ROMICON® SERIES

Based on polysulfone (PS) chemistry, our ROMICON® hollow-fiber cartridges are performance leaders in a variety of industrial biotechnology and general industry applications. ROMICON® cartridges utilize Inside out fibers of wide range of pore sizes and fiber diameters.  The fiber lumen (inner diameter) can be adjusted to best suit the solids tolerance required for each process.

ROMIPRO hollow-fiber cartridges

Designed to meet the most stringent regulations in the pharmaceutical industry, all ROMIPRO cartridge components have passed USP Class VI test guidelines. Each cartridge ships with a Certificate of Quality.

Vinegar and Citrus hollow-fiber cartridges

Made for the acidic environments of vinegar and citrus juice filtration, these cartridges provide high filtration yield with low risk of fiber plugging. They are easy to clean and conform with food processing regulations and practices.
 

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• Protein processing
• Nutraceuticals
• Food
• Juice processing
• Vinegar
• Pharmaceuticals and more

Regulatory Information
U.S. CFR Title 21: Title 21 of the U.S. Code of Federal Regulations (CFR) contains rules and regulations issued by the U.S. Food and Drug Administration (FDA). KMS products used for processing foods and beverages comply with Title 21 as indicated in KMS datasheets. More specifically they comply with Parts 170-199 of Title 21 Subchapter B Food for Human Consumption, which list permitted food additives and associated restrictions. FDA compliance of KMS products is supported by supplier component evaluations, testing, and third-party legal opinions. Abbreviated versions of the legal opinions are available to KMS customers on request.

U.S. CFR Title 21: Title 21 of the U.S. Code of Federal Regulations (CFR) contains rules and regulations issued by the U.S. Food and Drug Administration (FDA). KMS products used for processing foods and beverages comply with Title 21 as indicated in KMS datasheets. More specifically they comply with Parts 170-199 of Title 21 Subchapter B Food for Human Consumption, which list permitted food additives and associated restrictions. FDA compliance of KMS products is supported by supplier component evaluations, testing, and third-party legal opinions. Abbreviated versions of the legal opinions are available to KMS customers on request.
 
USP: The U.S. Pharmacopeia (USP) is a compilation of drug manufacturing standards developed by the U.S. Pharmacopeia Convention. KMS ROMIPRO and SPIRAPRO product components have been tested and certified by a third-party lab to meet the USP Class VI Biological Test for Plastics and Elution Test.

U.S. CFR Title 21: Title 21 of the U.S. Code of Federal Regulations (CFR) contains rules and regulations issued by the U.S. Food and Drug Administration (FDA). KMS products used for processing foods and beverages comply with Title 21 as indicated in KMS datasheets. More specifically they comply with Parts 170-199 of Title 21 Subchapter B Food for Human Consumption, which list permitted food additives and associated restrictions. FDA compliance of KMS products is supported by supplier component evaluations, testing, and third-party legal opinions. Abbreviated versions of the legal opinions are available to KMS customers on request.