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Computerized Pharmaceutical Machinery/Bio Equipment/Aerobic Fermentation Bioreactor
US$50,000.00-500,000.00
1 Piece
Product profile
Material
Wet Part Is SS316L(Alltank Body)and Other Is SS304Warranty
1 YearWorking Pressure Inside Vessel
0.25MPaModel NO.
Customized IVEN -11Working 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 CaseSpecification
customizedTrademark
IVENOrigin
ChinaProduction Capacity
CustomizedKey features
GMP Standard Compliance: Design and manufacture strictly follow GMP standards for pharmaceutical production.
Customized Configuration: Offers full customization from samples and designs with flexible options.
High Precision Control: Features intelligent PID control for pH and precise temperature management.
SS316L Wet Parts: Wet parts constructed from SS316L with SS304 for other components.
S88 & GAMP5 Compliant: Self-control program complies with S88 standard and GAMP5 guidelines.
CFR 21 Part 11 Audit Trail: Includes electronic record and signature functions meeting CFR 21 Part 11.
Versatile Cell Culture: Suitable for suspension, sheet carrier, and microcarrier culture applications.
1 Year Warranty: Provides a 1-year warranty covering core components like PLC and motor.
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: ≤1.47h 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 product comes with a 1-year warranty covering core components including PLC, engine, bearing, gearbox, motor, pressure vessel, gear, and pump.
Q:Can the bioreactor be customized?
A:
Yes, we offer full customization from samples and designs, including minor and flexible customization options.
Q:What materials are used for the bioreactor construction?
A:
The wet parts are made of SS316L (including the tank body), while other parts are constructed from SS304.
Q:Does the system comply with GMP standards?
A:
Yes, the design and manufacture strictly follow GMP standards to meet pharmaceutical production requirements.
Q:What is the working pressure capacity?
A:
The working pressure inside the vessel is 0.25MPa, and inside the jacket is 0.3MPa.
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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