Pegasus™ SV4 Virus Removal Filter Membrane in Minidisc Capsules product photo Primary L

Pegasus™ SV4 Virus Removal Filter Membrane in Minidisc Capsules

Compact, Easily-scalable Capsules for Virus Removal and Small-scale Membrane Qualification Studies

Pegasus SV4 Virus Removal filters combine robust, high viral clearance of parvovirus and larger viruses with high throughput capacity and stable flowrates in both dilute and complex, concentrated biological fluids. Consistent flowrate and throughput performance provide superior control of process costs and maximize virus filtration economy and efficiency.

Pall Minidisc Capsules with Pegasus SV4 Virus Removal Filter Membrane are purpose-designed for small-scale membrane qualification studies such as bacteriophage or prion (TSE agent) clearance, as well as membrane flow rate, capacity and protein transmission studies. They are 100% manufacturing tested and manufactured under a Quality Management System certified to ISO 9001:2008 in order to assure consistent high quality.

 
Features Benefits
Fully disposable capsule with Luer connections Easy handling, ready to use
Pegasus SV4 virus removal filter membrane Robust, high > 4 LRV parvovirus virus clearance
Constant flow and high throughput performance Maximize virus filter process economy as well as efficiency
Identical membrane to larger production scale Pegasus SV4 virus filter cartridges Offers reliable scalability
Individual capsules identified by lot and serial number Easy identification of individual capsules with
complete traceability of manufacturing history
100% manufacturing assembly tested Assurance of consistently high quality
Membrane bacteriophage tested Assurance of consistently high quality
Pre- and post-use installation testable Assurance of consistently high quality at point of use
Low protein-binding High protein recovery
Robust membrane with high viral clearance Flow decay minimized at high virus spike concentrations and with complex or concentrated feeds
 

High Quality Standards

  • Meets the current USP requirements under Section <85> Bacterial Endotoxins Test.

Materials

  • Filter fluid path components have met the specifications under Section <88> Biological Reactivity Tests in vivo listed in the current revision of the United States Pharmacopeia (USP) for Class VI plastics at 121 °C.


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Capsules

List Price
$ 210.00
Description

Compact, Easily-scalable Capsules for Virus Removal and Small-scale Membrane Qualification Studies

Pegasus SV4 Virus Removal filters combine robust, high viral clearance of parvovirus and larger viruses with high throughput capacity and stable flowrates in both dilute and complex, concentrated biological fluids. Consistent flowrate and throughput performance provide superior control of process costs and maximize virus filtration economy and efficiency.

Pall Minidisc Capsules with Pegasus SV4 Virus Removal Filter Membrane are purpose-designed for small-scale membrane qualification studies such as bacteriophage or prion (TSE agent) clearance, as well as membrane flow rate, capacity and protein transmission studies. They are 100% manufacturing tested and manufactured under a Quality Management System certified to ISO 9001:2008 in order to assure consistent high quality.

 
Features Benefits
Fully disposable capsule with Luer connections Easy handling, ready to use
Pegasus SV4 virus removal filter membrane Robust, high > 4 LRV parvovirus virus clearance
Constant flow and high throughput performance Maximize virus filter process economy as well as efficiency
Identical membrane to larger production scale Pegasus SV4 virus filter cartridges Offers reliable scalability
Individual capsules identified by lot and serial number Easy identification of individual capsules with
complete traceability of manufacturing history
100% manufacturing assembly tested Assurance of consistently high quality
Membrane bacteriophage tested Assurance of consistently high quality
Pre- and post-use installation testable Assurance of consistently high quality at point of use
Low protein-binding High protein recovery
Robust membrane with high viral clearance Flow decay minimized at high virus spike concentrations and with complex or concentrated feeds
 

High Quality Standards

  • Meets the current USP requirements under Section <85> Bacterial Endotoxins Test.

Materials

  • Filter fluid path components have met the specifications under Section <88> Biological Reactivity Tests in vivo listed in the current revision of the United States Pharmacopeia (USP) for Class VI plastics at 121 °C.
Specifications

Materials of Construction

 
Item Material
Membrane Hydrophilic modified polyvinylidene fluoride (PVDF)
Support Disc Polypropylene (Non-woven)
O-ring EPDM
Capsule Inlet and Outlet Polycarbonate
 

 
Pore size
20 nm (nominal)
 

Retention Ratings

 
Virus
Bacteriophage PP7 > 4 log TR*†
 
* Claims based on challenge with parvovirus model bacteriophage (bacterial virus) PP7

† > 4 LRV for PP7 bacteriophage per Parenteral Drug Association (PDA) TR 41 rating method for small virus-retentive filters

> 4 LRV typically with mammalian parvoviruses


 
Effective Surface Area
9.6 cm2 (1.49 in.2)
 

 
Operating Parameters1
Maximum Temperature 25°C
Maximum Operating Pressure 3.1 barg (45 psig)
Maximum Differential Pressure 3.1 bard (45 psid)
 
1 Temporary pressures up to 3.4 barg (50 psig) are acceptable, but the target operating and differential pressures should not exceed 3.1 bar (45 psi) to allow for pressure fluctuations during testing.
Ordering Information
 
Part Number  
10MCFSV4 Pall Minidisc Capsules with Pegasus SV4 Virus Removal Filter Membrane*
 
* Three capsules per box


Further Equipment Recommended for Laboratory Testing

 
Part Number Pressure Vessels (disposable)
C3EP1 Novasip™ vessel
 

 
Part Number Accessories (Novasip Vessel)
GFX0290 Adapter 1 in. TC/Male Stäubli connector plug (3 mm) R 14 in.
SLK1TC23H4 TC clamp + silicone gasket
 
Application
Filters - Plasma and High-Fouling mAb
Segment
Viral Clearance