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CE Approved Automatic Pharmaceutical Machines Supplier Ampoule Filling Machine Manufacturers
US$30,000.00-120,000.00
1 Piece
Product profile
Automation Grade
AutomaticWarranty
1 YearFilling Capacity
100-600bpmModel NO.
Customized IVEN -11Process Type
Washing, Sterilizing, Filling, Stoppering, CappingCapacity
Standard/Customized;Optional Configuration
Inspection, Labeling, Blistering, CartoningApplicable Bottle
1-30ml Glass Vial BottleFinished Dosage Form
LiquidPrecision
High PrecisionCertification
CE, GMP, ISOVoltage
380VComputerized
ComputerizedCustomized
CustomizedCondition
NewAfter-sales Service
Field Installation, Commissioning and TrainingTransport Package
Wooden PackageSpecification
2500*2500*1300 mm - 4280*1650*2400 mmTrademark
IVENOrigin
ChinaHS Code
8422303090Production Capacity
7000~10000 PCS/HKey features
GMP & CE Certified: Equipment meets GMP, FDA, WHO standards with CE and ISO certifications.
Compact Continuous Line: Integrates washing, sterilizing, filling, and sealing in a single linkage.
Universal Bottle Compatibility: Suitable for 1-20ml ampoules and vials with convenient part changing.
Customized Configuration: Offers optional inspection, labeling, blistering, and cartoning modules.
Low Maintenance Design: Features wear-proof manipulators and hinge-type heat structures.
Efficient Cleaning System: Combines ultrasonic, cross-pressure jet, and ultra-filtration technologies.
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: ≤1.57h 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:Can the machine be customized according to requirements?
A:
Yes, we offer full customization, minor customization, and flexible customization based on samples or designs.
Q:What certifications does the equipment have?
A:
The equipment is certified with CE and ISO, and can be designed to meet GMP, FDA, and WHO standards.
Q:What are the payment terms?
A:
Generally, we accept TT or irrevocable L/C at sight, as well as LC, D/P, PayPal, and Western Union.
Q:What is the after-sales service policy?
A:
We reply within 24 hours via email or phone, arrange local agents within 24 hours if available, and provide engineer dispatch for 6-12 months.
Q:How long does a turnkey project take?
A:
A turnkey project typically takes about 1 year from layout design to installation and commissioning.
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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