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RO + EDI Water Purification Plant GMP Pharmaceutical Purified Water System
US$80,000.00
1 Piece
Product profile
Customization
AvailableApplication
Biotechnology Industry, Food & Beverage Factory, Food Safety, Forensic Science, Pharmaceutical IndustryCapacity
500 L/hrModel NO.
5000L/HCertification
CE, FDA, GMP, ISOControl System
Fully AutomaticTreatment Process
Electrodeionization, Filtration, Reverse Osmosis, SofteningWarranty of core components
One YearWelding Method
Sanitary Welding / Orbital Welding (Optional)Sealing Material
FDA Approved EPDM / PTFEDistribution Loop
316L Ss PipingHuman-Machine Interface
Touch Screen HMIToc
Complies with USP / Ep RequirementsWater Temperature
5 - 30 ℃Product Contact Material
Stainless Steel 316LNon-Contact Parts
Stainless Steel 304Purified Water Tank
316L Stainless SteelTransport Package
WoodenSpecification
otherTrademark
WEMACOrigin
ChinaHS Code
8421219990Production Capacity
One Piece / MonthKey features
GMP Compliant Design: Meets GMP, cGMP, USP, EP, and ChP standards for pharmaceutical purified water.
Customized Capacity: Production capacity adjustable from 500 to 30,000 L/h based on specific needs.
Advanced RO + EDI System: Double-pass RO combined with EDI for stable quality without chemical regeneration.
Siemens PLC Control: Features Siemens PLC with HMI for automatic operation, monitoring, and alarms.
Microbial Control Options: Includes UV, ozone, or hot-water sanitization to prevent biofilm and contamination.
Customized Pretreatment: Tailored pretreatment including filtration, softening, and chemical dosing.
Company profile
Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤2.74h
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 a pharmaceutical purified water system?
A:
It is an integrated water purification system designed to produce high-quality purified water for pharmaceutical manufacturing, typically using pretreatment, RO and EDI technologies.
Q:What is the production capacity of the system?
A:
The system can be customized from 500 L/h to 30,000 L/h according to your production requirements.
Q:Why is RO combined with EDI?
A:
RO removes most dissolved salts, organic matter and contaminants, while EDI provides continuous deep deionization to achieve stable purified-water quality without routine chemical regeneration.
Q:What kind of raw water can be used?
A:
Normally, qualified municipal drinking water is used as the feed water. The pretreatment system is customized according to the local raw-water analysis.
Q:Is the system fully automatic?
A:
Yes. The system can be equipped with Siemens PLC + HMI for automatic operation, monitoring, alarms and process control.
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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