Critical Process Disposable Media Filter Capsules - Nylon Membrane 0.45 µ
Critical Process Disposable Media Filter Capsules - Nylon Membrane 0.45 µ
SKU:PLE-cf36a0
Premium disposable media filter capsules for precise and cost-effective filtration in electronics and high purity industries.
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            $59.99
          
      
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                The Critical Process Disposable Media Filter Capsules are meticulously engineered for cost-effective filtration needs, offering a wide range of pleated and depth media options. Designed for small flow and encapsulated disposable cartridge requirements, these capsules adhere to stringent quality standards suitable for liquids and gas applications. With a Grade designed for electronics and high purity industries, these capsules boast a Nylon Membrane with a 0.45 µ micron rating, ensuring efficient filtration and exceptional cleanliness. Each cartridge module undergoes thorough testing and validation to meet FDA acceptance criteria and USP class 6 toxicology extractable tests, ensuring optimal performance and durability.
              
Product Specifications
                  Construction Materials Filtration Media 
                
                Nylon
              
                  Construction Materials Filtration Media Support Material 
                
                Polypropylene
              
                  Construction Materials Grade 
                
                Electronic
              
                  Construction Materials Housing 
                
                Polypropylene
              
                  Construction Materials Note 
                
                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.
              
                  Construction Materials Sealing Method 
                
                Heat - Fused
              
                  Construction Materials Support Components Material 
                
                Polypropylene
              
                  Filtration Media 0 
                
                Nylon Membrane - NMNM Capsules are hydrophilic Nylon membrane, able to remove particles below the rated pore size of the membrane. These capsules exhibit superior retention, used across the beverage, electronic and pharmaceutical industries. Applications include high purity water, esters, solvents, cosmetics, alcohols, ketones, glycols and many others. PNM grade Nylon capsules are designed to be used as sterilizing grade capsules for the pharmaceutical industry. Nylon capsules see broad service in sterile fill applications in SVPs and as bio burden management filters in LVPs. Media and service liquid filtration are other common applications for this capsule. Nylon is particularly suited for the filtration of solvents because of itâs broad compatibility and low level of extractables. 100% integrity tested.
              
                  Flow Rate 0 
                
                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.
              
                  Integrity Test Information Air Diffusion Rate 
                
                ⤠4.3 cc/min at 20 psi | ⤠4.3 cc/min at 1378 mbar
              
                  Maximum Operating Parameters Forward Differential Pressure At 20 
                
                50 psi | 3.4 bar
              
                  Maximum Operating Parameters Gases Operational Pressure At 20c 
                
                60 psi | 4.1 bar
              
                  Maximum Operating Parameters Liquid Operational Pressure At 20c 
                
                80 psi | 5.5 bar
              
                  Maximum Operating Parameters Operating Temperature At 30 Psi 14 
                
                110 ºF | 43 ºC
              
                  Maximum Operating Parameters Recommended Change Out Pressure 
                
                20 psid | 2.4 bar
              
                  Maximum Operating Parameters Reverse Differential Pressure At 20 
                
                40 psi | 2.7 bar
              
                  Pore Size Removal Ratings 
                
                0.03 to 100 µ
              
                  Quality Standards 0 
                
                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 âreal timeâ 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.
              
                  Sanitization Sterilization Autoclave 
                
                250ºF (121ºC), 30 min, multiple cycles
              
                  Sanitization Sterilization Chemical Sanitization 
                
                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.®.
              
                  Sanitization Sterilization Filtered Hot Water 
                
                194 ºF | 90 ºC
              
                  Sanitization Sterilization Inlet Outlet Options 
                
                1/2" Female NPT | 1/2" Male NPT | 1/4 Male NPT | 1/4" Female NPT | 3/8" Female NPT | Hose Barb | Sanitary
              
                  Sanitization Sterilization Pre Sterilized 
                
                Not Sterilized | Pre- Sterilized
              
                  Sanitization Sterilization Vent Drain 
                
                Standard with Luer- Lok¨ ports and caps
              
                  Specifications Capsule Length 
                
                2 in | 5 in | 10 in | 23 in | 30 in
              
                  Specifications Filter Mediamembrane 
                
                Nylon Membrane
              
                  Specifications Flow Rate 
                
                1.62 gpm
              
                  Specifications Grade Definition 
                
                Designed to meet the special needs of the electronics and high purity chemical industries. To minimize extractables, each cartridge module is pulse, power flushed until the rinse effluent reaches 17+ megohm-cm and less than 3 ppb TOC. Each cartridge module is also individually tested.
              
                  Specifications Micron Rating 
                
                0.45 µ
              
                  Total Performance 0 
                
                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.
              
                  Usp Biosafety 0 
                
                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.
              
                  Validation 0 
                
                P - grade capsules are validated using modified HIMA protocols at a challenge level of 107 organisms per cm2 of filter media.F & E - grade capsules are validated using modified HIMA protocols at a challenge level of 106 organisms per cm2 of filter media.G - grade capsules are validated using modified HIMA protocols at a challenge level of 104 organisms per cm2 of filter media.(0.22 µm challenged with Brevundimonas diminuta) (0.45 µm challenged with Serratia marscecens) (0.65 µm challenged with Saccharomyces cerevisiae).