KHVEG2TBB1 Opticap Gamma Compatible XLT 20 Millipore Express SHR with prefilter 0 5 0 1 m 1 in HB HB 密理博 millipore

发布时间:2017-07-05

KHVEG2TBB1 | Opticap® Gamma Compatible XLT 20 Millipore Express® SHR with prefilter 0.5/0.1 µm 1 in. HB/HB是由上海肯强供应,产品价格优惠,欢迎致电我公司。 手机: QQ:935581225 邮箱:935581225@qq.com

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KHVEG2TBB1 | Opticap® Gamma Compatible XLT 20 Millipore Express® SHR with prefilter 0.5/0.1 µm 1 in. HB/HB

重要规格表

Deion
Catalogue Number KHVEG2TBB1
Trade Name Millipore Express®
Deion Opticap® Gamma Compatible XLT 20 Millipore Express® SHR with prefilter 0.5/0.1 µm 1 in. HB/HB
Product Information
Device Configuration Capsule
Connections, Inlet/Outlet 25 mm (1 in.) Hose Barb
Connections, Vent/Drain 1/4 in. Hose Barb with double O-ring Seal
Housing Material Polypropylene (PP)
Maximum Differential Pressure, bar (psid) Forward: 6.9 bar (100 psid) intermittent @ 25 °C; 5.5 bar (80 psid) @ 25 °C; 1.0 bar (15 psid) @ 80 °C. Reverse: 2.1 bar (30 psid) @ 25 °C, intermittent
Maximum Inlet Pressure, bar (psi) 6.9 bar (100 psi) intermittent @ 25 °C; 5.5 bar (80 psi) @ 25 °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.
T-line/Gauge Port T-line
Biological Information
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Media Millipore Express® SHR w/Prefilter
Sterility Gamma
Sterilization Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
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 0.5 / 0.1 µm
Inlet Connection Hose Barb
Outlet Connection Hose Barb
Air Diffusion at 23 °C ≤60.8 mL/min @ 3.45 bar (50 psig) in water
Bubble Point at 23 °C ≥2586 mbar (37.5 psig) nitrogen with 70/30 % IPA/water
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 Differential Pressure 80 psi (5.5 bar) continuous 100 psi (6.9 bar) intermittent
Maximum Inlet Temperature 25 °C
Non-Fiber Releasing This product was manufactured with a Millipore Express® 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 40 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 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
Dimensions
Cartridge Nominal Length 20 in. (50 cm)
Length 62.5 cm (24.6 in.)
Diameter 19.8 cm (7.8 in.)
Filtration Area 1.08 m²
Inlet to Outlet Width 19.8 cm (7.8 in.)
Device Size 20 in.
Inlet Connection Diameter 1 in.
Outlet Connection Diameter 1 in.
Materials Information
Chemistry Polyethersulfone (PES)
Device Material Gamma stable polypropylene/Polysulfone
Seal Material Silicone (SI)
Support Material Polyester
Vent Cap Material Gamma stable 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 ≥4 L
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