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KZRVA10TT1 Opticap XL10 Viresolve NFR 1-1/2 in. TC/TC

Retrovirus removal

Opticap XL10 Viresolve NFR 1-1/2 in. TC/TC MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
KZRVA10TT1
1  Double Easy-Open bag
Purchase on Sigma-Aldrich

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Replacement Information
Description
Catalogue NumberKZRVA10TT1
Trade Name
  • Viresolve®
DescriptionOpticap XL10 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.
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≤16 mL/min @ 3.45 bar (50 psig) in water
Gravimetric ExtractablesThe extractables level was equal to or less than 35 mg after a 10 minute 1.5 LPM/ft² flush and 24 hours in water at controlled room temperature.
Hold-up Volume175 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
Length33 cm (13 in.)
Filtration Area0.43 m²
Process Volume600 L–1200 L
Device Size10 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 ≥4 L
Global Trade Item Number
Numer katalogowy GTIN
KZRVA10TT1 04053252347665

Documentation

Certificates of Quality

Title
Opticap XL 10 Capsule Viresolve NFR Media C0KB09749
Opticap XL 10 Capsule Viresolve NFR Media C7JA39820
Opticap XL 10 Capsule Viresolve NFR Media C8JA94101
Opticap XL 10 Capsule Viresolve NFR Media C7DA07310
Opticap XL 10 Capsule Viresolve NFR Media C7KA59707
Opticap XL 10 Capsule Viresolve NFR Media C7MA70248
Opticap XL 10 Capsule Viresolve NFR Media C9AA69805
Opticap XL 10 Capsule Viresolve NFR Media - C7NA80251
Opticap XL 10 Capsule Viresolve NFR Media - C8AA20365
Opticap XL 10 Capsule Viresolve NFR Media - C8CA38907
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Data Sheet

Title
Viresolve® NFR Filters

User Guides

Title
Opticap® XL Capsules and Opticap® XLT Capsules