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Advanced Reverse Osmosis EDI Systems for Pharmaceutical Water Treatment
US$30,000.00
1 Piece
Product profile
Customization
AvailableApplication
Biotechnology Industry, Energy & Mining, Food & Beverage Factory, Pharmaceutical IndustryCapacity
1000 L/hrModel NO.
100L/HCertification
CE, FDA, GMPControl System
Fully AutomaticTreatment Process
Chlorination, Electrodeionization, Filtration, Reverse Osmosis, Softening, UV DisinfectionWarranty of core components
One YearPretreatment
Multi-Media Filter, Activated Carbon FilterPrimary Purification
Dual-Stage Reverse Osmosis (RO)Polishing Technology
Electrodeionization (EDI)Output Conductivity
≤ 1.3 Us/CmOutput Toc
< 500 PpbWelding Standard
Automatic Orbital Welding (Internal Passivation)Transport Package
Wooden CaseSpecification
otherTrademark
WEMACOrigin
ChinaHS Code
8419409090Production Capacity
One Piece / MonthKey features
Dual RO & EDI Technology: Integrates dual-stage Reverse Osmosis and Electrodeionization for ultra-pure water without chemical regeneration.
High Capacity Output: Produces 1000 liters per hour with adjustable settings to meet specific requirements.
Pharmaceutical Grade Materials: Constructed with SS316L stainless steel and sanitary fittings meeting hygiene standards.
cGMP Compliance: Validated design with complete documentation support including DQ/IQ/OQ/PQ.
Fully Automatic Control: PLC-based system with touchscreen HMI, data logging, and real-time monitoring.
Energy & Water Efficient: Advanced recovery design significantly lowers water waste and energy usage.
Customizable Solutions: Scalable and modular design allows capacity increase and WFI integration.
Company profile
Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤3.40h
AI-Powered supplier vetting
SummaryThe supplier is identified as a trading company with a broad technical, equipment, software, and engineering-related business scope. It demonstrates professional technical R&D positioning, 3D software design, ODM, OEM, and multiple customization options. Quality and service procedures are partly established, including inspection instructions, complaint handling, supplier assessment, and corrective-action records. However, the supplier has only one quality inspector, has exported for one year, lacks raw-material traceability labels and written quality records, and has no overseas warehouse or showroom. Innovation evidence is mixed because no new products were reported in the past year and no SDK is available. Financial information is present only as year references, without sufficient evidence to assess credibility.
Supplier typeThe supplier is explicitly classified as a Trading Company. Its stated scope covers technical services, technology development, equipment sales, software development, IoT services, industrial engineering design, and equipment repair, indicating a technically oriented trading and service business rather than a clearly documented manufacturer.
After-Sales capabilityThe supplier has documented and followed procedures for complaint handling, supplier service-capability assessment, and corrective/preventive actions, and it reports in-stock service capability. However, it lacks overseas warehouse and showroom capabilities, so the evidence supports structured service handling but not comprehensive overseas support.
R&D capabilityThe supplier reports professional technical R&D capability, 3D software design, ODM services, and OEM services for popular brands. Counterbalancing this, it reported no new products during the past year and has no available SDK, so the evidence supports design and development services but not strong recent product innovation.
Customization capabilityThe supplier explicitly provides customization from samples, full customization, and customization from customer designs. It also offers 3D software design and ODM services, providing clear evidence of broad customization capability.
Product Q&A
Q:What is the production capacity of the system?
A:
The system is capable of producing 1000 liters per hour, with adjustable settings to meet specific requirements.
Q:Does the system meet pharmaceutical water standards?
A:
Yes, the output water quality meets USP/EP/ChP standards for Purified Water (PW) and Water for Injection (WFI) pretreatment.
Q:What materials are used for the wetted parts?
A:
The system is constructed with SS316L or high-grade stainless steel, ensuring all wetted parts meet pharmaceutical hygiene standards.
Q:Is the system fully automatic?
A:
Yes, it features a PLC-based control system with an intuitive touchscreen HMI for fully automatic operation and real-time monitoring.
Q:Can the system capacity be customized?
A:
Yes, the system offers scalable and modular customization for increased capacity or integration with WFI or pure steam generators.
Send Inquiry
*To:
Shandong Eagle Pharma Machinery Co., Ltd.
Shandong Eagle Pharma Machinery Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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