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KZRVA2TTT1 Opticap XLT20 Viresolve NFR 1-1/2 in. TC/TC

Retrovirus removal

Opticap XLT20 Viresolve NFR 1-1/2 in. TC/TC MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
KZRVA2TTT1
1  Double Easy-Open bag
Purchase on Sigma-Aldrich

Overview

Description
Catalogue NumberKZRVA2TTT1
Trade Name
  • Viresolve®
DescriptionOpticap XLT20 Viresolve NFR 1-1/2 in. TC/TC
Product Information
Device ConfigurationCapsule
Connections, Inlet/Outlet38 mm (1-1/2 in.) Sanitary Flange
Connections, Vent/Drain1/4 in. Hose Barb with double O-ring Seal
Maximum Differential Pressure, bar (psid)Forward: 5.5 bar (80 psid). Reverse: 3.4 bar (50 psid)
Maximum Inlet Pressure, bar (psi)5.5 bar (80 psi) @ 23 °C
European Pressure Equipment DirectiveEMD 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.
Good Manufacturing PracticesThese products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
T-line/Gauge PortT-line
Quality LevelMQ400
Applications
ApplicationRetrovirus removal
Key Applications
  • Protein Purification
Biological Information
Bacterial EndotoxinsAqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
MediaViresolve® NFR
SterilizationAfter wetting, may be autoclaved for 3 cycles of up to 60 min at 125 °C, using liquid cycle, slow exhaust.
Physicochemical Information
Inlet ConnectionSanitary Flange
Outlet ConnectionSanitary Flange
Air Diffusion at 23 °C≤32 mL/min @ 3.45 bar (50 psig) in water
Gravimetric ExtractablesThe extractables level was equal to or less than 70 mg after a 10 minute 1.5 LPM/ft² flush and 24 hours in water at controlled room temperature.
Hold-up Volume325 mL
Maximum Inlet Pressure (psig)80 psig
Maximum Inlet Temperature25 °C
Non-Fiber ReleasingThis product was manufactured with a Viresolve® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
USP Bacterial EndotoxinsA sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
Dimensions
Length63.5 cm (25 in.)
Filtration Area0.854 m²
Inlet to Outlet Width15.2 cm (6.0 in.)
Process Volume1200 L–2400 L
Device Size20 in.
Inlet Connection Diameter1-1/2 in.
Outlet Connection Diameter1-1/2 in.
Materials Information
Chemistry
  • Polyethersulfone (PES)
Device Material
  • Polypropylene
Seal MaterialSilicone (SI)
Support MaterialPolypropylene
Vent Cap MaterialPolypropylene (PP)
Packaging Information
Material Size1
Material PackageDouble Easy-Open bag
Specifications
Oxidizable SubstancesWill meet the USP Oxidizable Substances Test requirements after a water flush of ≥8 L
Global Trade Item Number
Catalogue Number GTIN
KZRVA2TTT1 04053252499715