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Opticap XL Capsule Filter
Description:
Opticap XL10 Durapore 0.45 µm without prefilter 3/4 in. TC/TC
Trade Name:
Opticap
Qty/Pk:
1
Key Applications:
Laboratory Filtration
Maximum Inlet Temperature, °C:
25
Outlet Connection Diameter (in):
3/4
Inlet Connection Diameter (in):
3/4
Outlet Connection:
Sanitary Flange
Maximum Inlet Pressure, bar (psi):
5.5 (80) @ 23 °C; 2.8 (40) @ 60 °C; 1.0 (15) @ 80 °C
Maximum Inlet Pressure (psig):
80
Filtration Area, m²:
0.69
Maximum Differential Pressure, bar (psid):
Forward: 3.4 (50) @ 25 °C. Reverse: 3.4 (50) @ 25 °C, intermittent
Diameter, cm (in):
10.7 (4.2)
Inlet Connection:
Sanitary Flange
Oxidizable Substances:
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L
Bubble Point at 23 °C:
≥1930 mbar (28 psig) air with water
Cartridge Nominal Length, in (cm):
10 (25)
Pore Size (µm):
0.45
Wettability:
Hydrophilic
Sterilization:
3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable
Housing:
Polypropylene
Good Manufacturing Practices:
This product was manufactured in a facility which adheres to Good Manufacturing Practices.
Vent Cap Material:
Polypropylene
Indirect Food Additive:
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
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.
Gravimetric Extractables:
The extractables level was equal to or less than 25 mg per capsule after 24 hours in water at controlled room temperature.
Air Diffusion at 23 °C:
≤15 mL/min @ 1.5 bar (22 psig) in water
Product Name:
Opticap XL Capsule 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).
Filtration Area, cm²:
6900
Sterility:
Non-Sterile
Bacterial Endotoxins:
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Device Material:
Polypropylene
Connections, Inlet/Outlet:
19 mm (3/4 in.) Sanitary Flange
Length, cm (in):
33.0 (13.0)
Connections, Vent/Drain:
1/4 in. Hose Barb with double O-ring Seal
Configuration:
Capsule
Chemistry:
Hydrophilic PVDF
Media:
Durapore®
Support Material:
Polypropylene
Inlet to Outlet Width, cm (in):
33.0 (13.0)
Packaging:
Double Easy-Open bag
Seal Material:
Silicone
Device Size (in):
10