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默克密理博Durapore Cartridge 0.2um濾芯CVDI01TPE
Chemistry：0.2um Hydrophilic Polyvinylidene Fluoride (PVDF)。
| 描述 | |
|---|---|
| 產品編號 | CVDI01TPE |
| 濾膜代碼 |
|
| 產品描述 | Durapore® CVDI Cartridge Filter 10 in. 0.22 µm Code 0 fluoroelastomer |
默克密理博Durapore Cartridge 0.2um濾芯CVDI01TPE
| Device Configuration | Cartridge |
| Maximum Differential Pressure, bar (psid) | Forward: 5.5 bar (80 psid) @ 25 °C; 1.7 bar (25 psid) @ 80 °C; 0.35 bar (5 psid) @ 135 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent |
| Cartridge Code | Code 0 (2-222) O-rings |
| Good Manufacturing Practices | These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. |
| Biological Information | |
|---|---|
| 過濾介質 | PVDF |
| Bacterial Retention | Samples of the Durapore® membrane used in this cartridge were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10? CFU/cm² using ASTM® F838 methodology. |
| 可濕潤性 | 親水性 |
| Physicochemical Information | |
|---|---|
| 孔徑 | 0.2 µm |
| Air Diffusion at 23 °C | ≤13.3 mL/min @ 2.75 bar (40 psig) in water |
| Bubble Point at 23 °C | ≥3100 mbar (45 psig) air with water |
| Gravimetric Extractables | The extractables level was equal to or less than 25 mg per 10-inch cartridge after 24 hours in water at controlled room temperature. |
| Indirect Food Additive | All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food. |
| Non-Fiber Releasing | This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6). |
| 尺寸 | |
|---|---|
| 濾芯長度 | 10 in. (25 cm) |
| 直徑 | 6.9 cm (2.7 in.) |
| 有效過濾面積 | 0.69 m² |
| 濾芯尺寸 | 10 in. |
| 材料信息 | |
|---|---|
| 過濾介質 |
|
| 裝置材質 |
|
| 密封材料 | 氟碳橡膠 |
| 支撐材料 | Polypropylene |
| Packaging Information | |
|---|---|
| Material Size | 1 |
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