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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
PXC300C50 Pellicon® XL50 with Ultracel® 300 kDa Membrane, C screen, 50 cm² USD 232 
Add to Cart
  • Catalogue Number
  • PXC300C50
  • Chemistry
  • Composite Regenerated Cellulose (CRC)
  • Device Configuration
  • Cassette
  • Device Material
  • Polypropylene
  • Filter Code
  • PLCMK
  • Filter Type
  • Ultrafiltration
  • 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
  • Ultracel®
  • Membrane Area
  • 50 cm²
  • Minimum Working Volume
  • 15 mL
  • NMWL
  • 300 kDa
  • pH Range
  • pH2 – pH12 continuous; pH2 – pH13 cleaning
  • 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.)
SK1M004W01 Pellicon® XL50 with Biomax® 5 kDa Membrane, C Screen, 50 cm² USD 232 
Add to Cart
  • Catalogue Number
  • SK1M004W01
  • Chemistry
  • Polyethersulfone (PES)
  • Device Configuration
  • Cassette
  • Device Material
  • Polypropylene
  • Filter Code
  • Biomax 5
  • Filter Type
  • Ultrafiltration
  • 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
  • Biomax®
  • Membrane Area
  • 50 cm²
  • NMWL
  • 5 kDa
  • pH Range
  • pH1 – pH14 continuous; pH1 – pH14 cleaning
  • 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.)
SK1M005W01 Pellicon® XL50 with Biomax® 8 kDa Membrane, C Screen, 50 cm² USD 232 
Add to Cart
  • Catalogue Number
  • SK1M005W01
  • Chemistry
  • Polyethersulfone (PES)
  • Device Configuration
  • Cassette
  • Device Material
  • Polypropylene
  • Filter Code
  • Biomax 8
  • Filter Type
  • Ultrafiltration
  • 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
  • Biomax®
  • Membrane Area
  • 50 cm²
  • NMWL
  • 8 kDa
  • pH Range
  • pH1 – pH14 continuous; pH1 – pH14 cleaning
  • 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.)
SK1M006W01 Pellicon® XL50 with Biomax® 10 kDa Membrane, C Screen, 50 cm² USD 232 
Add to Cart
  • Catalogue Number
  • SK1M006W01
  • Chemistry
  • Polyethersulfone (PES)
  • Device Configuration
  • Cassette
  • Device Material
  • Polypropylene
  • Filter Code
  • Biomax 10
  • Filter Type
  • Ultrafiltration
  • 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
  • Biomax®
  • Membrane Area
  • 50 cm²
  • NMWL
  • 10 kDa
  • pH Range
  • pH1 – pH14 continuous; pH1 – pH14 cleaning
  • 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.)
SK1M007W01 Pellicon® XL50 with Biomax® 30 kDa Membrane, C Screen, 50 cm² USD 232 
Add to Cart
  • Catalogue Number
  • SK1M007W01
  • Chemistry
  • Polyethersulfone (PES)
  • Device Configuration
  • Cassette
  • Device Material
  • Polypropylene
  • Filter Code
  • Biomax 30
  • Filter Type
  • Ultrafiltration
  • 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
  • Biomax®
  • Membrane Area
  • 50 cm²
  • NMWL
  • 30 kDa
  • pH Range
  • pH1 – pH14 continuous; pH1 – pH14 cleaning
  • 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.)
SK1M008W01 Pellicon® XL50 with Biomax® 50 kDa Membrane, C Screen, 50 cm² USD 232 
Add to Cart
  • Catalogue Number
  • SK1M008W01
  • Chemistry
  • Polyethersulfone (PES)
  • Device Configuration
  • Cassette
  • Device Material
  • Polypropylene
  • Filter Code
  • Biomax 50
  • Filter Type
  • Ultrafiltration
  • 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
  • Biomax®
  • Membrane Area
  • 50 cm²
  • NMWL
  • 50 kDa
  • pH Range
  • pH1 – pH14 continuous; pH1 – pH14 cleaning
  • 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.)
XXRES05ST Stand for 100 mL Reservoir USD 232 
Add to Cart
  • Catalogue Number
  • XXRES05ST
  • Material Size
  • 1
  • Trade Name
  • Pellicon®
KVEPS015FF3 Opticap® Sterile XL 150 Millipore Express® SHR single layer 0.1 µm 3/4 in. TC/TC USD 234 
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
  • 3.8 in. (9.7 cm)
  • Catalogue Number
  • KVEPS015FF3
  • Chemistry
  • Polyethersulfone (PES)
  • Device Configuration
  • Capsule
  • Device Material
  • Polypropylene
  • 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
  • 250 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
  • Sanitary Flange
  • Inlet Connection Diameter
  • 3/4 in.
  • Inlet to Outlet Width
  • 9.7 cm (3.8 in.)
  • Length
  • 3.8 in. (9.7 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® SHR
  • 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
  • Sanitary Flange
  • Outlet Connection Diameter
  • 3/4 in.
  • Oxidizable Substances
  • Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L
  • Pore Size
  • 0.1 µm
  • Seal Material
  • Silicone (SI)
  • Sterility
  • Sterile
  • Sterilization
  • 3 autoclave cycles of 60 min @ 123 °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
  • 9.7 cm (3.8 in.)
KVEPS015FF3 Opticap® Sterile XL 150 Millipore Express® SHR single layer 0.1 µm 3/4 in. TC/TC USD 234 
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
  • 3.8 in. (9.7 cm)
  • Catalogue Number
  • KVEPS015FF3
  • Chemistry
  • Polyethersulfone (PES)
  • Device Configuration
  • Capsule
  • Device Material
  • Polypropylene
  • 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
  • 250 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
  • Sanitary Flange
  • Inlet Connection Diameter
  • 3/4 in.
  • Inlet to Outlet Width
  • 9.7 cm (3.8 in.)
  • Length
  • 3.8 in. (9.7 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® SHR
  • 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
  • Sanitary Flange
  • Outlet Connection Diameter
  • 3/4 in.
  • Oxidizable Substances
  • Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L
  • Pore Size
  • 0.1 µm
  • Seal Material
  • Silicone (SI)
  • Sterility
  • Sterile
  • Sterilization
  • 3 autoclave cycles of 60 min @ 123 °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
  • 9.7 cm (3.8 in.)
MCGL10S03 Millidisk® Cartridge 10-stack 0.22 µm Hydrophilic USD 234 
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
  • Not Applicable
  • Catalogue Number
  • MCGL10S03
  • Chemistry
  • Polyvinylidene Fluoride (PVDF)
  • Device Configuration
  • Cartridge
  • Device Material
  • Polysulfone
  • Filtration Area
  • 500 cm²
  • Flow Rate
  • 15 L/min @ 3.5 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 2.5 mg per sterilized device after 24 hours in water at controlled room temperature.
  • Material Package
  • Double Easy-Open bag
  • 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)
  • Forward - 4.1 bar (60 psi) @ 25 °C; 1.7 bar (25 psi) @ 80 °C; 0.35 bar (5 psi) @ 123 °C; Reverse - 0.7 bar (10 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 ≥200 mL
  • Pore Size
  • 0.22 µm
  • Seal Material
  • Silicone (SI)
  • Sterility
  • Other
  • Sterilization
  • 5 SIP cycles of 60 min @ 135 °C; 5 autoclave cycles of 60 min @ 126 °C
  • Support Material
  • Polysulfone
  • Trade Name
  • Millidisk®
  • 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

Overview

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