KW06A04FF3 | Opticap® XL4 Milligard® 0.5 µm 3/4 in. TC/TC是由上海肯强供应，产品价格优惠，欢迎致电我公司。 手机： QQ：935581225 邮箱：935581225@qq.com
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KW06A04FF3 | Opticap® XL4 Milligard® 0.5 µm 3/4 in. TC/TC
重要规格表
| De |
|
|---|---|
| Catalogue Number | KW06A04FF3 |
| Replaces | KW0604FF3 |
| Trade Name | Opticap® |
| De |
Opticap® XL4 Milligard® 0.5 µm 3/4 in. TC/TC |
| Product Information | |
|---|---|
| Format | Single Layer |
| Device Configuration | Capsule |
| Connections, Inlet/Outlet | 19 mm (3/4 in.) Sanitary Flange |
| Filter Grade | Standard Milligard® Media |
| 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. |
| 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 | |
|---|---|
| Inlet Connection | Sanitary Flange |
| Outlet Connection | Sanitary Flange |
| Gravimetric Extractables | The extractables level was equal to or less than 25 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 | 4 in. (10 cm) |
| Length | 19.6 cm (7.7 in.) |
| Diameter | 12.5 cm (4.9 in.) |
| Filtration Area | 0.2 m² |
| Inlet to Outlet Width | 19.6 cm (7.7 in.) |
| Device Size | 4 in. |
| Inlet Connection Diameter | 3/4 in. |
| Nominal Pore Size | 0.5 µm |
| Outlet Connection Diameter | 3/4 in. |
| Materials Information | |
|---|---|
| Chemistry | Mixed Cellulose Esters (MCE) |
| Device Material | Polypropylene |
| Seal Material | Silicone (SI) |
| Support Material | Polyester |
| Vent Cap Material | Polypropylene (PP) |
| Packaging Information | |
|---|---|
| Material Size | 3 |
| Material Package | Double Easy-Open bag |
| Specifications | |
|---|---|
| Oxidizable Substances | Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L |
