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Latest Advanced International Technology Dry Powder Granulator/Dry Powder Granulation Machine
US$40,000.00-180,000.00
1 Piece
Product profile
Certification
CE, GMP, ISOFeature
High Working EfficiencyRaw Material
304/316ssKey Selling Points
Easy to Operate;Long Service LifeRoller and Feed Speed Regulation Type
Electromagnetic Speed/Variable Frequency Speed ConVideo Outgoing-Inspection
ProvidedRoll Size(mm)
CustomizedRoll Speed(Rpm)
CustomizedCore Components
PLC, Motor, Pressure VesselRoller Pressure
20MPaType
Preparation MachineryFinished Dosage Form
GranulesPrecision
High PrecisionVoltage
380VComputerized
ComputerizedCustomized
CustomizedCondition
NewWarranty
1 YearAfter-sales Service
Field Installation, Commissioning and TrainingTransport Package
Standard Export PackageSpecification
3.2 x2.5 x2.5MTrademark
IVENOrigin
ChinaProduction Capacity
CustomizedKey features
High Working Efficiency: Integrates extrusion, crushing, and granulating functions for continuous processing.
Customizable Roll Size and Speed: Roll size and speed are fully customized to meet specific production needs.
GMP Compliant Design: Complies with GMP requirements with modular design and easy-to-clean structure.
No Drying Required: Dry granulation process eliminates the need for drying, preserving active ingredients.
Improved Flowability and Solubility: Enhances powder flowability and drug solubility for better manufacturing efficiency.
Low Dust and Waste: Generates less dust and waste compared to wet granulation, ensuring environmental safety.
1-Year Warranty: Provides a 1-year warranty with field installation, commissioning, and training support.
High Precision Control: Features PLC control with electromagnetic or variable frequency speed regulation.
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: ≤2.04h 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 industries can use this dry powder granulator?
A:
It is widely used in pharmaceutical, food, and chemical industries for granulating materials that are wet, hot, easily broken, or agglomerated.
Q:Is the roll size and speed customizable?
A:
Yes, both the roll size (mm) and roll speed (Rpm) are fully customizable to suit your specific requirements.
Q:What is the warranty period and after-sales service?
A:
We provide a 1-year warranty. After-sales service includes field installation, commissioning, and training.
Q:Does the machine require drying after granulation?
A:
No, the dry granulation process does not require water or other liquids, so no drying is needed, which helps preserve active ingredients.
Q:What certifications does the machine have?
A:
The machine 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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