetmed Medical Instruments Co., Ltd.
SKU: 941953725

Zhejiang, ChinaNingbo Greetmed Medical Instruments Co., Ltd.

US$0.05-0.50

5,000 Pieces

Product profile

Customization

Available

Type

Syringe

Material

Plastic

Model NO.

GT037-100 syringe

Volume

5ml

Application

Medical

Feature

Disposable

Certification

CE, ISO13485

Group

Adult

Needle

With Needle

Syringe Use

Intramuscular Injection

Size

U-40, U-100 1ml 2ml 2.5ml 3ml 5ml 50-60ml

Transport Package

Export Carton

Specification

1ml 2ml 2.5ml 3ml 5ml 50-60ml

Trademark

Greetmed

Origin

China Zhejiang

Production Capacity

10000000 Piece/Month

Key features

CE & ISO13485 Certified: Meets international medical standards with CE and ISO13485 certifications.

Customizable Sizes: Available in U-40, U-100, 1ml, 2ml, 2.5ml, 3ml, 5ml, and 50-60ml.

Medical Grade Material: Constructed from non-toxic, non-pyrogenic medical grade PP plastic.

Sterile EO Packaging: EO sterile, disposable package in PE bag/blister to prevent cross infection.

Accurate Scale Markings: High barrel clarity with accurate and clear scale markings for easy reading.

Versatile Application: Suitable for intradermal, hypodermic, intramuscular injections and blood drawing.

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.