| per 10-inch Cartridge |
| Materials of Construction |
| Filter | Mixed Cellulose Esters |
| Structural Components | Polypropylene |
| Filter Supports | Polyester |
| O-rings | Silicone |
| Nominal Pore Size, µm |
| W03 | 0.2 |
| W06 | 0.5 |
| W19 | 1.2 |
| Filtration Area, m2 | 0.8 |
| Maximum Differential Pressure, bar (psid) | 3.5 (50) @ 25 °C |
| Maximum Operating Temperature, °C | 80 |
| 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 Device 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. |
