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이전상품 Durapore® Cartridge Filter 20 in. 0.22 µm Code 7 다음 상품 Durapore Cartridge Filter 20 in. 0.22 µm hydrophobic Code 7

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Durapore® Cartridge Filter 10 in. 0.22 µm Code 7 요약정보 및 구매

판매가격	전화문의
배송비결제	주문시 결제
제조사	Merck
원산지	USA

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Description
Catalogue Number	CVGL71TP3
Trade Name	Durapore®
Description	Durapore® Cartridge Filter 10 in. 0.22 µm 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 10⁷ CFU/cm² using ASTM® F838 methodology.
Wettability	Hydrophilic

Physicochemical Information
Pore Size	0.22 µm
Air Diffusion at 23 °C	≤13.3 mL/min @ 2.75 bar (40 psig) in water
Bubble Point at 23 °C	≥3450 mbar (50 psig) air with water
Flow Rate	50 L/min @ 1.4 bar ΔP
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).
TOC/Conductivity	After sterilization and a controlled water flush of 5.5 L, samples exhibited less than 500 ppb TOC per USP <643> and less than 1.3 µS/cm per USP <645> at 25 °C.
USP Bacterial Endotoxins	A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.

Dimensions
Cartridge Nominal Length	10 in. (25 cm)
Diameter	6.9 cm (2.7 in.)
Filtration Area	0.69 m²
Device Size	10 in.

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

Packaging Information
Material Size	3
Material Package	Double Easy-Open bag

Specifications
Oxidizable Substances	Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L

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