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Pharmaceutical & Medical Fluid Bed Granulator with ISO CE Certifcate
US$50,000.00-250,000.00
1 Piece

Product profile

Certification

CE, GMP, ISO, CE

Production Capacity (Kg/Batch)

15/30--300/500

Dimension(L*W*H)

1.5*1.3*5m--3.5*3.5*10m

Vessel Volume(L)

45-1530

Fan Power(Kw)

7.5-75

Electric Heating Power(Kw)

30-120

Steam Consumption(Kg/H)

180-677

Weight of Mian Machine(Kg)

800-3500

Finished Dosage Form

Granules

Precision

High Precision

Voltage

380V

Computerized

Computerized

Customized

Customized

Condition

New

Warranty

1 Year

After-sales Service

Field Installation, Commissioning and Training

Transport Package

Standard Export Package

Specification

3.2 x2.5 x2.5M

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

Multi-Function Granulation: Combines top spray granulating and bottom spray pellet coating in one machine.
Wide Capacity Range: Production capacity spans from 5 to 500 kg per batch across multiple models.
Comprehensive Certifications: Equipped with CE, GMP, and ISO certifications for pharmaceutical compliance.
Full Customization Options: Offers full, minor, and flexible customization from samples or designs.
High Precision Output: Designed for high precision granulation suitable for solid dosage forms.
One-Year Warranty: Includes a 1-year warranty covering mechanical defects and parts.
Global After-Sales Support: Provides field installation, commissioning, and training services.
Versatile Application: Ideal for pharmaceutical, chemical, and food industries for aqueous products.

Company profile

Shanghai Iven Pharmatech Engineering Co., Ltd.
Years of Export ExperienceLow MOQPatents AwardedProduct Certification
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: ≤1.73h 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 range?
A:
The production capacity ranges from 5 kg/batch to 500 kg/batch depending on the model selected.
Q:Is the machine customizable?
A:
Yes, we offer full, minor, and flexible customization options based on samples or designs.
Q:What certifications does the equipment hold?
A:
The machine holds CE, GMP, and ISO certifications ensuring compliance with international standards.
Q:What is the warranty period?
A:
We provide a 1-year warranty for the machine.
Q:Do you provide after-sales service?
A:
Yes, we offer field installation, commissioning, and training services globally.

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