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Good Performance IV Bag Turnkey Solution Plant Non-PVC Soft Bag IV Infusion Manufacturing Machine Plant EPC Pharma Construction
US$300,000.00-1,200,000.00
1 Piece
Product profile
Packaging Material
PVCWarranty
1 YearFinished Dosage Form
LiquidPrecision
High PrecisionCertification
CE, GMP, ISOVoltage
380VComputerized
ComputerizedCustomized
CustomizedCondition
NewTransport Package
Cartons; Wooden Case;Specification
3.2 x2.5 x2.5MProduction Capacity
2 PCS/YearKey features
100% Film Utilization: Special 130mm design ensures no waste edges, saving 10mm film per bag compared to competitors.
Quick Size Changeover: Switch between IV bag sizes (100ml-5000ml) in just 0.5-1 hour, enhancing production flexibility.
Low Leakage Rate: Reliable heating and welding systems ensure IV bag leakage rates remain below 0.03%.
Turnkey EPC Solution: Integrated engineering includes clean rooms, water treatment, filling, and validation per EU GMP/FDA.
High Precision Control: Single HMI and control system manage the entire line, ensuring stable operation and easy maintenance.
Patent Safety Design: Patented contact filling nozzles prevent solution overflow and particle generation during production.
Space Saving Structure: Compact design reduces machine length by 1/3, significantly saving room space and running costs.
Automated Quality Control: Auto detection and faulty rejection systems automatically remove unqualified bags after cap welding.
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: ≤2.46h 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 warranty period for the IV bag manufacturing plant?
A:
The standard warranty period is 1 year.
Q:What is the production capacity of the IV bag machine?
A:
Production capacity ranges from 900 bph to 8000 bph depending on the model (Srd1a to Srd12a) and bag size (500 ml).
Q:Can the machine produce different IV bag sizes?
A:
Yes, the machine supports IV bag sizes ranging from 100ml to 5000ml with a quick changeover time of 0.5-1 hour.
Q:What certifications does the equipment hold?
A:
The equipment is certified with CE, GMP, and ISO, and the turnkey solution complies with EU GMP, US FDA cGMP, PICS, and WHO GMP.
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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