3M™ Zeta Plus™ LP Series Filter Cartridge is our positively charged resin system that pulls negatively charged contaminants from biological fluids. Cartridges are composed of inorganic filter aid, cellulose and feature multi‐zone microporous membrane and Advanced Pleat Technology.
Nutzen und Einsatzmöglichkeiten von 3M™ Zeta Plus™ LP Serie Filterkerze, Z12DD90LP OCTAPHARMA, 12 Zoll, 2/Box
- Allows for scalable configurations for pilot testing and scale-up using the same materials as full-size systems.
- FDA Drug Master File (DMF) and USP Class VI Reactivity compliance eases validation and regulatory submission.
- Filter media retains contaminants by mechanical entrapment and electrokinetic adsorption.
- High contaminant holding capacity provides economical filtration and reliable particle reduction.
- High purity, pre-extracted cellulose provides lower β-glucan extractable levels.
- Self-contained, single-use disposable cartridge modules allows reduced labour for changeouts and eliminates cleaning validation.
For high contaminant holding media, economical filtration and reliable particle reduction use 3M™ Zeta Plus™ LP Series Filter Cartridge.Our family of depth filters retains contaminants by a combination of mechanical entrapment and electrokinetic adsorption. LP cartridges feature a positive charge that pulls out more negatively charged contaminants compared to a mechanical filtration mechanism alone, and feature high purity, pre-extracted cellulose providing lower β-glucan extractable levels.Offering scalable capsule and cartridge filter configurations this range allows you to pilot test and scale-up using the same materials as you would for full-scale systems.These cartridge filters are manufactured to meet the strict requirements specified in 3M’s Drug Master File (DMF) including product control and traceability. They meet the requirements of USP Class VI Biological Reactivity Tests and Certificates of Quality are included with every filter. Providing this vital compliance documentation and traceability eases validation and regulatory submissions.
