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
	KGW6A3THH1	Opticap® XLT30 Polysep® II 1.0/0.5 µm 5/8 in. HB	512	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGW6A3THH1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 5/8 in. Filtration Area 1.38 m² Format Double Layer 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 435 mg per capsule after a 15 L flush and 24 hours in water at controlled room temperature. 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, bar (psid) 3.5 bar (50 psid) @ 25 °C Maximum Inlet Pressure (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Polysep™ II Nominal Pore Size 1.0 / 0.5 µm 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). 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 ≥15 L Pore Size 1.0 / 0.5 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polypropylene Trade Name Opticap® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Width 19.8 cm (7.8 in.)
	KGW6A3THH1	Opticap® XLT30 Polysep® II 1.0/0.5 µm 5/8 in. HB	512	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGW6A3THH1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 5/8 in. Filtration Area 1.38 m² Format Double Layer 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 435 mg per capsule after a 15 L flush and 24 hours in water at controlled room temperature. 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, bar (psid) 3.5 bar (50 psid) @ 25 °C Maximum Inlet Pressure (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Polysep™ II Nominal Pore Size 1.0 / 0.5 µm 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). 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 ≥15 L Pore Size 1.0 / 0.5 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polypropylene Trade Name Opticap® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Width 19.8 cm (7.8 in.)
	KGW6A3TTT1	Opticap® XLT30 Polysep® II 1.0/0.5 µm 1-1/2 in. TC	512	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGW6A3TTT1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 1-1/2 in. Filtration Area 1.38 m² Format Double Layer 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 435 mg per capsule after a 15 L flush and 24 hours in water at controlled room temperature. 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, bar (psid) 3.5 bar (50 psid) @ 25 °C Maximum Inlet Pressure (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Polysep™ II Nominal Pore Size 1.0 / 0.5 µm 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). Outlet Connection Sanitary Flange Outlet Connection Diameter 1-1/2 in. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥15 L Pore Size 1.0 / 0.5 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polypropylene Trade Name Opticap® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Width 15.2 cm (6.0 in.)
	KGW6A3TTT1	Opticap® XLT30 Polysep® II 1.0/0.5 µm 1-1/2 in. TC	512	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGW6A3TTT1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 1-1/2 in. Filtration Area 1.38 m² Format Double Layer 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 435 mg per capsule after a 15 L flush and 24 hours in water at controlled room temperature. 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, bar (psid) 3.5 bar (50 psid) @ 25 °C Maximum Inlet Pressure (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Polysep™ II Nominal Pore Size 1.0 / 0.5 µm 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). Outlet Connection Sanitary Flange Outlet Connection Diameter 1-1/2 in. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥15 L Pore Size 1.0 / 0.5 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polypropylene Trade Name Opticap® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Width 15.2 cm (6.0 in.)
	KGW9A3THH1	Opticap® XLT30 Polysep® II 2.0/1.2 µm 5/8 in. HB	512	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGW9A3THH1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 5/8 in. Filtration Area 1.38 m² Format Double Layer 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 435 mg per capsule after a 15 L flush and 24 hours in water at controlled room temperature. 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, bar (psid) 3.5 bar (50 psid) @ 25 °C Maximum Inlet Pressure (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Polysep™ II Nominal Pore Size 2.0 / 1.2 µm 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). 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 ≥15 L Pore Size 2.0 / 1.2 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polypropylene Trade Name Opticap® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Width 19.8 cm (7.8 in.)
	KGW9A3THH1	Opticap® XLT30 Polysep® II 2.0/1.2 µm 5/8 in. HB	512	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGW9A3THH1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 5/8 in. Filtration Area 1.38 m² Format Double Layer 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 435 mg per capsule after a 15 L flush and 24 hours in water at controlled room temperature. 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, bar (psid) 3.5 bar (50 psid) @ 25 °C Maximum Inlet Pressure (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Polysep™ II Nominal Pore Size 2.0 / 1.2 µm 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). 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 ≥15 L Pore Size 2.0 / 1.2 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polypropylene Trade Name Opticap® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Width 19.8 cm (7.8 in.)
