millipore,
密理博,KWSSA02NN3,Opticap XL 2 with Milligard - 2" 0.5/0.2 µm NPT/NPT 3pk
重要规格表
| Description
|
| Catalogue Number | KWSSA02NN3 |
| Trade Name |
|
| Description | Opticap® XL 2 with Milligard® - 2" 0.5/0.2 µm NPT/NPT 3pk |
| Product Information
|
| Format | Double Layer |
| Device Configuration | Capsule |
| Connections, Inlet/Outlet | NPT/NPT |
| Housing Material | Polypropylene (PP) |
| Maximum Differential Pressure, bar (psid) | 3.5 bar (50 psid) @ 25 °C |
| Maximum Inlet Pressure, bar (psi) | 5.5 bar (80 psi) @ 23 °C; 2.75 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C |
| European Pressure Equipment Directive | EMD millipore Corporation® certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark. |
| Good Manufacturing Practices | These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. |
| Quality Level | MQ400
|
| Biological Information
|
| Bacterial Endotoxins | Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test |
| Media | Milligard® |
| Sterilization | 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable |
| Physicochemical Information
|
| Pore Size | 0.5 / 0.2 µm |
| Inlet Connection | NPT |
| Outlet Connection | NPT |
| Gravimetric Extractables | The extractables level was equal to or less than 15 mg per capsule 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. |
| Maximum Inlet Pressure (psig) | 80 psig |
| Maximum Inlet Temperature | 25 °C |
| Non-Fiber Releasing | This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6). |
| USP Bacterial Endotoxins | A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. |
| Dimensions
|
| Cartridge Nominal Length | 2 in. (5 cm) |
| Device Size | 2 in. |
| Inlet Connection Diameter | 1/4 in. |
| Nominal Pore Size | 0.5 / 0.2 µm |
| Outlet Connection Diameter | 1/4 in. |
| Materials Information
|
| Chemistry |
- Mixed Cellulose Esters (MCE)
|
| Device Material |
|
| Seal Material | Silicone (SI) |
| Support Material | Polyester |
| Vent Cap Material | Polypropylene (PP) |
| Packaging Information
|
| Material Size | 3 |
| Material Package | Double Easy-Open bag |
