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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

Replacement Information
Description
Catalogue NumberKZRVA2TTT1
Trade Name
  • Viresolve®
DescriptionOpticap XLT20 Viresolve NFR 1-1/2 in. TC/TC
References
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)
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Packaging Information
Material Size1
Material PackageDouble Easy-Open bag
Transport Information
Supplemental Information
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