Industry’s Filtration Partner
Complete Range of Disposable Media Filter Capsules Engineered and Manufactured for Cost Effective Filtration

CP capsules are designed and manufactured by Critical Process for small flow and encapsulated disposable cartridge requirements. CP capsules are offered in a wide range of pleated and depth medias and offered in four grades; general, food / beverage, electronic and pharmaceutical. Each Capsule has been designed to hold the maximum amount of filter media that can be completely and effectively utilized in a capsule. CP capsules lower the cost of filtration and reduce the need for high cost metallic housings. They are well suited for liquids and gas applications with the same attention to quality, traceability, validation and testing.

Certificate of Quality Assurance is provided with every Food, Electronic and Pharmaceutical Capsule
Unit of Measure

Specifications

Grade Definition

N/A 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.

Filter Media/Membrane

N/A Nylon Membrane

Micron Rating

N/A 5.0 µ

Capsule Length

N/A 2
5
10
23
30

Construction Materials

Housing

N/A Polypropylene

Grade

N/A Electronic

Filtration Media

N/A Nylon

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.

Maximum Operating Parameters

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

Pore Size

Removal Ratings1 N/A 0.03 to 100 µ

Sanitization / Sterilization

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

Filtration Media

N/A Nylon Membrane - NM

NM
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 it’s broad compatibility and low level of extractables. 100% integrity tested.

Validation

N/A 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).

USP Biosafety

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.

Quality Standards

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.

Total Performance

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.

Flow Rate

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.

  • 1 Continue to the media specifications for the specific pore size available
  • 2 CP capsules are not to be used in steam.
  • 3 CP capsules are offered in both a non and pre sterilized grade.