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KVGLG04FF3 Opticap® Gamma Compatible XL4 Durapore® 0.22 µm 3/4 in. TC/TC

Opticap® Gamma Compatible XL4 Durapore® 0.22 µm 3/4 in. TC/TC: MSDS (material safety data sheet) o SDS, certificato d’analisi (CoA) e certificato di qualità (CoQ), dossier, brochure e altri documenti disponibili.
KVGLG04FF3
3  Double Easy-Open bag
Purchase on Sigma-Aldrich

Panoramica

Replacement Information
Description
Catalogue NumberKVGLG04FF3
Trade Name
  • Opticap®
DescriptionOpticap® Gamma Compatible XL4 Durapore® 0.22 µm 3/4 in. TC/TC
References
Product Information
Device ConfigurationCapsule
Connections, Inlet/Outlet19 mm (3/4 in.) Sanitary Flange
Connections, Vent/Drain1/4 in. Hose Barb with double O-ring Seal
Housing MaterialPolypropylene (PP)
Maximum Differential Pressure, bar (psid)Forward: 5.5 bar (80 psid) @ 25 °C; 1.0 bar (15 psid) @ 80 °C. Reverse: 2.8 bar (40 psid) @ 25 °C, intermittent
Maximum Inlet Pressure, bar (psi)5.5 bar (80 psi) @ 23 °C; 2.8 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °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
Biological Information
Bacterial EndotoxinsAqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
MediaDurapore®
SterilityNon-sterile, Gamma compatible
Sterilization3 autoclave cycles of 60 min @ 126 °C; capable of 45 kilogray (4.5 Megarad) gamma exposure; not in-line steam sterilizable
Bacterial RetentionSamples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
WettabilityHydrophilic
Physicochemical Information
Pore Size0.22 µm
Inlet ConnectionSanitary Flange
Outlet ConnectionSanitary Flange
Air Diffusion at 23 °C≤4.6 mL/min @ 2.75 bar (40 psig) in water
Bubble Point at 23 °C≥3450 mbar (50 psig) air with water
Indirect Food AdditiveAll component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
Maximum Inlet Pressure (psig)80 psig
Maximum Inlet Temperature25 °C
Non-Fiber ReleasingThis product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
TOC/ConductivityAfter sterilization and a controlled water flush, samples exhibited less than 500 ppb TOC per USP <643> and less than 1.3 µS/cm per USP <645> at 25 ºC.
USP Bacterial EndotoxinsA sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
Dimensions
Cartridge Nominal Length4 in. (10 cm)
Length17.0 cm (6.7 in.)
Diameter6.1 cm (2.4 in.)
Filtration Area0.18 m²
Device Size4 in.
Inlet Connection Diameter3/4 in.
Outlet Connection Diameter3/4 in.
Materials Information
Chemistry
  • Polyvinylidene Fluoride (PVDF)
Device Material
  • Gamma-stable polypropylene
Seal MaterialLead O-ring: Silicone-coated EPDM, Outer O-ring: Silicone
Support MaterialPolyester
Vent Cap MaterialPolypropylene (PP)
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Packaging Information
Material Size3
Material PackageDouble Easy-Open bag
Transport Information
Supplemental Information
Specifications
Oxidizable SubstancesWill meet the USP Oxidizable Substances Test requirements after a water flush of ≥500 mL
Global Trade Item Number
Numero di catalogo GTIN
KVGLG04FF3 04053252374401

Documentation

Material Qualification Dossier

TitoloVersione
3.0

Quality Management Dossier (Open Access)

Title

Operational Excellence Dossier

Title

Certificati di Qualità

Titolo
OPTICAP XL 4 Capsule Durapore Membrane C3BB94694
OPTICAP XL 4 Capsule Durapore Membrane C3JB33898
OPTICAP XL 4 Capsule Durapore Membrane C4KB71894
Opticap XL 4 Capsule Durapore Membrane C7DA92089
Opticap XL 4 Capsule Durapore Membrane C7EA14674
Opticap XL 4 Capsule Durapore Membrane C0CB41374Z
Opticap XL 4 Capsule Durapore Membrane C8BA23066
Opticap XL 4 Capsule Durapore Membrane C0DB61788Z
Opticap XL 4 Capsule Durapore Membrane C1DB07757
Opticap XL 4 Capsule Durapore Membrane C7HA23521
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Informazioni tecniche

Titolo
Establishing Product Specific Bubble Point Specifications For Sterilizing-Grade Filters
Simplified, efficient sizing of sterilizing-grade normal flow filters for buffer solutions

Scheda tecnica

Titolo
Durapore® Family Guide

Manuali d'uso

Titolo
Opticap® XL Capsules and Opticap® XLT Capsules

Prodotti e applicazioni correlate

Linee di prodotti

Filtri sterilizzabili a raggi gamma con membrana Durapore® di grado sterilizzante da 0,1 µm o 0,22 µm

Enhanced process efficiency and cost-effectiveness from reduced cleaning and validation requirements
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Durapore® 0.1 µm and 0.22 µm Capsule Filters

0.1 µm and 0.22 µm hydrophilic polyvinylidene fluoride (PVDF) membranes for sterile liquid filtration
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Prodotti correlati per: Brand Facete

Opticap®

Categorie

Biopharmaceutical Manufacturing > Downstream Processing > Sterile Filtration > Sterile Liquid > Durapore