Merck - Filters and Filtration - Chromatography - Lab supplies

We have developed a unique portfolio of consumables, each adapted to the different feed water quality requirements and to your various applications. To maintain your water system’s performance, it’s critical to replace your purification cartridges on time and with genuine ISO 9001-certified parts.

Catalog No.		Product	Net Price
	KGEPG3TTH1	Opticap® XLT 30 Millipore Express® SHF Gamma Compatible 0.2 µm 1-1/2 in. TC-5/8 in. HB	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPG3TTH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Sanitary Flange Inlet Connection Diameter 1-1/2 in. Inlet to Outlet Width 17.5 cm (6.9 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Hose Barb Outlet Connection Diameter 5/8 in. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Gamma Sterilization Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 17.5 cm (6.9 in.)
	KGEPS3TBB1	Opticap® XLT 30 Millipore Express® SHF Sterile 0.2 µm 1 in. HB/HB	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPS3TBB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Hose Barb Inlet Connection Diameter 1 in. Inlet to Outlet Width 19.8 cm (7.8 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Hose Barb Outlet Connection Diameter 1 in. Overview Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Sterile Sterilization 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 19.8 cm (7.8 in.)
	KGEPS3TBB1	Opticap® XLT 30 Millipore Express® SHF Sterile 0.2 µm 1 in. HB/HB	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPS3TBB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Hose Barb Inlet Connection Diameter 1 in. Inlet to Outlet Width 19.8 cm (7.8 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Hose Barb Outlet Connection Diameter 1 in. Overview Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Sterile Sterilization 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 19.8 cm (7.8 in.)
	KGEPS3THH1	Opticap® XLT 30 Millipore Express® SHF Sterile 0.2 µm 5/8 in. HB	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPS3THH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Hose Barb Inlet Connection Diameter 5/8 in. Inlet to Outlet Width 19.8 cm (7.8 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Hose Barb Outlet Connection Diameter 5/8 in. Overview Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Sterile Sterilization 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 19.8 cm (7.8 in.)
	KGEPS3THH1	Opticap® XLT 30 Millipore Express® SHF Sterile 0.2 µm 5/8 in. HB	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPS3THH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Hose Barb Inlet Connection Diameter 5/8 in. Inlet to Outlet Width 19.8 cm (7.8 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Hose Barb Outlet Connection Diameter 5/8 in. Overview Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Sterile Sterilization 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 19.8 cm (7.8 in.)
	KGEPS3TTB1	Opticap® XLT 30 Millipore Express® SHF Sterile 0.2 µm 1-1/2 in. TC-1 in. HB	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPS3TTB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Sanitary Flange Inlet Connection Diameter 1-1/2 in. Inlet to Outlet Width 17.5 cm (6.9 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Hose Barb Outlet Connection Diameter 1 in. Overview Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Sterile Sterilization 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 17.5 cm (6.9 in.)
	KGEPS3TTB1	Opticap® XLT 30 Millipore Express® SHF Sterile 0.2 µm 1-1/2 in. TC-1 in. HB	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPS3TTB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Sanitary Flange Inlet Connection Diameter 1-1/2 in. Inlet to Outlet Width 17.5 cm (6.9 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Hose Barb Outlet Connection Diameter 1 in. Overview Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Sterile Sterilization 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 17.5 cm (6.9 in.)
	KGEPS3TTH1	Opticap® XLT 30 Millipore Express® SHF Sterile 0.2 µm 1-1/2 in. TC-5/8 in. HB	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPS3TTH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Sanitary Flange Inlet Connection Diameter 1-1/2 in. Inlet to Outlet Width 17.5 cm (6.9 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Hose Barb Outlet Connection Diameter 5/8 in. Overview Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Sterile Sterilization 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 17.5 cm (6.9 in.)
	KGEPS3TTH1	Opticap® XLT 30 Millipore Express® SHF Sterile 0.2 µm 1-1/2 in. TC-5/8 in. HB	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPS3TTH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Sanitary Flange Inlet Connection Diameter 1-1/2 in. Inlet to Outlet Width 17.5 cm (6.9 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Hose Barb Outlet Connection Diameter 5/8 in. Overview Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Sterile Sterilization 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 17.5 cm (6.9 in.)
	KGEPS3TTT1	Opticap® XLT 30 Millipore Express® SHF Sterile 0.2 µm 1-1/2 in. TC	991	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Bacterial Retention Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology. Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGEPS3TTT1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.71 m² Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Housing Material Polypropylene (PP) Indirect Food Additive All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. Inlet Connection Sanitary Flange Inlet Connection Diameter 1-1/2 in. Inlet to Outlet Width 15.2 cm (6.0 in.) Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure 80 psi (5.5 bar) continuous100 psi (6.9 bar) intermittent 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 (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Millipore Express® SHF 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). Outlet Connection Sanitary Flange Outlet Connection Diameter 1-1/2 in. Overview Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4.5 L Pore Size 0.2 µm Seal Material Silicone (SI) Sterility Sterile Sterilization 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyester Trade Name Millipore Express® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Wettability Hydrophilic Width 15.2 cm (6.0 in.)

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Analytical Sample Preparation Membrane Filtration Devices

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