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.
Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Bacterial Retention
Quantitative retention of 107 CFU/cm2 Brevundimonas diminuta (ATCC® 19146) per HIMA® methodology
Cartridge Nominal Length
10 in. (25 cm)
Catalogue Number
KHGEG1TTB1H
Chemistry
Hydrophilic Polyethersulfone (PES)
Device Material
Polypropylene/Polysulfone
Device Size
10 in.
Diameter
10.7 in. (4.2 cm)
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
10000 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.
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
Outlet Connection Diameter
1 in.
Oxidizable Substances
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L
Pore Size
0.5 / 0.2 µm
Seal Material
Silicone (SI)
Sterility
Non-Sterile
Sterilization
Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Bacterial Retention
Quantitative retention of 107 CFU/cm2 Brevundimonas diminuta (ATCC® 19146) per HIMA® methodology
Cartridge Nominal Length
10 in. (25 cm)
Catalogue Number
KHGEG1TTB1H
Chemistry
Hydrophilic Polyethersulfone (PES)
Device Material
Polypropylene/Polysulfone
Device Size
10 in.
Diameter
10.7 in. (4.2 cm)
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
10000 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.
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
Outlet Connection Diameter
1 in.
Oxidizable Substances
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L
Pore Size
0.5 / 0.2 µm
Seal Material
Silicone (SI)
Sterility
Non-Sterile
Sterilization
Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
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
10 in. (25 cm)
Catalogue Number
KHGEG1TTT1H
Chemistry
Hydrophilic Polyethersulfone (PES)
Device Material
Polypropylene/Polysulfone
Device Size
10 in.
Diameter
10.7 in. (4.2 cm)
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
10000 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.
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
1.5 in.
Overview
Family (FID): Express (FID19B),Organism Retention: MicroorganismMode of Action: Filtration (size exclusion)Application: BioProcessingIntended Use: Reduction or removal of microorganism/bioburdenInstructions for Use: Please refer installation section of Opticap® XL Capsules and Opticap® XLT Capsules User Guide.Storage Statement: Store in dry location.Disposal Statement: Dispose of in accordance with applicable federal, state, and local regulations.Label statement: Directions for use refer to website.Label statement: Directions for Use refer Opticap® XL Capsules and Opticap® XLT Capsules User Guide on website (custom product only).
Oxidizable Substances
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L
Pore Size
0.5 / 0.2 µm
Seal Material
Silicone (SI)
Sterility
Non-Sterile
Sterilization
Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
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
10 in. (25 cm)
Catalogue Number
KHGEG1TTT1H
Chemistry
Hydrophilic Polyethersulfone (PES)
Device Material
Polypropylene/Polysulfone
Device Size
10 in.
Diameter
10.7 in. (4.2 cm)
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
10000 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.
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
1.5 in.
Overview
Family (FID): Express (FID19B),Organism Retention: MicroorganismMode of Action: Filtration (size exclusion)Application: BioProcessingIntended Use: Reduction or removal of microorganism/bioburdenInstructions for Use: Please refer installation section of Opticap® XL Capsules and Opticap® XLT Capsules User Guide.Storage Statement: Store in dry location.Disposal Statement: Dispose of in accordance with applicable federal, state, and local regulations.Label statement: Directions for use refer to website.Label statement: Directions for Use refer Opticap® XL Capsules and Opticap® XLT Capsules User Guide on website (custom product only).
Oxidizable Substances
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L
Pore Size
0.5 / 0.2 µm
Seal Material
Silicone (SI)
Sterility
Non-Sterile
Sterilization
Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
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.
+852-3069 6950
css@gugent.com.hk
