Sterilizing Grade PPS Polyethersulfone Cartridges
Sterilizing Grade PPS Polyethersulfone Cartridges
SKU:PLE-696dbe
Premium PPS Polyethersulfone Cartridges for pharmaceutical sterility. Double-layered membrane for superior retention. Ideal for vaccines and biologicals.
Regular price
$129.99
Regular price
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$129.99
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Sterilizing Grade PPS Polyethersulfone Cartridges
$129.99
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Sterilizing Grade PPS Polyethersulfone Cartridges
$129.99
Quantity: 1
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Our PPS Grade Polyethersulfone Cartridges are specially designed for the pharmaceutical industry, featuring a double-layered PPS membrane for enhanced retention efficiency. Ideal for sterile fill applications in SVPs and biological products, these cartridges offer low binding characteristics, making them suitable for filtering protein solutions like vaccines. 100% integrity tested and validated to meet stringent industry standards.
Product Specifications
Applications 0
Final Filtration of:DiagnosticsLVPs & SVPsWFI WaterVaccinesBiologicalsMedications
Construction Materials Center Core Material
Polypropylene
Construction Materials End Caps Material
Polypropylene
Construction Materials Filtration Media
Dual Layered Polyethersulfone
Construction Materials Filtration Media Support Material
Polypropylene
CONSTRUCTION MATERIALS OUTER SUPPORT CAGE Material
Polypropylene
Construction Materials O Rings Material
Buna | EP | PTFE® Encapsulated Silicone | PTFE® Encapsulated Viton® | Silicone | Viton®
Construction Materials Sealing Method
Thermal Bonding
Dimensions Filtration Area Per 10 Length
7.0 ft² | 0.65 m²
Dimensions Nominal Length
5 to 40 in | 12.7 to 101.6 cm
Dimensions Nominal Outside Diameter
2.75 in | 7.0 cm
Extractables 0
The levels of bacterial endotoxins in aqueous extracts from Pharmaceutical Grade Filters are below the USP24 limits defined in Water for Injection (â¤0.5 EU/ml). Pharmaceutical Grade Filters typically exhibit low levels of non-volatile residues.
Fda Compliance 0
The materials used to construct Pharmaceutical Grade filters meet the requirements listed by the FDA as appropriate for use in articles intended for repeated food contact as specified in Title 21 CFR sections 174.5, 177.1500, 177.1520, 177.1630, 177.2440 and 177.2600 as appropriate. PPS filters comply with Title 21 CFR sections 210.3 (b)(6) and 211.72, for non-fiber releasing filters.
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 10-inch cartridge element. The test fluid is water at ambient temperature. Extrapolation for housings with multiple elements and higher pressure drops is acceptable, but as flows increase the pressure drop of the housing becomes more apparent.
Integrity Test Information Air Diffusion Rate
⤠15 cc/min at 60 psi | ⤠15 cc/min at 4137 mbar
Maximum Operating Parameters Forward Differential Pressure At 20
50 psi | 3.4 bar
Maximum Operating Parameters Operating Temperature At 10 Psid 06
180 ºF | 82 ºC
Maximum Operating Parameters Recommended Change Out Pressure
35 psid | 2.4 bar
Maximum Operating Parameters Reverse Differential Pressure At 20
40 psi | 2.7 bar
Quality Assurance 0
Pharmaceutical Grade Filters are manufactured using current Good Manufacturing Practices under a quality management system that has met ISO 9001 standards. Each Pharmaceutical Grade Filter is assigned a lot code to ensure traceability of the data and materials used in the manufacturing process. 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 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.
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 PPS cartridges are available from Critical Process Filtration, Inc.
Sanitization Sterilization Filtered Hot Water
194 ºF | 90 ºC
Sanitization Sterilization In Line Steam
275ºF (135ºC), 30 min, multiple cycles
Specifications 316 Ss Ring
No Ring
Specifications Cartridge Length
4.875 in | 12.4 cm
Specifications End Caps
020 O-ring / Plug | 213/119 Internal O-ring / Plug | 213/119 Internal O-ring DOE | 2-222 O-ring / Flat | 2-222 O-ring / Plug | 2-222 O-ring / Spear | 2-222 O-ring 3 Tab / Flat | 2-222 O-ring 3 Tab / Spear | 2-223 O-ring / Flat | 2-223 O-ring / Spear | 2-226 O-ring / Flat | 2-226 O-ring / Spear | Flat Gasket / Plug | Flat Gasket, DOE
Specifications Flow Rate
1.1 gpm | 4.16 lpm
Specifications Pore Size
0.03 µm
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 Pharmaceutical Grade filters are non-toxic and meet the requirements for the MEM Elution Cytotoxicity Test and USP24 Plastic Class V1 121ºC Test.
Validation 0
PPS grade cartridges are validated using modified HIMA protocols at a challenge level of 107 organisms per cm2 of filter media. (0.22 µm challenged with Brevundimonas diminutal) (0.45 µm challenged with Serratia marscecens) (0.65 µm challenged with Saccharomyces cerevisiae). Validation Guide is available for 0.22 micron to meet regulatory requirements.