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					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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					Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. 
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					Cartridge Nominal Length 10 in. (25 cm) 
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					Catalogue Number KVVLG1ZTH1 
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					Chemistry Polyvinylidene Fluoride (PVDF) 
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					Device Configuration Capsule 
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					Device Material Gamma-stable polypropylene 
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					Device Size 10 in. 
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					Diameter 1-1/2 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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					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 25 mg per capsule after 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 Sanitary Flange 
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					Inlet Connection Diameter 1-1/2 in. 
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					Length 10 in. (25 cm) 
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					Material Package Double Easy-Open bag 
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					Material Size 1 
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					Maximum Differential Pressure, bar (psid) Forward: 5.5 bar (80 psid) @ 25 °C; 1.7 bar (25 psid) @ 80 °C. Reverse: 2.8 bar (40 psid) @ 25 °C, intermittent 
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					Maximum Inlet Pressure (psig) 80 psig 
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					Maximum Inlet Pressure, bar (psi) 5.5 bar (80 psi) @ 25 °C; 2.8 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 Durapore® 
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					Non-Fiber Releasing This 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). 
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					Outlet Connection Hose Barb 
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					Outlet Connection Diameter 5/8 in. 
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					Pore Size 0.1 µm 
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					Seal Material Silicone (SI) 
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					Sterility Gamma 
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					Sterilization 3 autoclave cycles of 60 min @ 126 °C; capable of 45 kilogray (4.5 Megarad) gamma exposure; 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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					Wettability Hydrophilic