VPPS201NB1

Viresolve Pro Magnus 2.1 护罩

Virus prefilter, Viresolve^® Pro Shield, Magnus 2.1 format, filtration area 0.51 m²

• 同義詞: Viresolve^® Pro Shield Magnus 2.1
• 分類程式碼代碼: 23151806
• eCl@ss: 32031690

屬性

• 材料: polyethersulfone
• 品質等級: 400
• 產品線: EMPROVE^® Filter
• 參數: 60 psig max. inlet pressure
• dilution: (Large volume processing)
• 設備尺寸: 2.1 in.
• 雜質: <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

描述

一般說明

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 Shield Magnus 2.1 offers a filtration area of 0.51 m² and has a primary use in large-volume processing.

特點和優勢

• 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

其他說明

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

準備報告

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).

分析報告

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>.

法律資訊

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

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

免責聲明

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.