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GMP Certified Seamless IV Infusion Set Production Line
US$150,000.00-420,000.00
1 Piece
Product profile
After-sales Service
Field Installation, Commissioning and TrainingAutomation
AutomationCondition
NewModel NO.
customizedProduction Continuity
ContinuousProduction Scope
Product LineCapacity
5000 Sets/Hour for Infusion Set Assembly SpeedQualified Product Rate
98%Power Supply
380 V, 50 Hz, 22 KwAir Consumption
1-5 M3/MinFunction
MultifunctionalKey Words
Infusion Set Production Line Turnkey SolutionApplication
Disposable Infusion Set Factory;PharmaceuticalProduct Specification
Infusion Set/ IV SetInfusion Set Design
CustomizedMaterial
Stainless SteelProduction Speed
60-70PCS/Min;Customized;Automatic Production Line
ComprehensiveFlexible Production
Intelligent ManufacturingRhythm
Flow Production LineTransport Package
Standard Export PackageSpecification
3000*1200 *2000 mmTrademark
IVENOrigin
ShanghaiProduction Capacity
CustomizedKey features
High Production Capacity: Achieves 5000 sets/hour assembly speed with a qualified product rate of 98%.
GMP and FDA Compliant: Designed for GMP, FDA, and WHO workshop standards ensuring safety and quality.
Flexible Module Design: Modular structure allows flexible production of different kinds of IV infusion sets.
Low Power Consumption: Automated feeding and assembly ensure stable running with low energy usage.
Easy Maintenance: Cleanable design and simple maintenance requirements for efficient operation.
Minimal Labor Requirement: Only 2-3 workers needed to supervise all production stations.
Customizable Production: Offers customized infusion set design and production speed options.
Comprehensive Automation: Full automatic production line with intelligent manufacturing and flow rhythm.
Company profile
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: ≤2.00h 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.
Product Q&A
Q:What is the production capacity of this line?
A:
The production capacity is 5000 sets per hour for infusion set assembly speed.
Q:What is the qualified product rate?
A:
The qualified product rate is guaranteed to be at least 98%.
Q:Does this equipment meet GMP standards?
A:
Yes, the production line is suitable for GMP, FDA, and WHO workshop standards.
Q:How many workers are needed to operate the line?
A:
Only 2-3 workers are required to supervise all stations.
Q:What is the power supply requirement?
A:
The power supply requirement is 380 V, 50 Hz, 22 Kw.
Send Inquiry
*To:
Shanghai Iven Pharmatech Engineering Co., Ltd.
Shanghai Iven Pharmatech Engineering Co., Ltd.*Content:
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