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PE/PP IV Fluids Technology Machine Plastic Bottle Sterile Packaging Bfs System
US$50,000.00
1 Piece
Product profile
After-sales Service
Field Installation, Commissioning and TrainingWarranty
1 YearType
Volumetric Filling MachineModel NO.
customizedAutomatic Grade
AutomaticMaterial Type
GranularFilling Valve Head
Multi-HeadFeed Cylinder Structure
Multi-Room FeedingDosing Device
Capacity CupFilling Principle
PressurePackaging Container Lifting Structure
Pneumatic LiftingStructure
RotaryPackaging
BoxPackaging Material
PlasticDeflasher
Internal PunchingPower Source
3p/AC380VInstalled Power
42kwMachine Structure
Dark Side White Side UnseperationPacking Materials
PE/PPCapacity (Bottle Per Hour)
The Capacity Is 3000 PCS/Hour(1ml); The Capacity IFilling Accuracy
1.5% (Based on 5ml) with PurifieManufacturing Standard
cGMPTransport Package
Stardard PackingSpecification
customizedTrademark
IVENOrigin
ChinaKey features
cGMP Compliant Design: Design, MOC, and assembly meet new GMP standards for pharmaceutical production.
High Production Capacity: Capacity ranges from 1000 to 18000 bottles per hour, customizable to needs.
Advanced BFS Technology: Blow-Fill-Seal process in sterile filtered air-shower for primary packaging.
Energy Efficient Structure: Compact integrated design reduces clean workshop area and energy consumption.
Servo Motor Extrusion: Low-speed long-screw extruder reduces thermal stress and controls preform size.
Flexible Customization: Customizable capacity, bottle specs (0.2ml-1000ml), and minor design adjustments.
Comprehensive After-Sales: Includes field installation, commissioning, training, and 1-year warranty.
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: ≤2.50h 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 the BFS machine?
A:
The capacity ranges from 1000 to 18000 bottles per hour (BPH), which can be customized according to user requirements.
Q:What materials are used for the plastic bottles?
A:
The machine uses polypropylene (PP), high-density polyethylene (HDPE), or low-density polyethylene (PE) for primary packaging.
Q:Does the machine meet GMP standards?
A:
Yes, the design, material of construction, manufacture, assembly, and debugging meet the requirements of the new GMP standards.
Q:What is the warranty period for this equipment?
A:
We provide a 1-year warranty for the machine.
Q:What after-sales services are provided?
A:
We offer field installation, commissioning, and training services for the equipment.
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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