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.
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 23 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
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.
Key Applications
Food and BeverageBeerBottled WaterWine
Length
30 in. (75 cm)
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) @ 109 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent
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) @ 109 °C. Reverse - 3.5 bar (50 psi) @ 25 °C, Intermittent
Media
Vitipore® II
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).
Pore Size
0.45 µm
Seal Material
Silicone (SI)
Sterility
Other
Sterilization
100 SIP cycles of 30 min @ 109 °C; hot water sanitized 50 times for 30 min @ 80 °C maximum
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 23 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
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.
Key Applications
Food and BeverageBeerBottled WaterWine
Length
30 in. (75 cm)
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) @ 109 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent
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) @ 109 °C. Reverse - 3.5 bar (50 psi) @ 25 °C, Intermittent
Media
Vitipore® II
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).
Pore Size
0.45 µm
Seal Material
Silicone (SI)
Sterility
Other
Sterilization
100 SIP cycles of 30 min @ 109 °C; hot water sanitized 50 times for 30 min @ 80 °C maximum
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 23 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
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.
Key Applications
Food and BeverageBeerBottled WaterWine
Length
40 in. (100 cm)
Material Size
3
Media
Vitipore® II
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).
Microbial titer reduction >1011 CFU/cartridge when challenged with Saccharomyces cerevisae; >107 CFU/cartridge with Pediococcus damnosus; >106 CFU/cartridge with Lactobacillus brevis
Cartridge Code
Code 7 (2-226) O-rings w/locking-tabs
Cartridge Nominal Length
10 in. (25 cm)
Catalogue Number
CVBH71PK1
Chemistry
Hydrophobic Polyvinylidene Fluoride (PVDF)
Device Configuration
Cartridge
Device Material
Polypropylene
Diameter
6.9 cm (2.7 in.)
Filtration Area
0.75 m²
Flow Rate
20 L/min @ 330 mbar ΔP
Key Applications
Food and BeverageBeerBottled WaterWine
Length
10 in. (25 cm)
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) @ 121 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent; 0.35 bar (5 psid) @ 121 °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) @ 121 °C. Reverse - 3.5 bar (50 psi) @ 25 °C, Intermittent; 0.35 bar (5 psi) @ 121 °C
Media
Durapore®
Pore Size
0.55 µm
Seal Material
Silicone (SI)
Sterility
Other
Sterilization
100 SIP cycles of 30 min @ 109 °C; hot water sanitized 50 times for 30 min @ 80 °C maximum
Microbial titer reduction >1011 CFU/cartridge when challenged with Saccharomyces cerevisae; >107 CFU/cartridge with Pediococcus damnosus; >106 CFU/cartridge with Lactobacillus brevis
Cartridge Code
Code 7 (2-226) O-rings w/locking-tabs
Cartridge Nominal Length
10 in. (25 cm)
Catalogue Number
CVBH71PK1
Chemistry
Hydrophobic Polyvinylidene Fluoride (PVDF)
Device Configuration
Cartridge
Device Material
Polypropylene
Diameter
6.9 cm (2.7 in.)
Filtration Area
0.75 m²
Flow Rate
20 L/min @ 330 mbar ΔP
Key Applications
Food and BeverageBeerBottled WaterWine
Length
10 in. (25 cm)
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) @ 121 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent; 0.35 bar (5 psid) @ 121 °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) @ 121 °C. Reverse - 3.5 bar (50 psi) @ 25 °C, Intermittent; 0.35 bar (5 psi) @ 121 °C
Media
Durapore®
Pore Size
0.55 µm
Seal Material
Silicone (SI)
Sterility
Other
Sterilization
100 SIP cycles of 30 min @ 109 °C; hot water sanitized 50 times for 30 min @ 80 °C maximum
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 30 mg per 10-inch cartridge after 24 hours in a 70/30% IPA/water mixture at controlled room temperature.
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.
Key Applications
Food and BeverageBeerBottled WaterWine
Length
20 in. (50 cm)
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) @ 121 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent; 0.35 bar (5 psid) @ 121 °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) @ 121 °C. Reverse - 3.5 bar (50 psi) @ 25 °C, Intermittent; 0.35 bar (5 psi) @ 121 °C
Media
Brewpore®
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).
Pore Size
0.55 µm
Seal Material
Silicone (SI)
Sterility
Other
Sterilization
100 SIP cycles of 30 min @ 109 °C; hot water sanitized 50 times for 30 min @ 80 °C maximum
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 30 mg per 10-inch cartridge after 24 hours in a 70/30% IPA/water mixture at controlled room temperature.
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.
Key Applications
Food and BeverageBeerBottled WaterWine
Length
20 in. (50 cm)
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) @ 121 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent; 0.35 bar (5 psid) @ 121 °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) @ 121 °C. Reverse - 3.5 bar (50 psi) @ 25 °C, Intermittent; 0.35 bar (5 psi) @ 121 °C
Media
Brewpore®
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).
Pore Size
0.55 µm
Seal Material
Silicone (SI)
Sterility
Other
Sterilization
100 SIP cycles of 30 min @ 109 °C; hot water sanitized 50 times for 30 min @ 80 °C maximum
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 23 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
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.
Key Applications
Food and BeverageBeerBottled WaterWine
Length
30 in. (75 cm)
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, intermittent
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, Intermittent
Media
Vitipore® II
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).
Pore Size
0.22 µm
Seal Material
Silicone (SI)
Sterility
Other
Sterilization
100 SIP cycles of 30 min @ 109 °C; hot water sanitized 30 times for 30 min @ 80 °C maximum
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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