重要规格表
| Description | |
|---|---|
| Catalogue Number | VPMD101NB1 |
| Trade Name |
|
| Description | Viresolve® Pro Modus 1.1 Device |
| Product Information | |
|---|---|
| Device Configuration | Modus 1.1 Device |
| Connections, Inlet/Outlet | Inlet/outlet: 3/4" sanitary TC fittings |
| Connections, Vent/Drain | Integrated vent: 1/4" 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 |
| 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 | |
|---|---|
| Height | 5.92 cm (2.33 in.) |
| Width | 9.22 cm (3.63 in.) |
| Length | 18.62 cm (7.33 in.) |
| Filtration Area | 0.017 m² |
| Device Size | 1.1 in. |
| Materials Information | |
|---|---|
| Chemistry |
|
| Materials of Construction | Membrane: Polyethersulfone (PES); Gaskets: Silicone; Housing: Polyvinylidene fluoride (PVDF) |
| Packaging Information | |
|---|---|
| Material Size | 1 |