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
	CLVL01TP3	Durapore® 0.1 µm High Area Cartridge 10 in. Code 0	1459	Add to Cart
Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 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 Code Code 0 (2-222) O-rings Cartridge Nominal Length 10 in. (25 cm) Catalogue Number CLVL01TP3 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cartridge Device Size 10 in. Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Gravimetric Extractables The extractables level was equal to or less than 30 mg per 10-inch cartridge after a 1.5 L flush and 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. Length 10 in. (25 cm) Material Size 3 Media Durapore® 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). Pore Size 0.1 µm Sterility Other Trade Name Durapore® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Wettability Hydrophilic
	CLVL71TP3	Durapore® 0.1 µm High Area Cartridge 10 in. Code 7	1459	Add to Cart
Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 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 Code Code 7 (2-226) O-rings w/locking-tabs Cartridge Nominal Length 10 in. (25 cm) Catalogue Number CLVL71TP3 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cartridge Device Size 10 in. Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. Gravimetric Extractables The extractables level was equal to or less than 30 mg per 10-inch cartridge after a 1.5 L flush and 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. Length 10 in. (25 cm) Material Size 3 Media Durapore® 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). Pore Size 0.1 µm Sterility Other Trade Name Durapore® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Wettability Hydrophilic
	KHVES3TBB1	Opticap® Sterile XLT 30 Millipore Express® SHR with prefilter 0.5/0.1 µm 1 in. HB/HB	1462	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 KHVES3TBB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 19.8 cm (7.8 in.) Filtration Area 1.62 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® SHR w/Prefilter 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. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥6 L Pore Size 0.5 / 0.1 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 Gamma stable polypropylene (PP) Wettability Hydrophilic Width 19.8 cm (7.8 in.)
	KHVES3TBB1	Opticap® Sterile XLT 30 Millipore Express® SHR with prefilter 0.5/0.1 µm 1 in. HB/HB	1462	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 KHVES3TBB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 19.8 cm (7.8 in.) Filtration Area 1.62 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® SHR w/Prefilter 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. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥6 L Pore Size 0.5 / 0.1 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 Gamma stable polypropylene (PP) Wettability Hydrophilic Width 19.8 cm (7.8 in.)
	KHVES3THH1	Opticap® Sterile XLT 30 Millipore Express® SHR with prefilter 0.5/0.1 µm 5/8 in. HB	1462	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 KHVES3THH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 19.8 cm (7.8 in.) Filtration Area 1.62 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® SHR w/Prefilter 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 ≥6 L Pore Size 0.5 / 0.1 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 Gamma stable polypropylene (PP) Wettability Hydrophilic Width 19.8 cm (7.8 in.)
	KHVES3THH1	Opticap® Sterile XLT 30 Millipore Express® SHR with prefilter 0.5/0.1 µm 5/8 in. HB	1462	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 KHVES3THH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 19.8 cm (7.8 in.) Filtration Area 1.62 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® SHR w/Prefilter 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 ≥6 L Pore Size 0.5 / 0.1 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 Gamma stable polypropylene (PP) Wettability Hydrophilic Width 19.8 cm (7.8 in.)
	KHVES3TTB1	Opticap® Sterile XLT 30 Millipore Express® SHR with prefilter 0.5/0.1 µm 1-1/2 in. TC-1 in. HB	1462	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 KHVES3TTB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 19.8 cm (7.8 in.) Filtration Area 1.62 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® SHR w/Prefilter 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. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥6 L Pore Size 0.5 / 0.1 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 Gamma stable polypropylene (PP) Wettability Hydrophilic Width 17.5 cm (6.9 in.)
	KHVES3TTB1	Opticap® Sterile XLT 30 Millipore Express® SHR with prefilter 0.5/0.1 µm 1-1/2 in. TC-1 in. HB	1462	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 KHVES3TTB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 19.8 cm (7.8 in.) Filtration Area 1.62 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® SHR w/Prefilter 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. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥6 L Pore Size 0.5 / 0.1 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 Gamma stable polypropylene (PP) Wettability Hydrophilic Width 17.5 cm (6.9 in.)
	KHVES3TTH1	Opticap® Sterile XLT 30 Millipore Express® SHR with prefilter 0.5/0.1 µm 1-1/2 in. TC-5/8 in. HB	1462	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 KHVES3TTH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 19.8 cm (7.8 in.) Filtration Area 1.62 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® SHR w/Prefilter 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 ≥6 L Pore Size 0.5 / 0.1 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 Gamma stable polypropylene (PP) Wettability Hydrophilic Width 17.5 cm (6.9 in.)
	KHVES3TTH1	Opticap® Sterile XLT 30 Millipore Express® SHR with prefilter 0.5/0.1 µm 1-1/2 in. TC-5/8 in. HB	1462	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 KHVES3TTH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Device Size 30 in. Diameter 19.8 cm (7.8 in.) Filtration Area 1.62 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® SHR w/Prefilter 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 ≥6 L Pore Size 0.5 / 0.1 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 Gamma stable polypropylene (PP) Wettability Hydrophilic Width 17.5 cm (6.9 in.)

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Analytical Sample Preparation Membrane Filtration Devices

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