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IV Fluid/Lvp/IV Infusion/IV Solution/Normal Saline Plant /Turnkey Project/ Factory
US$300,000.00-1,200,000.00
1 Piece
Product profile
Warranty
1 YearCapacity
100ml, 250ml, 500ml.1000mlWeight
3-12tPower
32kwFunction
Filling EquipmentKey Selling Points
AutomaticWeight (Kg)
3500 KgApplicable Industries
Manufacturing Plant, PharmaProduct Capacity
5800~6500 Bags/ HourBag-Making Film
Non-PVC FilmBag-Making Form
Single Port, Heat Insulation SealOverall Size
3.26X2.0 X2.1m--8.97X4.65 X2.25mPackaging
Wooden CaseFinished Dosage Form
LiquidPrecision
High PrecisionCertification
CE, GMP, ISOVoltage
380VComputerized
ComputerizedCustomized
CustomizedCondition
NewAfter-sales Service
Field Installation, Commissioning and TrainingTransport Package
Cartons; Wooden Case;Specification
3.2 x2.5 x2.5MTrademark
IVENOrigin
ChinaProduction Capacity
2 PCS/YearKey features
100% Film Utilization: Special 130mm width design ensures no waste edges between bags, saving material and energy.
Quick Size Changeover: Switch between IV bag sizes in just 0.5-1 hour, enhancing production flexibility.
Low Leakage Rate: Reliable heating and welding system ensures leakage rate is less than 0.03%.
Compact Structure: Reduces machine length by 1/3, saving room space and operational running costs.
Patent Contact Filling: Safe filling nozzle prevents solution overflow and particle generation during filling.
Auto Fault Rejection: Automatic detection system rejects unqualified bags after cap welding for quality assurance.
Turnkey Project Solution: Integrated engineering solution including clean room, water treatment, and filling systems.
GMP Compliant Design: Complies with EU GMP, US FDA cGMP, PICS, and WHO GMP standards for pharmaceutical 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: ≤2.25h 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 equipment?
A:
We provide a 1-year warranty for all our equipment.
Q:What is the production capacity of the IV bag machine?
A:
The production capacity ranges from 900 to 8000 bags per hour, depending on the model and bag size (e.g., 500ml).
Q:Can the machine size be customized?
A:
Yes, the machine supports full customization, including capacity, weight, power, and overall dimensions to fit specific factory layouts.
Q:What is the minimum order quantity (MOQ)?
A:
The minimum order quantity is 1 set.
Q:What certifications does the equipment hold?
A:
The equipment is certified with CE, GMP, and ISO standards.
Send Inquiry
*To:
Shanghai Iven Pharmatech Engineering Co., Ltd.
Shanghai Iven Pharmatech Engineering Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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