重要规格表
| Description
|
| Catalogue Number | KZRVA10TH1 |
| Description | Opticap XL 10 Viresolve NFR TC/HB |
| Product Information
|
| Device Configuration | Capsule |
| Connections, Inlet/Outlet | 38 mm (1-1/2 in.) Sanitary Flange/16 mm (5/8 in.) Hose Barb |
| Connections, Vent/Drain | 1/4 in. Hose Barb with double O-ring Seal |
| 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
|
| Media | Viresolve® NFR |
| Physicochemical Information
|
| Inlet Connection | Sanitary Flange |
| Outlet Connection | Hose Barb |
| Gravimetric Extractables | The extractables level was equal to or less than 35 mg after a 10 minute 1.5 LPM/ft² flush and 24 hours in water at controlled room temperature. |
| Maximum Inlet Pressure (psig) | 80 psig |
| Maximum Inlet Temperature | 25 °C |
| Non-Fiber Releasing | This product was manufactured with a Viresolve® membrane 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
|
| Device Size | 10 in. |
| Inlet Connection Diameter | 1-1/2 in. |
| Outlet Connection Diameter | 9/16 in. |
| Materials Information
|
| Chemistry |
|
| Device Material |
|
| Packaging Information
|
| Material Size | 1 |
