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이전상품 Opticap® XL5 Milligard® Low Protein Binding 1.2 µm 1-1/2 in. TC/TC 다음 상품 Opticap® XL10 Durapore® 0.1 µm 9/16 in. HB/HB

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Opticap® XL5 Milligard® 1.2 µm 1-1/2 in. TC/TC 요약정보 및 구매

판매가격	전화문의
배송비결제	주문시 결제
제조사	Merck
원산지	USA

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Description
Catalogue Number	KW19A05TT1
Trade Name	Opticap®
Description	Opticap® XL5 Milligard® 1.2 µm 1-1/2 in. TC/TC

Product Information
Format	Single Layer
Device Configuration	Capsule
Connections, Inlet/Outlet	38 mm (1-1/2 in.) Sanitary Flange
Filter Grade	Standard Milligard® Media
Housing Material	Polypropylene (PP)
Maximum Differential Pressure, bar (psid)	3.5 bar (50 psid) @ 25 °C
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
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.
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	Milligard®
Sterilization	3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable

Physicochemical Information
Pore Size	1.2 µm
Inlet Connection	Sanitary Flange
Outlet Connection	Sanitary Flange
Gravimetric Extractables	The extractables level was equal to or less than 25 mg per capsule 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.
Maximum Inlet Pressure (psig)	80 psig
Maximum Inlet Temperature	25 °C
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).
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	5 in. (12.5 cm)
Length	21.6 cm (8.5 in.)
Diameter	14.5 cm (5.7 in.)
Filtration Area	0.34 m²
Inlet to Outlet Width	21.6 cm (8.5 in.)
Device Size	5 in.
Inlet Connection Diameter	1-1/2 in.
Nominal Pore Size	1.2 µm
Outlet Connection Diameter	1-1/2 in.

Materials Information
Chemistry	Mixed Cellulose Esters (MCE)
Device Material	Polypropylene
Seal Material	Silicone (SI)
Support Material	Polyester
Vent Cap Material	Polypropylene (PP)

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 ≥2 L

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- 5만원 이하 : 3500원

- 5만원 이상 : 무료

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