Life Science Filter
Protecting Life with Biosecurity Filtration
Hydrophilic Filter NOVAC HC
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NOVAC HC series features a membrane made of hydrophilically modified polytetrafluoroethylene (PTFE), offering excellent chemical compatibility and suitable for filtering pharmaceutical liquids containing organic solvents. NOVAC HC series pre-filters are available in disc, capsule, and cartridge formats, meeting the requirements of the entire process from R&D, pilot-scale to production
Product Features
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Hydrophilic membrane, no pre-wetting required
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Excellent chemical compatibility (pH 1-14)
Typical Application
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Pre-filtration of pharmaceutical liquids containing organic solvents
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Pre-filtration of disinfectant and cleaning solutions
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Pre-filtration of antibiotic solutions
Based on the document "image_ba5126.png", here is the technical specification summary organized for easy selection:
NOVAC HC Series Filter Technical Specifications
1. Filter Types and Dimensions
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Capsule Filter:
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Nominal sizes: S, 2.5, 5, 10
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Filtration Area: 180cm2 (for S); 0.073 m2 (for 2.5); 0.23 m2 (for 5); 0.63 m2 (for 10)
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Cartridge Filter:
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Dimensions (phi63, phi70) with respective filtration areas (m2):
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2.5 inch: 0.12 / 0.17
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5 inch: 0.25 / 0.35
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10 inch: 0.50 / 0.70
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20 inch: 1.0 / 1.40
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30 inch: 1.5 / 2.10
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2. General Specifications
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Filter Aperture: 0.45 μm
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Materials of Construction:
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Support Layer, Shell, End Cap, Fin, Adaptor: PP
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Sealing Ring: Silicon / Fluoroelastomer / EPDM / FEP+FKM
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Membrane material: Hydrophilic PTFE
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Hot-Melt Technology: Adhesive free technology
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3. Maximum Differential Pressure
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Capsule Filter:
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Forward: 5 bar (72.5 psi) @20°C / 3 bar (43.5 psi) @50°C (for L, M); 4 bar (58 psi) @20°C / 2 bar (29 psi) @50°C (for S)
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Backward: 2 bar (29 psi) @20°C / 1.5 bar (22 psi) @50°C
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Cartridge Filter:
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Forward: 5 bar (72.5 psi) @20°C / 2 bar (29 psi) @80°C
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Backward: 2 bar (29 psi) @20°C
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4. Sterilization and Regulatory Compliance
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Sterilization:
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Autoclave: 134°C * 30min * 25 times
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Online steam sterilization (Cartridge only): 134°C * 30min * 25 times (delta p <= 0.3 bar)
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Component Material Toxicity: Meets USP <88> Biological Reactivity for Class VI
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Ingredient Material Toxicity: Meets USP <88> Class VI plastics reaction test standards
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Cleanliness: Complies with FDA 21 CFR 211.72 and 210.3(b)(5)(6) for fiberless shedding filters, and USP <788> for insoluble particulate levels in the rinse solution
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Bacterial Endotoxin: Aqueous extraction contains < 0.25 EU/mL, meeting USP <85> requirements
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Integrity: Each cartridge/filter passes 100% integrity testing before it leaves the factory
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Production environment: All produced in 100,000 class clean room
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Product Parameters
Typical Applications
Related components
Related Equipment
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Contact
Hotline: (+86)400-820-6150
Email: marketing@feature-tec.com
Address: 8/F, Block A, Building 3, Tianhua Information Technology Park, 299 Longcao Road, Xuhui District, Shanghai