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Industrial Deionized System RO System Pure Water System
US$35,000.00-65,000.00
1 Set
Product specifications
MOLPW-3000
Product profile
Customization
AvailableApplication
Biotechnology Industry, Chemical industry, Clinical Diagnosis, Energy & Mining, Food & Beverage Factory, Food Safety, Forensic Science, Pharmaceutical IndustryCapacity
1000lphCertification
CE, FDA, GMP, ISOControl System
Fully AutomaticTreatment Process
Chlorination, Electrodeionization, Reverse Osmosis, Softening, UV DisinfectionWarranty of core components
1 YearDisinfection
Heat DisinfectionDocuments
Iq,Oq,Pq,Dq, Fat, Sop, etcMaterial
SS304+SS316LPump Brand
Cnp or AppointedRO Brand
DuPont, Ge or OtherUser Manual
English Version or OtherTransport Package
Wooden BoxSpecification
1900*1600*2100Trademark
MolecularOrigin
ChinaHS Code
8421219990Production Capacity
500set/YearKey features
Advanced RO+EDI Technology: Integrates Reverse Osmosis and Electrodeionization to produce ultra-pure water exceeding pharmacopoeia standards.
Modular Sanitary Design: Pharmaceutical-grade stainless steel construction with dead-leg-free piping to prevent microbial growth.
Intelligent Automation: PLC+HMI control system with real-time monitoring and automatic/manual operation modes for efficiency.
Energy-Efficient Operation: Smart optimization reduces energy consumption by up to 30% and lowers operational costs via EDI.
Multi-Layer Safety Protection: Comprehensive alarms, self-diagnosis, and pressure relief ensure continuous safe operation and contamination prevention.
Turn-Key Solution: Complete service from technical design and production to shipping, installation, and training.
High Recovery Rate: Concentrated water recycling design increases total system recovery rate for resource efficiency.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 10 Years CertifiedNearest Port: Shanghai Port; Chongqing PortAverage Response Time: ≤0.41h
AI-Powered supplier vetting
SummaryThe supplier is identified as a manufacturing factory in Chongqing, China, offering direct drinking water, industrial pure water, pharmaceutical pure water, medical central pure water, and ultra-pure water equipment. It provides end-to-end services from demand analysis and design through installation, commissioning, training, and after-sales support. The supplier demonstrates broad customization and ODM capabilities, reports new products within the past year, and has an available SDK. Quality and supplier-service procedures are documented and followed. It has inventory capability, overseas agents or branches, export experience, and has served customers domestically and internationally. However, the provided information confirms no valid manufacturing-capacity contract with related subcontractors, no overseas warehouse, no overseas showroom, and no stated national science and technology progress award. Certification holdings and detailed financial credibility cannot be determined from the provided data.
Supplier typeThe supplier is explicitly identified as a factory, with its location in Jiulongpo District, Chongqing, and its associated companies classified in manufacturing. The company is also described as a combined company rather than an offshore entity.
After-Sales capabilityThe supplier states that it provides installation, debugging, training, and after-sales service as part of its full-process offering. It also reports overseas agents or branches and overseas service coverage in Pakistan, supporting service reach beyond its domestic base.
R&D capabilityThe supplier reports that it had new products within the past year, provides ODM services, and has an available SDK. These details provide explicit evidence of product-development and technical-support capability, although the record of national science and technology progress awards is zero.
Production capacityThe supplier is a manufacturing factory with a stated scope covering water-treatment equipment and certain disinfection, medical-mask, and related production activities. It reports in-stock capability, but there is no valid contract between the factory and related subcontractors, and no overseas warehouse capability, creating a documented weakness in manufacturing-capacity governance and international fulfillment infrastructure.
Customization capabilityBoth design-capability records list customization from samples, customization from designs, full customization, minor customization, and flexible customization. The supplier also explicitly reports ODM availability, indicating a broad range of customization and original-design support.
Client casesThe supplier states that it has served over 20,000 domestic and international customers and provides OEM services for well-known brands. It also reports participation in ASIA PHARMA EXPO 2023 and overseas service coverage in Pakistan, but no named customer cases are provided.
Product Q&A
Q:What is the typical process flow of a pharmaceutical purified water system?
A:
A typical PW system usually includes pretreatment (multimedia filtration, activated carbon, softener), reverse osmosis (RO), electrodeionization (EDI), storage, and distribution loop with constant circulation and UV / ozone sanitization.
Q:Why is EDI commonly used instead of mixed bed ion exchange in modern PW systems?
A:
EDI avoids chemical regeneration, reduces chemical contamination risk, ensures stable water quality, and is more compliant with GMP requirements for continuous and reliable production.
Q:What key quality parameters must be monitored for purified water in pharmaceuticals?
A:
Key parameters include conductivity, TOC, microbiological count, endotoxins (if for WFI preparation), pH, hardness, and heavy metals, in accordance with pharmacopeial standards such as USP, EP, or ChP.
Q:What is the difference between Purified Water (PW) and Water for Injection (WFI)?
A:
PW is produced by RO/EDI and used for non-parenteral products. WFI has stricter limits for endotoxins and microbes, usually produced by distillation or multiple-effect evaporation from purified water.
Q:How to control microbial growth in the purified water distribution loop?
A:
Maintain continuous circulation at a certain flow rate, control loop temperature (hot water sanitization), regularly sanitize with heat or chemical agents, install UV sterilizers, and avoid dead legs.
Send Inquiry
*To:
Molewater System Co., Ltd.
Molewater System Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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