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
	PXGVPPC50	Pellicon® XL50 with Durapore® 0.22 µm Membrane, C screen, 50 cm²	244	Add to Cart
Catalogue Number PXGVPPC50 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cassette Device Material Polypropylene Filter Code GVPP Filter Type Microfiltration Filtration Area 50 cm² 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 7.5 mg per device after a water flush Hold-up Volume 3.2 mL Key Applications Protein PurificationAnalytical Sample Prep Length 18.8 cm (7.4 in.) Material Package Each Pellicon® XL50 cassette is packaged one per box and includes Operating Instructions, an Accessory Kit and a Certificate of Quality Material Size 1 Maximum Inlet Pressure, bar (psi) 5.5 bar (80 psi) @ 50 °C Maximum Transmembrane Pressure 2.8 bar (40 psig) Media Durapore® Membrane Area 50 cm² Minimum Working Volume 15 mL pH Range pH1.5 – pH9 continuous; pH1 – pH11 cleaning Pore Size 0.22 µm Recirculation Rate 0.03–0.05 L/min Screen Material Polypropylene, Thermoplastic Elastomer Screen Type Type C screen (coarse screen) Trade Name Pellicon® Volume 3.2 mL Width 3 cm (1.2 in.)
	PXHVMPC50	Pellicon® XL50 with Durapore® 0.45 µm Membrane, C screen, 50 cm²	244	Add to Cart
Catalogue Number PXHVMPC50 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cassette Device Material Polypropylene Filter Code HVMP Filter Type Microfiltration Filtration Area 50 cm² 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 7.5 mg per device after a water flush Hold-up Volume 3.2 mL Key Applications Protein PurificationAnalytical Sample Prep Length 18.8 cm (7.4 in.) Material Package Each Pellicon® XL50 cassette is packaged one per box and includes Operating Instructions, an Accessory Kit and a Certificate of Quality Material Size 1 Maximum Inlet Pressure, bar (psi) 5.5 bar (80 psi) @ 50 °C Maximum Transmembrane Pressure 2.8 bar (40 psig) Media Durapore® Membrane Area 50 cm² Minimum Working Volume 15 mL pH Range pH1.5 – pH9 continuous; pH1 – pH11 cleaning Pore Size 0.45 µm Recirculation Rate 0.03–0.05 L/min Screen Material Polypropylene, Thermoplastic Elastomer Screen Type Type C screen (coarse screen) Trade Name Pellicon® Volume 3.2 mL Width 3 cm (1.2 in.)
	PXHVMPC50	Pellicon® XL50 with Durapore® 0.45 µm Membrane, C screen, 50 cm²	244	Add to Cart
Catalogue Number PXHVMPC50 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cassette Device Material Polypropylene Filter Code HVMP Filter Type Microfiltration Filtration Area 50 cm² 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 7.5 mg per device after a water flush Hold-up Volume 3.2 mL Key Applications Protein PurificationAnalytical Sample Prep Length 18.8 cm (7.4 in.) Material Package Each Pellicon® XL50 cassette is packaged one per box and includes Operating Instructions, an Accessory Kit and a Certificate of Quality Material Size 1 Maximum Inlet Pressure, bar (psi) 5.5 bar (80 psi) @ 50 °C Maximum Transmembrane Pressure 2.8 bar (40 psig) Media Durapore® Membrane Area 50 cm² Minimum Working Volume 15 mL pH Range pH1.5 – pH9 continuous; pH1 – pH11 cleaning Pore Size 0.45 µm Recirculation Rate 0.03–0.05 L/min Screen Material Polypropylene, Thermoplastic Elastomer Screen Type Type C screen (coarse screen) Trade Name Pellicon® Volume 3.2 mL Width 3 cm (1.2 in.)
	PXVVPPC50	Pellicon® XL50 with Durapore® 0.1 µm Membrane, C screen, 50 cm²	244	Add to Cart
Catalogue Number PXVVPPC50 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cassette Device Material Polypropylene Filter Code VVPP Filter Type Microfiltration Filtration Area 50 cm² 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 7.5 mg per device after a water flush Hold-up Volume 3.2 mL Key Applications Protein PurificationAnalytical Sample Prep Length 18.8 cm (7.4 in.) Material Package Each Pellicon® XL50 cassette is packaged one per box and includes Operating Instructions, an Accessory Kit and a Certificate of Quality Material Size 1 Maximum Inlet Pressure, bar (psi) 5.5 bar (80 psi) @ 50 °C Maximum Transmembrane Pressure 2.8 bar (40 psig) Media Durapore® Membrane Area 50 cm² Minimum Working Volume 15 mL pH Range pH1.5 – pH9 continuous; pH1 – pH11 cleaning Pore Size 0.1 µm Recirculation Rate 0.03–0.05 L/min Screen Material Polypropylene, Thermoplastic Elastomer Screen Type Type C screen (coarse screen) Trade Name Pellicon® Volume 3.2 mL Width 3 cm (1.2 in.)
