Grade Definition |
N/A Designed for general purpose use at an effective cost. Each module is rinsed with 17+ megohm-cm water to remove potential extraneous manufacturing debris. Each cartridge module is individually tested for integrity. |
Filter Media/Membrane |
N/A Polyethersulfone Membrane |
Micron Rating |
N/A 0.50 µ |
Capsule Length |
N/A
2 5 10 23 30 |
Flow Rate |
N/A 4.54 gpm |
Housing |
N/A Polypropylene |
Grade |
N/A General |
Filtration Media |
N/A Polyethersulfone |
Filtration Media Support Material |
N/A Polypropylene |
Support Components Material |
N/A Polypropylene |
Sealing Method |
N/A Heat - Fused |
Note |
N/A All materials of construction are FDA accepted. Final assemblies have been validated to pass USP class 6 Toxicology extractable tests, oxidizable substances for plastics, endotoxin level and other quality tests. |
Liquid Operational Pressure at 20ºC |
N/A 80 psi5.5 bar |
Gases Operational Pressure at 20ºC |
N/A 60 psi4.1 bar |
Forward Differential Pressure at 20ºC |
N/A 50 psi3.4 bar |
Reverse Differential Pressure at 20ºC |
N/A 40 psi2.7 bar |
Operating Temperature at ≤30 psi (1.4 bar) in Water. |
N/A 110 ºF43 ºC |
Recommended Change Out Pressure |
N/A 20 psid2.4 bar |
Filtered Hot Water |
N/A 194 ºF90 ºC |
Autoclave |
N/A 250ºF (121ºC), 30 min, multiple cycles |
Chemical Sanitization2 | N/A Industry standard concentrations of hydrogen peroxide, paracetic acid, sodium hypochlorite and other selected chemicals. Sanitization protocols designed to extend the useful life of CP capsules are available from Critical Process Filtration, Inc.®. |
Pre Sterilized3 | N/A Not Sterilized Pre- Sterilized |
Inlet & Outlet Options |
N/A
1/2" Female NPT 1/2" Male NPT 1/4 Male NPT 1/4" Female NPT 3/8" Female NPT Hose Barb Sanitary |
Vent & Drain |
N/A Standard with Luer- Lok¨ ports and caps |
N/A
Polyethersulfone Membrane - PS |
N/A
P - grade capsules are validated using modified HIMA protocols at a challenge level of 107 organisms per cm2 of filter media. |
N/A The materials used to construct the membrane capsule filters are non-toxic and meet the requirements for the MEM Elution Cytotoxicity Test and USP24 Plastic Class V1 121ºC Test. |
N/A Our goal is to ensure our customers the greatest possible value for their filtration dollar. We achieve both low cost manufacture and high quality by employing state of the art manufacturing equipment. This computer controlled equipment is highly automated, reducing hand operations that compromise quality. Each operation including assembly, testing, cleaning, drying and packaging is done in appropriately rated clean rooms. Critical Process Filtration manages an ISO 9000 facility that produces validated products to rigorous standards. Manufacturing is controlled using sophisticated MRP software that is networked to work stations in manufacturing centers and inspection points. During the manufacturing and inspection processes, data is collected “real time” from machinery and measuring instruments. This allows variable and attribute data to be quickly and easily analyzed to facilitate constant improvements in both quality and cost. |
N/A Critical Process Filtration, Inc.® is a vertically integrated supplier of filtration products and services to industries in which filtration is considered to be a critical part of the manufacturing process. We manufacture a complete line of products to help you achieve all your filtration requirements from a single source. |
N/A See the Flow Rate table in more image which represents typical water flow at a one psi (69 mbar) pressure differential across a single 2 inch capsule 1.0 ft2 (930 cm2) of media with 1/2" FNPT ports. The test fluid is water at ambient temperature. Higher pressure drops is acceptable, but as flows increase the pressure drop of the housing becomes more apparent. |