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					Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test 
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					Cartridge Nominal Length 4 in. (10 cm) 
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					Catalogue Number KWL6A04HH3 
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					Chemistry Low Protein-Binding Mixed Cellulose Esters (MCE) 
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					Device Configuration Capsule 
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					Device Material Polypropylene 
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					Device Size 4 in. 
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					Diameter 12.5 cm (4.9 in.) 
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					European Pressure Equipment Directive EMD 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. 
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					Filter Grade Low Protein Binding Milligard® Media 
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					Filtration Area 0.2 m² 
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					Format Single Layer 
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					Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. 
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					Gravimetric Extractables The extractables level was equal to or less than 45 mg per capsule after a 2 L flush and 24 hours in water at controlled room temperature. 
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					Housing Material Polypropylene (PP) 
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					Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. 
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					Inlet Connection Hose Barb 
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					Inlet Connection Diameter 9/16 in. 
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					Inlet to Outlet Width 19.6 cm (7.7 in.) 
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					Length 4 in. (10 cm) 
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					Material Package Double Easy-Open bag 
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					Material Size 3 
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					Maximum Differential Pressure, bar (psid) 3.5 bar (50 psid) @ 25 °C 
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					Maximum Inlet Pressure (psig) 80 psig 
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					Maximum Inlet Pressure, bar (psi) 5.5 bar (80 psi) @ 23 °C; 2.75 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C 
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					Maximum Inlet Temperature 25 °C 
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					Media Housing Material 
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					Nominal Pore Size 0.5 µm 
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					Non-Fiber Releasing This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6). 
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					Outlet Connection Hose Barb 
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					Outlet Connection Diameter 9/16 in. 
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					Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L 
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					Pore Size 0.5 µm 
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					Seal Material Silicone (SI) 
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					Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable 
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					Support Material Polyester 
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					Trade Name Opticap® 
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					USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. 
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					Vent Cap Material Polypropylene (PP) 
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					Width 19.6 cm (7.7 in.)