	KGW9A3TTT1	Opticap® XLT30 Polysep® II 2.0/1.2 µm 1-1/2 in. TC	512	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGW9A3TTT1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 1-1/2 in. Filtration Area 1.38 m² Format Double Layer 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 435 mg per capsule after a 15 L flush and 24 hours in water at controlled room temperature. 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, bar (psid) 3.5 bar (50 psid) @ 25 °C Maximum Inlet Pressure (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Polysep™ II Nominal Pore Size 2.0 / 1.2 µm 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). Outlet Connection Sanitary Flange Outlet Connection Diameter 1-1/2 in. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥15 L Pore Size 2.0 / 1.2 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polypropylene Trade Name Opticap® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Width 15.2 cm (6.0 in.)
	KGW9A3TTT1	Opticap® XLT30 Polysep® II 2.0/1.2 µm 1-1/2 in. TC	512	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGW9A3TTT1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 1-1/2 in. Filtration Area 1.38 m² Format Double Layer 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 435 mg per capsule after a 15 L flush and 24 hours in water at controlled room temperature. 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, bar (psid) 3.5 bar (50 psid) @ 25 °C Maximum Inlet Pressure (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Polysep™ II Nominal Pore Size 2.0 / 1.2 µm 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). Outlet Connection Sanitary Flange Outlet Connection Diameter 1-1/2 in. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥15 L Pore Size 2.0 / 1.2 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polypropylene Trade Name Opticap® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP) Width 15.2 cm (6.0 in.)
	KGW9A3ZTT1	Oticap XLT 30 Polysep® II - 30" 2.0/1.2 µm TC/TC 1pk	512	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Nominal Length 30 in. (75 cm) Catalogue Number KGW9A3ZTT1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 1-1/2 in. Format Double Layer 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 435 mg per capsule after a 15 L flush and 24 hours in water at controlled room temperature. 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. Length 30 in. (75 cm) Material Package Double Easy-Open bag Material Size 1 Maximum Differential Pressure, bar (psid) 3.5 bar (50 psid) @ 25 °C Maximum Inlet Pressure (psig) 80 psig 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 Maximum Inlet Temperature 25 °C Media Polysep™ II Nominal Pore Size 2.0 / 1.2 µm 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). Outlet Connection Sanitary Flange Outlet Connection Diameter 1-1/2 in. Pore Size 2.0 / 1.2 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polypropylene Trade Name Opticap® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polypropylene (PP)
	MPGL2GCF3	Sterile Millipak®-200 Filter Unit 0.22 µm 3/4 in. TC/TC	521	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. Catalogue Number MPGL2GCF3 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Gamma Gold Capsule Device Material Polycarbonate Diameter 3/4 in. Filtration Area 1000 cm² Flow Rate 19 L/min @ 2.8 bar ΔP 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 5 mg per sterilized device after a 200 mL flush and 24 hours in water at controlled room temperature. Inlet Connection Sanitary Flange Inlet Connection Diameter 3/4 in. Material Package Blister Material Size 3 Maximum Differential Pressure, bar (psid) Forward: 4.1 bar (60 psid) @ 25 °C; 1.7 bar (25 psid) @ 80 °C; 0.35 bar (5 psid) @ 123 °C; Reverse: 0.7 bar (10 psid) @ 25 °C Maximum Inlet Pressure, bar (psi) 5.2 bar (75 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). Outlet Connection Sanitary Flange Outlet Connection Diameter 3/4 in. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥200 mL Pore Size 0.22 µm Process Volume 100 L Sterility Sterile Sterilization 3 autoclave cycles of 90 min @ 123 °C; not in-line steam sterilizable Support Material Polycarbonate Trade Name Millipak® USP Bacterial Endotoxins A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test. Vent Cap Material Polyvinylidene fluoride (PVDF) Volume 100 L Wettability Hydrophilic

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Analytical Sample Preparation Membrane Filtration Devices

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