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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
					2 in. (5 cm)
					
				 
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Catalogue Number
					KWSCA02FF3
					
				 
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Chemistry
					Mixed Cellulose Esters (MCE)
					
				 
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Device Configuration
					Capsule
					
				 
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Device Material
					Polypropylene
					
				 
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Device Size
					2 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
					Standard Milligard® Media
					
				 
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Filtration Area
					0.07 m²
					
				 
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Format
					Double 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 15 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
					3/4 in.
					
				 
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Inlet to Outlet Width
					14.2 cm (5.6 in.)
					
				 
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Length
					2 in. (5 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
					1.2 / 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
					Sanitary Flange
					
				 
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Outlet Connection Diameter
					3/4 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
					1.2 / 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
					14.2 cm (5.6 in.)