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
	CV0671TP3	Durapore® Multimedia Cartridge Filter 10 in. 0.5+0.22 µm Code 7	1303	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤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 CV0671TP3 Chemistry Mixed Cellulose Esters (MCE)Polyvinylidene Fluoride (PVDF) Device Configuration Cartridge Device Material Polypropylene Device Size 10 in. Diameter 6.9 cm (2.7 in.) Filtration Area 0.69 m² 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 45 mg per 10-inch cartridge 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. Length 10 in. (25 cm) Material Package Double Easy-Open bag Material Size 3 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, intermittent 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, Intermittent Media Multimedia 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). Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥5 L Pore Size 0.5 / 0.22 µm Seal Material Silicone (SI) Sterility Other Sterilization 6 autoclave or SIP cycles of 30 min @ 123 °C Support Material Polypropylene 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
	KHVEA3TBB1	Opticap® Autoclavable XLT 30 Millipore Express® SHR with Prefilter 0.5/0.1 µm 1 in. HB/HB	1304	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 KHVEA3TBB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.48 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 @ 23 °C; 5.5 bar (80 psi) @ 23 °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) Sterilization 3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable Support Material Polypropylene 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.)
	KHVEA3TBB1	Opticap® Autoclavable XLT 30 Millipore Express® SHR with Prefilter 0.5/0.1 µm 1 in. HB/HB	1304	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 KHVEA3TBB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.48 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 @ 23 °C; 5.5 bar (80 psi) @ 23 °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) Sterilization 3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable Support Material Polypropylene 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.)
	KHVEA3TTB1	Opticap® Autoclavable XLT 30 Millipore Express® SHR with Prefilter 0.5/0.1 µm 1-1/2 in. TC-1 in. HB	1304	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 KHVEA3TTB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.48 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 @ 23 °C; 5.5 bar (80 psi) @ 23 °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) Sterilization 3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable Support Material Polypropylene 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.)
	KHVEA3TTB1	Opticap® Autoclavable XLT 30 Millipore Express® SHR with Prefilter 0.5/0.1 µm 1-1/2 in. TC-1 in. HB	1304	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 KHVEA3TTB1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.48 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 @ 23 °C; 5.5 bar (80 psi) @ 23 °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) Sterilization 3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable Support Material Polypropylene 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.)
	KHVEA3TTH1	Opticap® Autoclavable XLT 30 Millipore Express® SHR with Prefilter 0.5/0.1 µm 1-1/2 in. TC-5/8 in. HB	1304	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 KHVEA3TTH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.48 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 @ 23 °C; 5.5 bar (80 psi) @ 23 °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) Sterilization 3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable Support Material Polypropylene 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.)
	KHVEA3TTH1	Opticap® Autoclavable XLT 30 Millipore Express® SHR with Prefilter 0.5/0.1 µm 1-1/2 in. TC-5/8 in. HB	1304	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 KHVEA3TTH1 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Polypropylene/Polysulfone Device Size 30 in. Diameter 10.7 cm (4.2 in.) Filtration Area 1.48 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 @ 23 °C; 5.5 bar (80 psi) @ 23 °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) Sterilization 3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable Support Material Polypropylene 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.)
	XX80LFL25	Labscale System 1/8" Tubing Kit	1324	Add to Cart
Catalogue Number XX80LFL25 Diameter 3.18 mm Length 7.62 m (25 ft.) Material Size 1 Trade Name Pellicon®
	CVHL52PP3	Durapore® Cartridge Filter without prefilter 20 in. 0.45 µm Code 5	1325	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Code Code 5 (2-222) O-rings and spear Cartridge Nominal Length 20 in. (50 cm) Catalogue Number CVHL52PP3 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cartridge Device Material Polypropylene Device Size 20 in. Diameter 6.9 cm (2.7 in.) Filtration Area 1.38 m² 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 20 mg per 10-inch cartridge 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. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food. Length 20 in. (50 cm) Material Package Double Easy-Open bag Material Size 3 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 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). Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L Pore Size 0.45 µm Seal Material Silicone (SI) Sterility Other Sterilization 30 SIP cycles of 30 min @ 135 °C; 30 autoclave cycles of 60 min @ 126 °C Support Material Polypropylene 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
	CVHL52PP3	Durapore® Cartridge Filter without prefilter 20 in. 0.45 µm Code 5	1325	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Code Code 5 (2-222) O-rings and spear Cartridge Nominal Length 20 in. (50 cm) Catalogue Number CVHL52PP3 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cartridge Device Material Polypropylene Device Size 20 in. Diameter 6.9 cm (2.7 in.) Filtration Area 1.38 m² 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 20 mg per 10-inch cartridge 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. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food. Length 20 in. (50 cm) Material Package Double Easy-Open bag Material Size 3 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 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). Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L Pore Size 0.45 µm Seal Material Silicone (SI) Sterility Other Sterilization 30 SIP cycles of 30 min @ 135 °C; 30 autoclave cycles of 60 min @ 126 °C Support Material Polypropylene 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

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