MD0SP027H1
Millistak+® HC Pro Pod Depth Filter
D0SP, filtration area 0.027 m2, hydrophilic
Synonym(s):
Millistak+ HC Pro Pod Depth Filter, D0SP media series, 0.027 m 2 surface area, 1/4 in. Hose Barb connection
About This Item
material
acrylic
polypropylene
silica filter aid
Quality Level
description
Primary clarification directly out of the bioreactor
feature
hydrophilic
manufacturer/tradename
Millistak+®
parameter
2.1 bar max. differential pressure (30 psid) at 25 °C (Forward)
30 psid max. differential pressure (2.1 bar) at 37 °C (Reverse)
30 psid max. differential pressure (2.1 bar) at 4 °C (Forward)
31 psid max. inlet pressure (2.1 bar) at 25 °C
H
140 mm
5.5 in. (14 cm)
L
8.6 in. (22 cm)
filtration area
0.027 m2
impurities
<0.25 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
input
sample type liquid
conductivity
3.64-10.5 μS/cm at 25 °C (product water)
filter grade
D0SP
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General description
Application
Features and Benefits
- Reduce TOC extractables and pre-use flush volume requirements by 50%
- No beta glucans to interfere with limulous amoebocyte lysate (LAL) testing for bacterial endotoxins
Lot to lot consistency for successful development and implementation of robust clarification processes
Depth filter media formulation & design
- Provide as much as two times the filtration capacity with equivalent filter retention properties over commercial DE-based benchmarks
- Improved HCP impurity clearance
Disposable Pod device
- Flexible, modular format offers scalability from 5 to 12,000 liters or more
- Robust device format; easy to use and set up
Specifications
Preparation Note
1 autoclave cycle of 60 min @ 123 ºC, filtration performance may be impacted. Recommended for post use contamination only.
Analysis Note
Legal Information
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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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