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Bacterial Endotoxins
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
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Cartridge Code
Code 7 (2-226) O-rings w/locking-tabs
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Cartridge Nominal Length
20 in. (50 cm)
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Catalogue Number
CVDR72TP3
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Chemistry
Polyvinylidene Fluoride (PVDF)
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Device Configuration
Cartridge
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Device Material
Polypropylene
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Device Size
20 in.
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Diameter
6.9 cm (2.7 in.)
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Filtration Area
1.38 m²
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Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
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Gravimetric Extractables
The extractables level was equal to or less than 45 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
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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.
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Length
20 in. (50 cm)
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Material Package
Double Easy-Open bag
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Material Size
3
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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: 1.7 bar (25 psid) @ 25 °C
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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 - 1.7 bar (25 psi) @ 25 °C
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Media
Durapore® w/Prefilter
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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).
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Oxidizable Substances
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L
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Pore Size
0.65 µm
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Seal Material
Silicone (SI)
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Sterility
Other
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Sterilization
8 SIP cycles of 30 min or 8 autoclave cycles of 60 min @ 121 °C
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Support Material
Polypropylene
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Trade Name
Durapore®
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USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
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Wettability
Hydrophilic
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