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
	KGW1A3TTT1	Opticap® XLT30 Polysep® II 1.0/0.2/0.1 µm 1-1/2 in. TC	511	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 KGW1A3TTT1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 1-1/2 in. Filtration Area 1.26 m² Format Triple 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 / 0.2 / 0.1 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 / 0.2 / 0.1 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.)
	KGW1A3TTT1	Opticap® XLT30 Polysep® II 1.0/0.2/0.1 µm 1-1/2 in. TC	511	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 KGW1A3TTT1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 1-1/2 in. Filtration Area 1.26 m² Format Triple 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 / 0.2 / 0.1 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 / 0.2 / 0.1 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.)
	MP0DCR0D05	Clamp Rod for Pilot Holder w/Expansion Kit	511	Add to Cart
Catalogue Number MP0DCR0D05 Material Size 1
	MP0DCR0D05	Clamp Rod for Pilot Holder w/Expansion Kit	511	Add to Cart
Catalogue Number MP0DCR0D05 Material Size 1
	KGW2A3TTT1	Opticap® XLT30 Polysep® II 1.0/1.2 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 KGW2A3TTT1 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 / 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 1.0 / 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.)
	KGW2A3TTT1	Opticap® XLT30 Polysep® II 1.0/1.2 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 KGW2A3TTT1 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 / 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 1.0 / 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.)
	KGW3A3THH1	Opticap® XLT30 Polysep® II 1.0/0.2 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 KGW3A3THH1 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 / 0.2 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 1.0 / 0.2 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.)
	KGW3A3THH1	Opticap® XLT30 Polysep® II 1.0/0.2 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 KGW3A3THH1 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 / 0.2 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 1.0 / 0.2 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.)
	KGW3A3TTT1	Opticap® XLT30 Polysep® II 1.0/0.2 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 KGW3A3TTT1 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 / 0.2 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 1.0 / 0.2 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.)
	KGW3A3TTT1	Opticap® XLT30 Polysep® II 1.0/0.2 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 KGW3A3TTT1 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 / 0.2 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 1.0 / 0.2 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.)

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Analytical Sample Preparation Membrane Filtration Devices

Trust Merck membrane filtration devices for the collection and preparation of samples, mobile phases, and buffers to obtain the highest quality results from downstream analysis.

Whether you need to collect, separate, or remove contaminants from air or fluid samples prior to downstream analysis, our broad selection of syringe filters, membranes, filter holders and related filtration devices ensures that we have the right solution for your application.

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Samplicity® G2 Filtration System with Millex Samplicity® and Millex® Filters

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