| per 10-inch Cartridge |
| Materials of Construction |
| Filter Membrane | Polypropylene |
| Structural Components | Polypropylene |
| O-rings (Code 0) | Silicone |
| Gaskets (Code F) | Polyethylene |
| Filter Pore Size, µm | 5 |
| Maximum Differential Pressure, bar (psid) | 4.8 (70) @ 25 °C |
| Sterilization | 5 autoclave cycles or SIP @ 121 °C for 30 min |
| Sanitization | 5 cycles of 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. |