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CE Approved Glass & Plastic Ampoule Decontamination, Liquid Injection, and Sealing Production Line
US$40,000.00-150,000.00
1 Piece
Product profile
After-sales Service
Field Installation, Commissioning and TrainingCertification
CE, GMP, ISOCondition
NewModel NO.
Customized IVEN -1Customized
CustomizedMachine Type
Liquid Filling MachineVoltage
380VWarranty
1 YearFilling Capacity
100-600bpmProcess Type
Washing, Sterilizing, Filling, Stoppering, CappingCapacity
Standard/Customized;Optional Configuration
Inspection, Labeling, Blistering, CartoningApplicable Bottle
1-30ml Glass Vial BottleFinished Dosage Form
LiquidPrecision
High PrecisionComputerized
ComputerizedTransport Package
Wooden PackageSpecification
2500*2500*1300 mm - 4280*1650*2400 mmTrademark
IVENOrigin
ChinaHS Code
8422303090Production Capacity
7000~10000 PCS/HKey features
GMP & CE Certified: Meets GMP, FDA, WHO, CE, and ISO standards for pharmaceutical production.
Full Customization: Offers full customization from samples and designs with flexible options.
High Automation Stability: Features servo control, negative pressure sealing, and low fault rates.
Efficient Washing Process: Uses 2 water/2 air outer and 3 water/4 air inner ultrasonic washing technology.
Versatile Capacity: Handles 1-20ml ampoules with capacity up to 30,000 pcs/hour.
Comprehensive Training: Includes on-site installation training and optional factory training.
Global After-Sales Support: 24-hour email/phone response and local agent dispatch within 24 hours.
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:Can you customize the machine according to our requirements?
A:
Yes.
Q:Is your equipment in accordance with GMP, FDA, WHO?
A:
Yes, we will design and manufacture the equipment according to the requirement of GMP/FDA/WHO in your country.
Q:What is your payment terms?
A:
Generally, TT or irrevocable L/C at sight.
Q:How about your after-sales service?
A:
We will reply you within 24 hours by email or phone. If we have local agent, we will arrange him to your site within 24 hours to assist you to shoot the problem.
Q:How about the staff training?
A:
Normally, we will train your staffs during the installation in your site; you are also welcome to send your staff train in our factory.
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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