Bevigard-M Cartridge Filters

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概述
规格
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相关产品和应用
相关产品,按下列排序: Application Facete
| Fermentation Solutions | 
| Dialysis and Filtration | 
相关产品,按下列排序: Brand Facete
| Bevigard™ | 
种类
| Biopharmaceutical Manufacturing > Upstream Processing > Multi-use Processing Systems > NovAseptic | 
Description
Used in final stage prefiltration applications, these versatile surface-type products retain contaminant on the mixed cellulose esters membrane.
Used as final filter for bioburden reduction, they offer an excellent efficiency of microorganism removal. Because of their structure, Bevigard™-M cartridge filters offer the best protection of final sterilizing-grade filters such as Vitipore™ II and Vitipore II Plus, saving money on this critical final step. 
Bevigard-M filters can be repeatedly hot water regenerated providing highly cost effective filtration.
They 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-M cartridge filters are designed for beverage prefiltration applications or final filtration stages such as sterilizing grade filter protection or bioburden reduction of water, wine or other beverages.
| per 10-inch Cartridge | |
| Materials of Construction | |
| Filter | Mixed Cellulose Esters (MCE) | 
| Structural Components | Polypropylene | 
| Filter Supports | Polyester | 
| O-rings | Silicone (SI) | 
| Nominal Pore Size | |
| W03 | 0.2 µm | 
| W06 | 0.5 µm | 
| W19 | 1.2 µm | 
| Filtration Area | 0.8 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. | 

 


 
  

 
 
