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  6. 3M™ Zeta Plus™ Encapsulated Filter Capsules with ZB Grade Media

3M™ Zeta Plus™ Encapsulated Filter Capsules with ZB Grade Media

Products
  • Easy-to-use, quick set-up and easy disposal
  • Flexibility for flow rate and batch volume requirements. Same Zeta Plus filter media used in larger diameter cartridges enables linear and predictable scale-up to manufacturing scale
  • Self-Contained Filter Assemblies- Minimises operator contact with process fluid to ensure operator safety
  • Economical, efficient removal of negatively charged contaminants such as bacterial endotoxin, bacteria, DNA and particulates. FDA Drug Master Files (DMF) to assist manufacturers with regulatory submissions
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Overall Diameter (Metric)
Overall_Diameter_Metric
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 Overall Diameter (Metric)
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Specifications
Applications
Bioburden Reduction, Cell Culture Clarification
Brand
Zeta Plus™
End Modification
Luer
Factory Integrity Tested
Cellulose
Filter Material
Cellulose
Filter Type
Depth
Formulation
N/A
Industries
Life Sciences
Maximum Operating Temperature (Celsius)
40 Degree Celsius
MERV Rating
N/A
Overall Diameter (Metric)
66.8 mm
Product Series
ZB
Series
Zeta Plus™ Encapsulated Series
Details

3M™ Zeta Plus™ BC Series are totally disposable capsule depth filters for laboratory, process development, scale-up or small lot production. The Zeta Plus BC Series is a range of completely encapsulated disposable depth filter assemblies, designed for small volume biological, bioprocess and pharmaceutical filtration. Zeta Plus BC units are available in three sizes with a wide range of industry-leading Zeta Plus depth filter media to provide a high degree of application flexibility.

  • Easy-to-use, quick set-up and easy disposal
  • Flexibility for flow rate and batch volume requirements. Same Zeta Plus filter media used in larger diameter cartridges enables linear and predictable scale-up to manufacturing scale
  • Self-Contained Filter Assemblies- Minimises operator contact with process fluid to ensure operator safety
  • Economical, efficient removal of negatively charged contaminants such as bacterial endotoxin, bacteria, DNA and particulates. FDA Drug Master Files (DMF) to assist manufacturers with regulatory submissions