Bevigard-P Cartridge Filters
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Overview
Specifications
Ordering Information
Documentation
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Categories
| Biopharmaceutical Manufacturing > Upstream Processing > Multi-use Processing Systems > NovAseptic |
Description
These versatile, composite depth and surface-type filters retain contaminant within the depth matrix of the borosilicate glass microfiber medium, as well as on the surface of the mixed cellulose esters membrane.
They combine high dirt-holding capacity with excellent throughput. The two filtration stages, depth and membrane, offer high dirt-holding capacity with high retention efficiency to protect final filters such as Vitipore™ II and Vitipore II Plus. Bevigard™-P filters can be repeatedly hot-water regenerated, thus providing highly cost-efficient filtration.
Bevigard-P filters are manufactured in a facility whose Quality Management System is approved by an accredited registering body to the ISO® 9000 Quality Systems Standard.
Typical Applications
Bevigard-P Cartridge Filters are designed for all types of application where both high adsorption capacity and fine filtration are needed, for example with water, wine and other beverages.
| per 10-inch Cartridge | |
| Materials of Construction | |
| Filter | Mixed Cellulose Esters (MCE) |
| Prefilter | Borosilicate Glass Fiber (BGF) |
| Structural Components | Polypropylene |
| Filter Supports | Spun bonded polypropylene |
| O-rings | Silicone (SI) |
| Nominal Pore Size | |
| CGW3 | 1.0 / 0.2 µm |
| CGW6 | 1.0 / 0.5 µm |
| CGW9 | 2.0 / 1.2 µm |
| Filtration Area | 0.46 m² |
| Maximum Differential Pressure, bar (psid) | 3.5 bar (50 psid) @ 25 °C |
| Maximum Operating Temperature | 80° C |
| Sterilization | 10 autoclave cycles or SIP @ 121 °C for 30 min |
| Sanitization | 30 min with hot water @ 80 °C |
| Good Manufacturing Practices | These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. |
| Non-Fiber Releasing | Component materials meet the "non-fiber releasing" criteria as defined in 21 CFR 210.3 (b) (6). |
| Component Material Toxicity | Component materials meet the criteria of the USP <88> Reactivity Test for Class VI Plastics. These products meet the requirements of the USP <88> Safety Test, utilizing a 0.9% sodium chloride extraction. |
| Indirect Food Additive | All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. |
| Certificate of Quality | Each cartridge is shipped with a Certificate of Quality which summarizes our stringent manufacturing and quality standards. |
Typical Clean Water Flow Rate vs Pressure Drop
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10-inch Cartridge Filter with Bevigard™-P Media