millipore,密理博,LAGB04TP6,Optiseal Durapore Cartridge Filter 0.22 µm hydrophobic

Description
Catalogue Number	LAGB04TP6
Trade Name	Optiseal^®
Description	Optiseal^® Durapore^® Cartridge Filter 0.22 µm hydrophobic

Product Information
Device Configuration	Cartridge
Maximum Differential Pressure, bar (psid)	Forward: 5.5 bar (80 psid) @ 25 °C; 3.5 bar (50 psid) @ 80 °C; 0.35 bar (5 psid) @ 121 °C. Reverse: 3.5 bar (50 psid) @ 25 °C KEEP
Maximum Inlet Pressure, bar (psi)	Forward - 5.5 bar (80 psi) @ 25 °C; 3.5 bar (50 psi) @ 80 °C; 0.35 bar (5 psi) @ 135 °C; Reverse - 3.5 bar (50 psi) @ 25 °C
Cartridge Code	Not Applicable
Good Manufacturing Practices	These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Quality Level	MQ400

Biological Information
Bacterial Endotoxins	Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Media	Durapore^®
Sterilization	30 SIP cycles of 30 min @ 135 °C; 10 autoclave cycles of 30 min @ 126 °C
Bacterial Retention	Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM^® F838 methodology.
Wettability	Hydrophobic

Physicochemical Information
Pore Size	0.22 µm
Bubble Point at 23 °C	≥1240 mbar (18 psig) nitrogen with 60/40 % IPA/water
Gravimetric Extractables	The extractables level was equal to or less than 10 mg per 4-inch cartridge after 24 hours in a 70/30% IPA/water mixture at controlled room temperature.
Nitrogen Diffusion at 23 °C	≤2 mL/min @ 1.0 bar (15 psig) in 60/40 % IPA/water
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).
USP Bacterial Endotoxins	A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.