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Customized Capacity Bioreactor / Pharmaceutical Fermentor /Industrial Bioreactor
US$50,000.00-500,000.00
1 Piece
Product profile
Application
Pharmaceutical Industry, Healthcare IndustryMaterial
Wet Part Is SS316L(Alltank Body)and Other Is SS304Warranty
1 YearModel NO.
Customized IVEN -11Working Pressure Inside Vessel
0.25MPaWorking Pressure Inside Jacket
0.3MPaPLC
Self-Developing PLC/Siemens PLCBasic Functions
Culture Microorganism, Adjust pH, Do, Temp.AntifoaOptional Functions
Weigh, Pressflow, Discharged Gas Detect, Multi-FeeCapacity
50L-500LType
Preparation MachineryFinished Dosage Form
LiquidPrecision
High PrecisionCertification
CE, GMP, ISOVoltage
380VComputerized
ComputerizedCustomized
CustomizedCondition
NewAfter-Sales Service
Field Installation, Commissioning and TrainingTransport Package
Wooden CaseTrademark
IVENOrigin
ChinaProduction Capacity
CustomizedKey features
GMP & ASME Compliance: Design and manufacture strictly follow GMP regulations and ASME-BPE requirements.
Wide Capacity Range: Available volumes range from 5 liters to 30 kiloliters for various production scales.
High Precision Control: Equipped with self-developing PLC or Siemens PLC for precise pH, DO, and temperature control.
Multi-Function Design: Features replaceable mixing paddles and optional functions like weighing and gas detection.
Versatile Application: Suitable for monoclonal antibodies, vaccines, and recombinant protein fermentation.
Quality Assurance: 100% inspection for finished products including visual and function checks.
Professional Support: Provides field installation, commissioning, and training services globally.
Flexible Customization: Offers full customization from samples, designs, or minor adjustments to meet specific needs.
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: ≤1.49h 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 warranty period for the bioreactor?
A:
The warranty period is 1 year for the machine and core components including PLC, engine, bearing, and pressure vessel.
Q:What certifications does the bioreactor have?
A:
The bioreactor is certified with CE, GMP, and ISO standards, ensuring compliance with international quality and safety regulations.
Q:What is the minimum order quantity (MOQ)?
A:
The minimum order quantity is 1 set, allowing for flexible purchasing options for laboratories and pilot plants.
Q:What is the lead time for production?
A:
The average lead time is 1-3 months, with peak season times potentially extending up to one month depending on demand.
Q:What payment terms are accepted?
A:
We accept LC, T/T, D/P, PayPal, Western Union, and small-amount payments for your convenience.
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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