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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
					2 in. (5 cm)
					
				 
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Catalogue Number
					KTGRA02NN3
					
				 
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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
					2 in.
					
				 
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Diameter
					8.4 cm (3.3 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
					0.1 m²
					
				 
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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 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
					NPT
					
				 
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Inlet Connection Diameter
					1/4 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)
					Forward: 5.5 bar (80 psid) @ 25 °C; 1.0 bar (15 psid) @ 80 °C. Reverse: 4.1 bar (60 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; 2.75 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
					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
					NPT
					
				 
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Outlet Connection Diameter
					1/4 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; not in-line steam sterilizable
					
				 
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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
					Hydrophobic