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
	CR01F2006	Polygard-CR Cartridge Filter 20 in. 1.0 µm Code F	439	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Code Code F double open end w/flat gaskets Cartridge Nominal Length 20 in. (50 cm) Catalogue Number CR01F2006 Chemistry Polypropylene (PP) Device Configuration Cartridge Device Material Polypropylene Diameter 7.0 cm (2.75 in.) Gravimetric Extractables ≤50 mg after 24-h soak in water Length 20 in. (50 cm) Material Size 6 Maximum Differential Pressure, bar (psid) 4.8 bar (70 psid) @ 25 °C Maximum Inlet Pressure, bar (psi) 4.8 bar (70 psi) @ 25 °C Nominal Pore Size 1.0 µm Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥10 L Pore Size 1.0 µm Sanitization 30 min with hot water @ 80 °C Seal Material Polyethylene (PE) Sterilization Do not autoclave Trade Name Polygard® Wettability Hydrophilic
	CR03F2006	Polygard-CR Cartridge Filter 20 in. 3.0 µm Code F	439	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Code Code F double open end w/flat gaskets Cartridge Nominal Length 20 in. (50 cm) Catalogue Number CR03F2006 Chemistry Polypropylene (PP) Device Configuration Cartridge Device Material Polypropylene Diameter 7.0 cm (2.75 in.) Gravimetric Extractables ≤50 mg after 24-h soak in water Length 20 in. (50 cm) Material Size 6 Maximum Differential Pressure, bar (psid) 4.8 bar (70 psid) @ 25 °C Maximum Inlet Pressure, bar (psi) 4.8 bar (70 psi) @ 25 °C Nominal Pore Size 3.0 µm Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥10 L Pore Size 3.0 µm Sanitization 30 min with hot water @ 80 °C Seal Material Polyethylene (PE) Sterilization Do not autoclave Trade Name Polygard® Wettability Hydrophilic
	CR03F2006	Polygard-CR Cartridge Filter 20 in. 3.0 µm Code F	439	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Code Code F double open end w/flat gaskets Cartridge Nominal Length 20 in. (50 cm) Catalogue Number CR03F2006 Chemistry Polypropylene (PP) Device Configuration Cartridge Device Material Polypropylene Diameter 7.0 cm (2.75 in.) Gravimetric Extractables ≤50 mg after 24-h soak in water Length 20 in. (50 cm) Material Size 6 Maximum Differential Pressure, bar (psid) 4.8 bar (70 psid) @ 25 °C Maximum Inlet Pressure, bar (psi) 4.8 bar (70 psi) @ 25 °C Nominal Pore Size 3.0 µm Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥10 L Pore Size 3.0 µm Sanitization 30 min with hot water @ 80 °C Seal Material Polyethylene (PE) Sterilization Do not autoclave Trade Name Polygard® Wettability Hydrophilic
	CR05F2006	Polygard-CR Cartridge Filter 20 in. 5.0 µm Code F	439	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Code Code F double open end w/flat gaskets Cartridge Nominal Length 20 in. (50 cm) Catalogue Number CR05F2006 Chemistry Polypropylene (PP) Device Configuration Cartridge Device Material Polypropylene Diameter 7.0 cm (2.75 in.) Gravimetric Extractables ≤50 mg after 24-h soak in water Length 20 in. (50 cm) Material Size 6 Maximum Differential Pressure, bar (psid) 4.8 bar (70 psid) @ 25 °C Maximum Inlet Pressure, bar (psi) 4.8 bar (70 psi) @ 25 °C Nominal Pore Size 5.0 µm Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥10 L Pore Size 5.0 µm Sanitization 30 min with hot water @ 80 °C Seal Material Polyethylene (PE) Sterilization Do not autoclave Trade Name Polygard® Wettability Hydrophilic
	CR05F2006	Polygard-CR Cartridge Filter 20 in. 5.0 µm Code F	439	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Code Code F double open end w/flat gaskets Cartridge Nominal Length 20 in. (50 cm) Catalogue Number CR05F2006 Chemistry Polypropylene (PP) Device Configuration Cartridge Device Material Polypropylene Diameter 7.0 cm (2.75 in.) Gravimetric Extractables ≤50 mg after 24-h soak in water Length 20 in. (50 cm) Material Size 6 Maximum Differential Pressure, bar (psid) 4.8 bar (70 psid) @ 25 °C Maximum Inlet Pressure, bar (psi) 4.8 bar (70 psi) @ 25 °C Nominal Pore Size 5.0 µm Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥10 L Pore Size 5.0 µm Sanitization 30 min with hot water @ 80 °C Seal Material Polyethylene (PE) Sterilization Do not autoclave Trade Name Polygard® Wettability Hydrophilic
	KWSCA3THH1	Opticap® XLT30 Milligard® 1.2/0.5 µm 5/8 in. HB/HB	439	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 KWSCA3THH1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 5/8 in. Filter Grade Standard Milligard® Media Filtration Area 2.07 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 165 mg per capsule after 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 Housing Material Nominal Pore Size 1.2 / 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 1.2 / 0.5 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polyester 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.)
	KWSCA3THH1	Opticap® XLT30 Milligard® 1.2/0.5 µm 5/8 in. HB/HB	439	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 KWSCA3THH1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 5/8 in. Filter Grade Standard Milligard® Media Filtration Area 2.07 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 165 mg per capsule after 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 Housing Material Nominal Pore Size 1.2 / 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 1.2 / 0.5 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polyester 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.)
	KWSCA3TTT1	Opticap® XLT30 Milligard® 1.2/0.5 µm 1-1/2 in. TC/TC	439	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 KWSCA3TTT1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 1-1/2 in. Filter Grade Standard Milligard® Media Filtration Area 2.07 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 165 mg per capsule after 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 Housing Material Nominal Pore Size 1.2 / 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 1.2 / 0.5 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polyester 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.)
	KWSCA3TTT1	Opticap® XLT30 Milligard® 1.2/0.5 µm 1-1/2 in. TC/TC	439	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 KWSCA3TTT1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 1-1/2 in. Filter Grade Standard Milligard® Media Filtration Area 2.07 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 165 mg per capsule after 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 Housing Material Nominal Pore Size 1.2 / 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 1.2 / 0.5 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polyester 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.)
	KWSSA3THH1	Opticap® XLT30 Milligard® 0.5/0.2 µm 5/8 in. HB/HB	439	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 KWSSA3THH1 Chemistry Mixed Cellulose Esters (MCE) Device Configuration Capsule Device Material Polypropylene Device Size 30 in. Diameter 5/8 in. Filter Grade Standard Milligard® Media Filtration Area 2.07 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 165 mg per capsule after 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 Housing Material Nominal Pore Size 0.5 / 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 0.5 / 0.2 µm Seal Material Silicone (SI) Sterilization 3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable Support Material Polyester 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.)

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