VPMD102NB1 MilliporeViresolve® Pro Modus 1.2 Device
Recommended Products
Overview
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Description | |
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Catalogue Number | VPMD102NB1 |
Trade Name |
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Description | Viresolve® Pro Modus 1.2 Device |
References |
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Product Information | |
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HS Code | 8421 29 90 |
Device Configuration | Modus 1.2 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 |
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Key Applications |
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Biological Information |
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Dimensions | |
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Height | 7.85 cm (3.09 in.) |
Width | 9.22 cm (3.63 in.) |
Length | 18.62 cm (7.33 in.) |
Filtration Area | 0.07 m² |
Device Size | 1.2 in. |
Materials Information | |
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Chemistry |
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Materials of Construction | Membrane: Polyethersulfone (PES); Gaskets: Silicone; Housing: Polyvinylidene fluoride (PVDF) |
Toxicological Information |
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Safety Information according to GHS |
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Safety Information |
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Product Usage Statements |
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Storage and Shipping Information |
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Packaging Information | |
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Material Size | 1 |
Transport Information |
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Supplemental Information |
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Specifications |
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Global Trade Item Number | |
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Catalogue Number | GTIN |
VPMD102NB1 | 04053252450624 |
Documentation
Material Qualification Dossier
Title | Version |
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5.0 |
Quality Management Dossier (Open Access)
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Operational Excellence Dossier
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Certificates of Quality
User Guides
Title |
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Viresolve® Pro Modus and Magnus Devices User Guide |