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 ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Cartridge Nominal Length
5 in. (12.5 cm)
Catalogue Number
KRA5A05HH1
Chemistry
Polypropylene (PP)
Device Configuration
Capsule
Device Material
Polypropylene
Device Size
5 in.
Diameter
10.7 cm (4.2 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.
Format
Single 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 30 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
9/16 in.
Inlet to Outlet Width
21.6 cm (8.5 in.)
Length
5 in. (12.5 cm)
Material Package
Double Easy-Open bag
Material Size
1
Maximum Differential Pressure, bar (psid)
4.8 bar (70 psid) @ 20 °C
Maximum Inlet Pressure (psig)
80 psig
Maximum Inlet Pressure, bar (psi)
5.5 bar (80 psi) @ 25 °C; 2.75 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C
Maximum Inlet Temperature
25 °C
Media
Polygard®-CR
Nominal Pore Size
0.5 µm
Outlet Connection
Hose Barb
Outlet Connection Diameter
9/16 in.
Oxidizable Substances
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2.5 L
Pore Size
0.5 µm
Seal Material
Silicone (SI)
Sterilization
3 autoclave cycles of 30 min @ 126 °C; not in-line steam sterilizable
Support Material
Polypropylene
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.
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Cartridge Nominal Length
5 in. (12.5 cm)
Catalogue Number
KRA5A05TT1
Chemistry
Polypropylene (PP)
Device Configuration
Capsule
Device Material
Polypropylene
Device Size
5 in.
Diameter
10.7 cm (4.2 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.
Format
Single 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 30 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
21.6 cm (8.5 in.)
Length
5 in. (12.5 cm)
Material Package
Double Easy-Open bag
Material Size
1
Maximum Differential Pressure, bar (psid)
4.8 bar (70 psid) @ 20 °C
Maximum Inlet Pressure (psig)
80 psig
Maximum Inlet Pressure, bar (psi)
5.5 bar (80 psi) @ 25 °C; 2.75 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C
Maximum Inlet Temperature
25 °C
Media
Polygard®-CR
Nominal Pore Size
0.5 µm
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 ≥2.5 L
Pore Size
0.5 µm
Seal Material
Silicone (SI)
Sterilization
3 autoclave cycles of 30 min @ 126 °C; not in-line steam sterilizable
Support Material
Polypropylene
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.
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Cartridge Nominal Length
5 in. (12.5 cm)
Catalogue Number
KRA5A05TT1
Chemistry
Polypropylene (PP)
Device Configuration
Capsule
Device Material
Polypropylene
Device Size
5 in.
Diameter
10.7 cm (4.2 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.
Format
Single 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 30 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
21.6 cm (8.5 in.)
Length
5 in. (12.5 cm)
Material Package
Double Easy-Open bag
Material Size
1
Maximum Differential Pressure, bar (psid)
4.8 bar (70 psid) @ 20 °C
Maximum Inlet Pressure (psig)
80 psig
Maximum Inlet Pressure, bar (psi)
5.5 bar (80 psi) @ 25 °C; 2.75 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C
Maximum Inlet Temperature
25 °C
Media
Polygard®-CR
Nominal Pore Size
0.5 µm
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 ≥2.5 L
Pore Size
0.5 µm
Seal Material
Silicone (SI)
Sterilization
3 autoclave cycles of 30 min @ 126 °C; not in-line steam sterilizable
Support Material
Polypropylene
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.
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Catalogue Number
MPHL02GF2
Chemistry
Polyvinylidene Fluoride (PVDF)
Device Configuration
Gamma Gold Capsule
Device Material
Polycarbonate
Diameter
3/4 in.
Filtration Area
100 cm²
Flow Rate
6.4 L/min @ 2.45 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 1 mg per sterilized device after a 200 mL flush and 24 hours in water at controlled room temperature.
Inlet Connection
Sanitary Flange
Inlet Connection Diameter
3/4 in.
Material Package
Blister
Material Size
2
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)
5.2 bar (75 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).
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 ≥200 mL
Pore Size
0.45 µm
Process Volume
10 L
Sterility
Sterile
Sterilization
3 autoclave cycles of 90 min @ 123 °C; not in-line steam sterilizable
Support Material
Polycarbonate
Trade Name
Millipak®
USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
The Sterifil® aseptic system was designed as a tool for general filtration applications and filtration of samples for particulate or biological contamination analysis. The closed unit protects sample and filtrate from environmental contamination. Sterifil® holder and funnel are available separately (without receiver flask and cover) to use with standard 1 L filter flasks or multiple place manifolds. Depending upon membrane filter selection, the Sterifil® products can be used for a variety of applications including bioburden monitoring and enumeration of organisms in samples. Features & Benefits:•Closed unit protects samples and filtrate from environmental contamination •Device is autoclavable with membrane in place for sterile applications with less waste •Optional hand pump allows for on-site filtration Applications:General Filtration, Field-based Filtration (with optional hand pump), Bioburden Monitoring, Counting Microorganisms, Filtration Processes Requiring Membrane to be Retained
Catalogue Number
XX11J4750
Diameter
8.5 cm
Filter Diameter (⌀)
47 mm
Filtration Area
15.2 cm²
Fitting Inlet
Funnel
Fitting Outlet
Holder outlet stopper fits standard 1 L filtering flask
Height
14.5 cm
Material Size
1
Materials of Construction
Polysulfone funnel, funnel cover, receiver flask and cover; polypropylene holder base and filter support screen; silicone stopper
The Sterifil® aseptic system was designed as a tool for general filtration applications and filtration of samples for particulate or biological contamination analysis. The closed unit protects sample and filtrate from environmental contamination. Sterifil® holder and funnel are available separately (without receiver flask and cover) to use with standard 1 L filter flasks or multiple place manifolds. Depending upon membrane filter selection, the Sterifil® products can be used for a variety of applications including bioburden monitoring and enumeration of organisms in samples. Features & Benefits:•Closed unit protects samples and filtrate from environmental contamination •Device is autoclavable with membrane in place for sterile applications with less waste •Optional hand pump allows for on-site filtration Applications:General Filtration, Field-based Filtration (with optional hand pump), Bioburden Monitoring, Counting Microorganisms, Filtration Processes Requiring Membrane to be Retained
Catalogue Number
XX11J4750
Diameter
8.5 cm
Filter Diameter (⌀)
47 mm
Filtration Area
15.2 cm²
Fitting Inlet
Funnel
Fitting Outlet
Holder outlet stopper fits standard 1 L filtering flask
Height
14.5 cm
Material Size
1
Materials of Construction
Polysulfone funnel, funnel cover, receiver flask and cover; polypropylene holder base and filter support screen; silicone stopper
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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