	PXVVPPC50	Pellicon® XL50 with Durapore® 0.1 µm Membrane, C screen, 50 cm²	244	Add to Cart
Catalogue Number PXVVPPC50 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cassette Device Material Polypropylene Filter Code VVPP Filter Type Microfiltration Filtration Area 50 cm² 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 7.5 mg per device after a water flush Hold-up Volume 3.2 mL Key Applications Protein PurificationAnalytical Sample Prep Length 18.8 cm (7.4 in.) Material Package Each Pellicon® XL50 cassette is packaged one per box and includes Operating Instructions, an Accessory Kit and a Certificate of Quality Material Size 1 Maximum Inlet Pressure, bar (psi) 5.5 bar (80 psi) @ 50 °C Maximum Transmembrane Pressure 2.8 bar (40 psig) Media Durapore® Membrane Area 50 cm² Minimum Working Volume 15 mL pH Range pH1.5 – pH9 continuous; pH1 – pH11 cleaning Pore Size 0.1 µm Recirculation Rate 0.03–0.05 L/min Screen Material Polypropylene, Thermoplastic Elastomer Screen Type Type C screen (coarse screen) Trade Name Pellicon® Volume 3.2 mL Width 3 cm (1.2 in.)
	D003P3S01	Clarigard Cartridge Filter 30 in. 0.3 µm Code P Silicone	245	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Code Code P double open end w/flat gaskets Cartridge Nominal Length 30 in. (75 cm) Catalogue Number D003P3S01 Chemistry Polypropylene (PP) Device Configuration Cartridge Device Material Polypropylene Diameter 7.0 cm (2.75 in.) Gravimetric Extractables ≤30 mg after 24-h soak in water Length 30 in. (75 cm) Material Size 1 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 0.3 µm Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥9 L Pore Size 0.3 µm Seal Material Silicone (SI) Sterilization 10 autoclave cycles or SIP @ 126 °C for 30 min Trade Name Clarigard® Wettability Hydrophilic
	D003P3S01	Clarigard Cartridge Filter 30 in. 0.3 µm Code P Silicone	245	Add to Cart
Bacterial Endotoxins Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test Cartridge Code Code P double open end w/flat gaskets Cartridge Nominal Length 30 in. (75 cm) Catalogue Number D003P3S01 Chemistry Polypropylene (PP) Device Configuration Cartridge Device Material Polypropylene Diameter 7.0 cm (2.75 in.) Gravimetric Extractables ≤30 mg after 24-h soak in water Length 30 in. (75 cm) Material Size 1 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 0.3 µm Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥9 L Pore Size 0.3 µm Seal Material Silicone (SI) Sterilization 10 autoclave cycles or SIP @ 126 °C for 30 min Trade Name Clarigard® Wettability Hydrophilic
	KHGEG003HB3	Opticap® Gamma Compatible XL 300 Millipore Express® SHC 0.5/0.2 µm 9/16 in. HB/HB with Bell	245	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 4.7 in. (11.9 cm) Catalogue Number KHGEG003HB3 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Diameter 5.6 cm (2.2 in.) European Pressure Equipment Directive EMD Millipore Corporation® certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark. Filtration Area 290 cm² 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 9/16 in. Inlet to Outlet Width 11.9 cm (4.7 in.) Length 4.7 in. (11.9 cm) Material Package Double Easy-Open bag Material Size 3 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® SHC 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 with Bell Outlet Connection Diameter 9/16 in. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L Pore Size 0.5 / 0.2 µm Seal Material Silicone (SI) Sterility Gamma Sterilization Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyethylene 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 11.9 cm (4.7 in.)
	KHGEG003HB3	Opticap® Gamma Compatible XL 300 Millipore Express® SHC 0.5/0.2 µm 9/16 in. HB/HB with Bell	245	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 4.7 in. (11.9 cm) Catalogue Number KHGEG003HB3 Chemistry Polyethersulfone (PES) Device Configuration Capsule Device Material Gamma stable polypropylene/Polysulfone Diameter 5.6 cm (2.2 in.) European Pressure Equipment Directive EMD Millipore Corporation® certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark. Filtration Area 290 cm² 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 9/16 in. Inlet to Outlet Width 11.9 cm (4.7 in.) Length 4.7 in. (11.9 cm) Material Package Double Easy-Open bag Material Size 3 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® SHC 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 with Bell Outlet Connection Diameter 9/16 in. Oxidizable Substances Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L Pore Size 0.5 / 0.2 µm Seal Material Silicone (SI) Sterility Gamma Sterilization Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable Support Material Polyethylene 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 11.9 cm (4.7 in.)
	CVVL75S01	Durapore® Cartridge Filter 5 in. 0.1 µm Code 7	247	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 5 in. (12.5 cm) Catalogue Number CVVL75S01 Chemistry Polyvinylidene Fluoride (PVDF) Device Configuration Cartridge Device Material Polypropylene Device Size 5 in. Diameter 6.9 cm (2.7 in.) Filtration Area 0.35 m² Flow Rate 7.5 L/min @ 700 mbar ΔP Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices. 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 5 in. (12.5 cm) Material Package Double Easy-Open bag Material Size 1 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 ≥500 mL Pore Size 0.1 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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