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Membrane-Based WFI System
Detail produk:
| Tempat asal: | Cina |
| Nama merek: | CHONGYANG |
| Sertifikasi: | ISO ,CE |
| Nomor model: | CY-WFI-300Liter/Jam |
Syarat-syarat pembayaran & pengiriman:
| Kuantitas min Order: | 1 |
|---|---|
| Harga: | negotiable |
| Kemasan rincian: | Sesuai standar ekspor |
| Waktu pengiriman: | Dengan 30-40 Hari |
| Syarat-syarat pembayaran: | L/C, T/T |
| Menyediakan kemampuan: | 100 set/bulan |
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Informasi Detail |
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| Bahan: | SS316L | Tahapan: | RO Ganda +EDI+ Ultrafiltrasi |
|---|---|---|---|
| Katup: | Katup Diafragma | Pompa: | Grundfos, CNP |
| Daya konduksi: | 1,3μS/cm | Air Umpan yang Diminta: | Sistem Air Murni |
| Nama Produk: | Air WFI Ultrafiltrasi | Standar: | FDA,USP,cGMP,GMP |
| Bahan Pipa: | BPE,SS | Kapasitas: | 100L/JAM -10.000L/JAM |
Deskripsi Produk
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
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.
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 .