VPMG202NB1

Viresolve^® Pro Device

Parvovirus removal filter, Magnus 2.2 format, filtration area 1.53 m²

• Synonim(y): Viresolve^® Pro Device Magnus 2.2
• Kod UNSPSC: 23151806
• eCl@ss: 32031690

Właściwości

• Materiały: PVDF housing; polyethersulfone membrane; silicone gasket
• Poziom jakości: 400
• linia produktu: EMPROVE^® Filter
• producent / nazwa handlowa: Viresolve^®
• Parametry: 60 psig max. inlet pressure
• dilution: (Large volume processing)
• Wysokość: 9.50 cm (3.74 in.)
• Długość: 34.29 cm (13.50 in.)
• Szerokość: 20.96 cm (8.25 in.)
• Rozmiar urządzenia: 2.2 in.
• powierzchnia filtracyjna: 1.53 m²
• zanieczyszczenia: <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• dopasowywanie: 1.5 in. sanitary TC inlet/outlet fitting(s) (Disposable); 3/4 in. sanitary TC vent fitting for port (disposable)

Opis

Opis ogólny

The Viresolve^® Pro Solution provides a comprehensive, flexible template solution for viral clearance within mAb and recombinant protein bioproduction. This proven viral clearance solution delivers the highest levels of retention assurance and productivity across a broad range of feed stream characteristics.

Viresolve Pro Magnus Devices are typically used for filtration of mid to large scale batch volumes of proteins. The Viresolve^® Pro Device Magnus 2.2 offers a filtration area of 1.53 m² and has a primary use in large-volume processing.

Cechy i korzyści

• Large scale manufacturing
• Two different size formats
• Integrated gaskets
• Units are stackable in the Viresolve^® Pro/Pro+ Magnus Holder (up to 7 units)
• Alignment keys on each unit to minimize errors during installation
• Fully disposable single-use fluid path
• Devices 100% tested with air/water diffusion and Binary Gas Test
• Shield / Shield H 100% aerosol tested

Inne uwagi

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Directions for Use

• Organism Retention: Parvovirus
• Mode of Action: Filtration (size exclusion)
• Application: Protein purification
• Intended Use: Viral clearance
• Instructions for Use: Please see the user guide shipped with this product
• Storage Statement: Store at room temperature
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Uwaga dotycząca przygotowania

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).

Komentarz do analizy

TOC/Conductivity
After a controlled water flush of 50 L/m², samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64>.

Informacje prawne

Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany

VIRESOLVE is a registered trademark of Merck KGaA, Darmstadt, Germany

Oświadczenie o zrzeczeniu się odpowiedzialności

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.

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