VPMD101NB1
Viresolve® Pro Device
Parvovirus removal filter, Modus 1.1 format, filtration area 0.017 m²
Synonym(s):
Viresolve® Pro Device Modus 1.1
About This Item
Recommended Products
material
PVDF housing
polyethersulfone membrane
silicone gasket
Quality Level
product line
EMPROVE® Filter
manufacturer/tradename
Viresolve®
parameter
60 psig max. inlet pressure
dilution
(Scale studies/Pilot)
H
5.92 cm (2.33 in.)
L
18.62 cm (7.33 in.)
W
9.22 cm (3.63 in.)
device size
1.1 in.
filtration area
0.017 m2
impurities
<0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
fitting
1/4 in. integrated vent hose barb (with double O-ring seal)
3/4 in. sanitary TC inlet/outlet fitting(s)
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General description
Viresolve Pro Modus devices are typically used for filtration of pilot to mid-scale batch volumes of proteins. The Viresolve® Pro Device Modus 1.1 offers a filtration area of 0.017 m2 and has a primary use in pilot/small-volume processing.
Other Notes
- 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.
Preparation Note
Analysis Note
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>.
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Articles
This page provides an overview of USP <87>, <88>, and <1031>, compares bioreactivity testing, and describes the transition of our organization towards in vitro test methods.
This page provides an overview of USP <87>, <88>, and <1031>, compares bioreactivity testing, and describes the transition of our organization towards in vitro test methods.
This page provides an overview of USP <87>, <88>, and <1031>, compares bioreactivity testing, and describes the transition of our organization towards in vitro test methods.
This page provides an overview of USP <87>, <88>, and <1031>, compares bioreactivity testing, and describes the transition of our organization towards in vitro test methods.
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