BioPro® KSO 5", 10", 20", 30"
The BioPro® KSO capsule filters are designed for protecting your critical and high value downstream systems.
These help in significant reduction of bioburden and complete removal of particulate contamination and are ideal for applications which do not require sterilization but where reduction in bio load in the process fluid is the objective.
These improve the process efficiency by reducing filter sizing and prolonging life of expensive sterilizing filters.
- Validated for high bio-burden reduction
- High flow rates
- High throughput
- Low protein binding
- No media migration
- Biologically inert
- Easy installation
- Clarification of cell harvest
- Buffer filtration
- In process protein filtration
- Prefiltration to sterile filtration
- Prefiltration to virus filtration
Construction | |||||
Membrane | Hydrophilic PES | ||||
Final Filter Pore Size (Nominal) | 0.1µm, 0.2µm, 0.45µm | ||||
Support Layers | Polypropylene | ||||
Body and Core | Polypropylene | ||||
Size | |||||
Size |
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Effective Filtration Area (Nominal) |
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Dimension (End to End) - 1½" Sanitary Flange Inlet ½" Hose Barb Outlet |
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Dimension (End to End) - ¾" Sanitary Flange I/O |
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Dimension (End to End) - 1½" Sanitary Flange I/O |
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Dimension (End to End) - ½" Single Step Hose Barb I/O |
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Dimension (End to End) - 1" Hose Barb I/O |
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Operational Radius (with Vent/ Drain) |
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Dimension (End to End) - 3/8" Hose Barb I/O |
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Vent and Drain | ¼" Hose Barb with Silicone "O" rings | ||||
Integrity Testing / Retention | |||||
Bacterial Retention |
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Bubble Point (with water) |
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Operational | |||||
Max. Operating Temperature | 80 °C @ < 30 psi (2 Kg/cm²) | ||||
Max. Differential Pressure | < 60 psi (4 Kg/cm²) @ 30° C | ||||
pH Compatibility | Compatible with 1-14 pH | ||||
Sterilization By Gas | Sterilizable by Ethylene Oxide | ||||
Sterilization By Autoclave | Autoclavable at 125°C for 30 minutes , 25 cycles and it cannot be In-line steam sterilized | ||||
Shelf Life | 3 years after EO sterilization | ||||
Assurance | |||||
Toxicity | Passes Bioreactivity test, Invivo, as per USP <88> for Class VI plastics | ||||
Bacterial Endotoxin | Aqueous extracts exhibit < 0.25 EU/ml as established by LAL Test | ||||
Bioburden | Bioburden level is < 1000 cfu/filter device as per ISO 11737-1 : 2018 | ||||
Non Fiber Releasing | Complies with USFDA CFR Title 21, 210.3 (b) (6) | ||||
Particle Release | The filtrate complies with USP <788> test for particulatematter in injections | ||||
Indirect Food Additive | Passes as per USFDA 21 CFR 177.1520 | ||||
Extractables with WFI | Passes test as per USP | ||||
Good Manufacturing Practice | These products are manufactured in a facility which adheres to Good Manufacturing Practices. | ||||
Oxidizable Substances | Within limits as specified in USP | ||||
Quality Management System | ISO-9001 Certified | ||||
USFDA | DMF No. 015554 |
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* T-line is not available in 5" Capsule filter
* T-line Capsule filter are available with 1½" Sanitary Flange I/O only
**3/4" Sanitary Flange end connection is available only in 5" and 10" capsule filters
***1" Hose Barb is not available in 5" capsule filters
Example :
LBKO | 56 | 01 | EE | X | X | 1 | 01 |