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Automated Aseptic IV Drip Bag Manufacturing and Filling Line with GMP
US$200,000.00-400,000.00
1 Piece
Product profile
Application
Machinery & Hardware, Medical&Pharmaceutical;Warranty
Field Maintenance and Online Video SupportFeature
Durable, Quick Changeover;Model NO.
Customized IVEN -1Filling Volume
20--1000mlCapacity
CustomizedFinished Dosage Form
LiquidPrecision
High PrecisionCertification
CE, GMP, ISOVoltage
380VComputerized
ComputerizedCustomized
CustomizedCondition
NewAfter-sales Service
Field Installation, Commissioning and TrainingTransport Package
Wooden Case, CartonsSpecification
3.26x2.0 x2.1MTrademark
IVENOrigin
ChinaProduction Capacity
20 PCS/YearKey features
One-Stop Automated Production: Automatically completes film feeding, printing, bag making, filling, and sealing in a single machine.
High Precision Filling System: Uses E+H mass flowmeter and high-pressure system for accurate filling with zero qualified bag errors.
Flexible Customization Options: Supports customized capacity, filling volume (20-1000ml), and various port designs like single/double hard ports.
Intelligent PLC Control: Features multi-language touch screen, servo motor drive, and automatic alarm/fault display for precise control.
Efficient Quick Changeover: Switch between different bag specs (100/250/500/1000ml) easily by changing only the mould and printing panel.
GMP & CE Certified: Meets strict GMP standards for aseptic IV drip bag manufacturing with CE certification for safety.
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: ≤2.27h 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 types of IV bags can this machine produce?
A:
It produces Non-PVC soft bags for general solutions, dialysis, parenteral nutrition, antibiotics, and disinfectants, with capacities ranging from 50 to 5000ml.
Q:Is the filling volume customizable?
A:
Yes, the filling volume is customizable, typically ranging from 20ml to 1000ml, and can be adjusted via the man-machine interface.
Q:How does the machine handle different bag designs?
A:
It supports various designs including single boat type ports, single/double hard ports, and double soft tube ports, allowing one line to make two different types.
Q:What certifications does the equipment have?
A:
The equipment is certified with CE, GMP, and ISO standards, ensuring compliance with pharmaceutical manufacturing requirements.
Q:What is the minimum order quantity (MOQ)?
A:
The minimum order quantity is 1 Set.
Send Inquiry
*To:
Shanghai Iven Pharmatech Engineering Co., Ltd.
Shanghai Iven Pharmatech Engineering Co., Ltd.*Content:
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