Place of Origin:

China

Brand Name:

CHONGYANG

Certification:

ISO ,CE

Model Number:

CY-WFI-300Liter/Hour

Minimum Order Quantity:

Price:

Negotiation

Packaging Details:

Export standard

Delivery Time:

With 30-40 Days

Payment Terms:

L/C, T/T

Supply Ability:

100 Sets/Months

Material:

SS316L

Stages:

4-6 Effects

Conductivity:

1.3μS/cm

Requested Feed Water:

Purified Water System

Standard:

FDA,USP,cGMP,GMP

Pipeline Material:

BPE,SS

Membrane-Based WFI System

Name: Membrane-Based WFI System
Brand: Shanghai ChongYang Water Treatment Equipment CO.,LTD.
SKU: CY-WFI-300Liter/Hour
Availability: InStock

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 pharma manufacturing.

Applications

This system is widely used in pharmaceutical 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.

Company name : Shanghai Chongyang Water Treatment Equipment CO.,LTD