重要规格表
| Description
|
| Catalogue Number | VPPS201NB1 |
| Description | Viresolve® Pro Magnus 2.1 Shield |
| Product Information
|
| Device Configuration | Magnus 2.1 Shield H |
| 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
|
| Applications
|
| Key Applications |
|
| Physicochemical Information
|
| Maximum Inlet Pressure (psig) | 60 psig |
| Non-Fiber Releasing | This product was manufactured with materials that meet the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6). |
| TOC/Conductivity | After a controlled water flush of 50 L/m², samples exhibited less than 500 ppb TOC per USP <643> and less than 1.3 µS/cm per USP <645>. |
| USP Bacterial Endotoxins | A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. |
| Dimensions
|
| Device Size | 2.1 in. |
| Materials Information
|
| Chemistry |
|
| Toxicological Information
|
| Safety Information according to GHS
|
| Storage and Shipping Information
|
| Packaging Information
|
| Material Size | 1 |
