What is the minimum order quantity?

The minimum order quantity is 1 set.

What is the average lead time for delivery?

The average lead time is 1-3 months, depending on the season.

Does the machine include automatic quality detection?

Yes, it features automatic online detection for burrs, angles, glue amount, and needle blockage.

OEM ISO Approved IV Catherter Making Equipment High Efficient Intravenous Needle Manufacturing Machine

Name: OEM ISO Approved IV Catherter Making Equipment High Efficient Intravenous Needle Manufacturing Machine
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2066986855

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-300,000.00

1 Piece

Product profile

Injection Site

Intravenous

Material

FEP or TPU

Warranty

1 Year

Model NO.

customized IVEN

Product Type

Pen Type, Butterfly Type, Y Type

Size

Customized;8g, 20g, 22g, 24G, 14G, 16g, 18g

Packing

Blister

Properties

Injection & Puncture Instrument

Feature

Safety

OEM

Welcome

Advantage

Puncture Safely & Quickly

Properity

Less Pain

Color

Orange, Grey, Green, Pink, Blue, Yellow, Purple

Precision

High Precision

Certification

CE, GMP, ISO

Voltage

380V

Computerized

Customized

Condition

New

Finished Dosage Form

IV Catherter

After-sales Service

Field Installation, Commissioning and Training

Transport Package

Wooden Case

Specification

6500*4300*3500 mm

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

High Production Capacity: Efficient manufacturing with a production capacity of 2,000 pcs/hour.

Advanced Quality Control: Automatic online detection of burrs, angles, glue amount, and needle blockage.

Flexible Customization: Customized product types, sizes, and packing options to meet specific needs.

Safety & Precision: High precision servo system ensures safe puncture and avoids needle waste.

Complete Turnkey Solution: Offers full pharmaceutical plant solutions from design to installation and training.

ISO & CE Certified: Equipment meets international standards with CE, GMP, and ISO certifications.

Reduced Contamination Risk: Vertical silicification and gas blowing greatly reduce residual silicone oil.

Professional After-Sales: Includes field installation, commissioning, and training for seamless operation.

Company profile

Years of Export ExperienceLow MOQPatents AwardedProduct Certification

Shanghai Iven Pharmatech Engineering Co., Ltd.

Shanghai, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 19 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤2.28h CertifiedTerms of Payment: LC, T/T, D/P, etc.

AI-Powered supplier vetting

SummaryThe supplier is a combined company offering pharmaceutical and medical production equipment, including vial, ampoule, prefilled syringe, oral liquid, tablet, capsule, visual inspection, packaging, and logistics solutions. It provides extensive customization and integrated services such as process design, equipment selection, installation, commissioning, and validation. Export activity is substantial, with 71%–90% of sales from exports and 19 years of export experience. Quality assurance, ISO9001:2015 certification, CE capability, manufacturing contracts, and finished-product inspection instructions are documented strengths. However, the supplier lacks in-stock, overseas warehouse, overseas showroom, overseas agent or branch capabilities, and has no written procedures for service assessment, corrective actions, or complaint handling. R&D evidence is limited: no SDK, no new products in the past year, and no ODM or major-brand OEM services. No specific customer cases are provided.

CertificationsThe supplier reports an ISO9001:2015 certificate and CE certification capability, providing explicit evidence of quality-management and product-compliance credentials. However, the slices do not specify the scope, validity period, or products covered by these credentials.

After-Sales capabilityThe supplier lists installation, commissioning, validation, maintenance, debugging, repair, training, and integrated consulting services, and provides equipment installation-related offerings. Nevertheless, it has no overseas agents or branches, no overseas warehouse or showroom, and no written procedures or records for complaint handling, service assessment, or corrective and preventive actions, indicating an operational weakness in documented after-sales management.

R&D capabilityThe supplier has customization-oriented R&D services, but reports no available SDK, no new products during the past year, no ODM service, and no OEM service for popular brands. These explicit limitations indicate weak evidence of current product innovation and platform development.

Production capacityThe supplier covers multiple pharmaceutical equipment production lines, including vial and ampoule, prefilled syringe and cartridge, oral liquid, tablet and capsule, inspection, packaging, and logistics systems. It has valid manufacturing contracts with each affiliated subcontractor, follows finished-product inspection instructions uniformly, and reports quality assurance, although no quantitative production-capacity data is provided.

Customization capabilityThe supplier explicitly offers customization from samples, designs, full customization, minor customization, and flexible customization. Its integrated solution includes process design, conceptual and construction design, equipment selection, model customization, installation, commissioning, and validation, demonstrating broad customization coverage.