Product Details
PVDN - Hydrophilic PVDF Membrane Cartridge
Brand DuoFluor
Masterfilter PVDN filter cartridges are manufactured from an inherently hydrophilic PVDF membrane that offers a broad chemical and temperature resistance. Characterised by its low protein binding properties, the PVDN series is ideal for bioburden reduction, clarification and sterilisation of pharmaceutical and biological solutions. The PVDN cartridges are available in multiple pore sizes with single-layer PVDF membrane. The membranes are easily wettable and fully integrity testable to meet the pharmaceuticals levels for sterility assurance.
Features Benefits
- Inherently hydrophilic membrane
- Low in protein binding, extractables and non-fibre shedding
- Easily wettable
- High flowrate with low pressure drop
Markets
- Pharmaceuticals and Biologicals
- Water
- Chemicals
Technical Specification
Materials of construction
Membrane: Hydrophilic Polyvinylidene fluoride (PVDF)
Support layers: Polypropylene
Inner core: Polypropylene
Outer cage: Polypropylene
End caps: Polypropylene
O-Rings: EPDM, Silicone, Viton
Operating parameters
Max. differential pressure: 6.9 bar at 25 °C, 4.0 bar at 60 °C, 2.4 bar at 80 °C
Steam sterilisation: 20 cycles for 30 min at 125 °C (< 0.3 bar, 5 psi) in forward direction
Autoclave: 30 cycles for 30 min at 125 °C
Filtration area 10” module : 0.58 m²
Applications
- Fermentation
- LVP (Large Volume Parenterals)
- SVP (Small Volume Parenterals)
- Pharmaceutical Water Treatment
- Ophthalmics
- API (Active Pharmaceutical Ingridients)
- Process Water
- Municipal
- Power Utilities
- Raw Materials Clarification
- Raw Materials Intermediate Polishing
- Final Product Filtration
Filter Properties
- Tested with Brevundimonas Diminuta (ATCC 19146) at 107 CFU/cm² according with ASTM-F838
- Cartridge is marked with unique serial number for identification and traceability
- All components meet the criteria for Non-Fibre releasing as defined in 21 CFR 210.3 (b) (6)
- PVDN Duofluor is manufactured under ISO 9001:2015 GMP
- Extraction samples < 0.25 EU/mL as determined by the LAL, USP <85>
- Meets the USP <88> Biological Toxicity Reactivity Test in vivo for Class VI-121 °C in plastics
- Meets USP <87> in vitro cytotoxicity test and autoclaved filter effluent meets the USP <788> for LVP
- All components meet the FDA indirect food additive requirements cited in 21 CFR 177-182
