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					Bacterial Endotoxins Aqueous extraction contains <0.25 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 5 in. (13 cm) 
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					Catalogue Number KTGRA05FF1 
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					Chemistry Polytetrafluoroethylene (PTFE) 
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					Device Configuration Capsule 
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					Device Material Polypropylene 
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					Device Size 5 in. 
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					Diameter 10.7 cm (4.2 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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					Filtration Area 0.32 m² 
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					Gravimetric Extractables The extractables level was equal to or less than 28 mg per 10-inch cartridge after 24 hours in a 70/30% IPA/water mixture at controlled room temperature. 
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					Housing Material Polypropylene (PP) 
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					Inlet Connection Sanitary Flange 
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					Inlet Connection Diameter 3/4 in. 
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					Inlet to Outlet Width 21.0 cm (8.3 in.) 
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					Length 5 in. (13 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; 1.0 bar (15 psid) @ 80 °C. Reverse: 4.1 bar (60 psid), intermittent 
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					Maximum Inlet Pressure (psig) 80 psig 
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					Maximum Inlet Pressure, bar (psi) Forward - 5.5 bar (80 psi) @ 25 °C; 2.8 bar (40 psi) @ 60 °C;  1.0 bar (15 psi) @ 80 °C; Reverse - 4.1 bar (60 psi), Intermittent 
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					Maximum Inlet Temperature 25 °C 
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					Media Aervent® 
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					Non-Fiber Releasing This product was manufactured with a PTFE 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 Sanitary Flange 
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					Outlet Connection Diameter 3/4 in. 
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					Pore Size 0.2 µm 
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					Seal Material Silicone (SI) 
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					Sterilization 30 autoclave cycles of 30 min @ 135 °C 
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					Support Material Polypropylene 
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					Trade Name Aervent® 
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					USP Bacterial Endotoxins Aqueous extraction contains <0.25 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 Hydrophobic 
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					Width 21.0 cm (8.3 in.)