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Merck

VPPS201NB1

Millipore

Viresolve Pro Magnus 2.1 护罩

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

别名:

Viresolve® Pro Shield Magnus 2.1

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About This Item

分類程式碼代碼:
23151806
eCl@ss:
32031690

材料

polyethersulfone

品質等級

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)

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.

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