SaiPress® PVDF Sterilizing-grade Hydrophilic Disk Filter

Cat. No.	Specification	Unit	Price	Quantity
FCM1530450-01	Filter Size: 2.8m², Membrane Pore Size: 0.45μm, Connector type: Luer(female)in Luer(male)out	1 per package	Inquiry
FCM1530450-02	Filter Size: 2.8m², Membrane Pore Size: 0.45+0.22μm, Connector type: Luer(female)in Luer(male)out	1 per package	Inquiry

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Product Description

Product Description

Saipress® PVDF sterilizing-grade hydrophilic filter is suitable for sterile filtration of various biopharmaceutical products. It is made of PVDF membrane with symmetric pore structure, uniform hydrophilicity, high porosity, and extremely low protein adsorption.

Product Features
• High porosity, extremely low protein adsorption
• Low extractables and broad chemical compatibility
• 100% integrity test ensures sterilization efficacy

Product applications
• Filtration of sterile APIs and ophthalmic preparations
• Filtration of Small Volume Parenterals (SVP) and Large Volume Parenterals (LVP)
• Filtration of high-purity chemicals, intermediates, strong acid and oxidizing liquids
• Filtration of vaccines, biologics, blood products

Available Connector Type:
• 226 connectors
• 222 connectors

More Details

SaiPress® Sterilizing-grade Hydrophilic Filters

Product Details

Product Type

Sterilization Filtration Solution

Specifications

Filter membrane: PVDF
Supporting layer: Polypropylene
Housing: Polypropylene
Central core: Polypropylene
Filter membrane: PVDF
Supporting layer: Polypropylene
Housing: Polypropylene
Central core: Polypropylene
Connector: Polypropylene
O-ring: Silicone/EPDM/FKM
Outer Diameter: 69 mm
Inner Diameter: 33 mm
Length: 5 - 40 inch
Effective filtration area (m²): Single layer: 0.65m²/10inch；Double layer: 0.55m²/10inch
Forward: 5.2 bar @ 25°C,2.7 bar @ 80°C
Reverse: 2.1 bar @ 25°C
SIP Sterilization method: 124°C, 30min, 30 times; 134°C, 20min, 30 times
Autoclave Sterilization method: 124°C, 30min, 30 times; 134°C, 20min, 30 times

Quality Control:
• ISO 9001: 2015 Quality Management System;
• 100% integrity testing;
• Full traceability of filter;
• All materials comply with CFR 21 requirements;
• Validated bacterial retention efficiency"