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Durapore Cartridge Filter
Description:
Durapore Cartridge Filter without prefilter 20 in. 0.45 µm Code 0
Trade Name:
Durapore
Qty/Pk:
3
Key Applications:
Laboratory Filtration
Filtration Area, m²:
1.38
Maximum Differential Pressure, bar (psid):
Forward: 5.5 (80) @ 25 °C; 1.7 (25) @ 80 °C; 0.35 (5) @ 135 °C. Reverse: 3.5 (50) @ 25 °C
Diameter, cm (in):
6.9 (2.7)
Oxidizable Substances:
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L
Bubble Point at 23 °C:
≥1930 mbar (28 psig) air with water
Cartridge Nominal Length, in (cm):
20 (50)
Pore Size (µm):
0.45
Wettability:
Hydrophilic
Sterilization:
30 SIP cycles of 30 min @ 135 °C; 30 autoclave cycles of 60 min @ 126 °C
Good Manufacturing Practices:
This product was manufactured in a facility which adheres to Good Manufacturing Practices.
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.
Gravimetric Extractables:
The extractables level was equal to or less than 20 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
Air Diffusion at 23 °C:
≤30 mL/min @ 1.5 bar (22 psig) in water
Product Name:
Durapore Cartridge Filter
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).
Bacterial Endotoxins:
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Device Material:
Polypropylene
Configuration:
Cartridge
Chemistry:
Hydrophilic PVDF
Cartridge Code:
Code 0 (2-222) O-rings
Media:
Durapore®
Support Material:
Polypropylene
Packaging:
Double Easy-Open bag
Code:
Code 0
Seal Material:
Silicone
Device Size (in):
20