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Merck默克Millipore密理博0.22um除菌濾芯CVGL75S01

產(chǎn)品簡介：Merck默克Millipore密理博0.22um除菌濾芯CVGL75S01，Durapore Cartridge Filter 5 in. 0.22um Code 7。

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Merck默克Millipore密理博0.22um除菌濾芯CVGL75S01

Description
Catalogue Number	CVGL75S01
Trade Name	Durapore
Description	Durapore Cartridge Filter 5 in. 0.22um Code 7

Product Information
Device Configuration	Cartridge
Maximum Differential Pressure, bar (psid)	Forward: 5.5 bar (80 psid) @ 25 °C; 1.7 bar (25 psid) @ 80 °C; 0.35 bar (5 psid) @ 135 °C. Reverse: 3.5 bar (50 psid) @ 25 °C
Maximum Inlet Pressure, bar (psi)	Forward - 5.5 bar (80 psi) @ 25 °C; 1.7 bar (25 psi) @ 80 °C; 0.35 bar (5 psi) @ 135 °C; Reverse - 3.5 bar (50 psi) @ 25 °C
Cartridge Code	Code 7 (2-226) O-rings w/locking-tabs
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?
Sterility	Other
Sterilization	30 SIP cycles of 30 min @ 135 °C; 30 autoclave cycles of 60 min @ 126 °C
Bacterial Retention	Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10? CFU/cm2 using ASTM? F838 methodology.
Wettability	Hydrophilic

Physicochemical Information
Pore Size	0.22 μm
Air Diffusion at 23 °C	≤6.6 mL/min @ 2.75 bar (40 psig) in water
Bubble Point at 23 °C	≥3450 mbar (50 psig) air with water
Flow Rate	25 L/min @ 1.4 bar ΔP
Gravimetric Extractables	The extractables level was equal to or less than 20 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
Indirect Food Additive	All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food.
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.

Materials Information
Chemistry	Polyvinylidene Fluoride (PVDF)
Device Material	Polypropylene
Seal Material	Silicone (SI)
Support Material	Polypropylene

Packaging Information
Material Size	1
Material Package	Double Easy-Open bag

Specifications
Oxidizable Substances	Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥500 mL

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