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SHANGHAI CHONGYANG WATER TREATMENT EQUIPMENT CO.,LTD
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Membrane-Based WFI System

SHANGHAI CHONGYANG WATER TREATMENT EQUIPMENT CO.,LTD
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Membrane-Based WFI System

Brand Name : CHONGYANG

Model Number : CY-WFI-300Liter/Hour

Certification : ISO ,CE

Place of Origin : China

MOQ : 1

Price : Negotiation

Payment Terms : L/C, T/T

Supply Ability : 100 Sets/Months

Delivery Time : With 30-40 Days

Packaging Details : According to export standard

Material : SS316L

Stages : Double RO +EDI+ Ultrafiltration

Valve : Diaphragm Valve

Pump : Grundfos, CNP

Conductivity : 1.3μS/cm

Requested Feed Water : Purified Water System

Product Name : Ultrafiltration WFI Water

Standard : FDA,USP,cGMP,GMP

Pipeline Material : BPE,SS

Capacity : 100L/H -10,000L/H

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Membrane-Based WFI System

Product Overview: The Membrane-Based WFI System is designed for pharma Water for Injection production using double-pass RO, EDI and ultrafiltration technology. It provides stable water quality, lower energy consumption and GMP-compliant operation for modern pharmaceutical manufacturing.

Applications

This system is widely used in pharma manufacturing, biotechnology production, sterile preparation, laboratory research and medical industries where high-purity Water for Injection is required for injection, cleaning and process water applications.

Process Flow

Pretreatment → Double Pass RO → EDI → Ultrafiltration (UF) → Storage Tank → Distribution Loop (SS316L) → Point of Use

Technical Parameters

Item Specification
Capacity 100–10,000 L/H
Conductivity ≤1.1 µS/cm @25°C
TOC ≤500 ppb
Endotoxin ≤0.25 EU/ml
Bacteria <10 CFU/100 ml
Material SS316L, internal Ra <0.4 μm
Control System PLC + HMI, or Schneider optional

Configuration List

The system includes multimedia filter, activated carbon filter, water softener, double-pass RO membranes, EDI module, ultrafiltration membrane for endotoxin removal, sanitary pumps, UV sterilizer, ozone system, SS316L storage tank and automatic PLC control system.

Project Cases

Our membrane-based WFI systems have been applied in pharmaceutical factories in Southeast Asia, the Middle East and Europe, helping customers achieve stable WFI production, GMP validation and continuous operation.

Certifications & Standards

The system is designed according to GMP, FDA, USP, EP and WHO requirements. Optional IQ/OQ/PQ validation support and complete documentation can be provided for audit and compliance needs.

FAQ

Q: Is membrane-based WFI acceptable under GMP?
A: Yes. It can be accepted with proper system design, validation and water quality control strategy.

Q: What are the advantages compared with distillation?
A: Lower energy consumption, compact design, faster startup and flexible operation.

Q: Can the system be customized?
A: Yes. Capacity, materials, control system and validation documents can be customized.

Membrane-Based WFI System

Membrane-Based WFI System

FAQ:

1.Question: Which process do you adopt ?

Answer:Usually we will be according to what your raw water quality and your requested water requirement .

2. Question:Can you customize For me?

Answer :Yes. We can manufacture according your requirement , we can even design appearance of equipment .

3.Question: What standards is the Pharmaceutical Purified Water System ?

Answer: Usually there are five standards in this pharmaceutical industry , FDA,cGMP ,GMP ,USP, Japanese .

4.Question:How long is the Delivery time ?

Answer: Usually the delivery time is 35 -40 Days .


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