Product Images
Sterile Opticap XL Capsule Filter
Description:
Opticap Sterile XL05 Millipore Express SHC 0.5 + 0.2 µm 1-1/2 in. TC/TC
Trade Name:
Opticap
Qty/Pk:
1
Key Applications:
Laboratory Filtration
Maximum Inlet Temperature, °C:
25
Outlet Connection Diameter (in):
1-1/2
Inlet Connection Diameter (in):
1-1/2
Outlet Connection:
Sanitary Flange
Maximum Inlet Pressure, bar (psi):
6.9 (100) intermittent @ 25 °C; 5.5 (80) @ 25 °C; 2.75 (40) @ 60 °C; 1.0 (15) @ 80 °C
Maximum Inlet Pressure (psig):
80
Filtration Area, m²:
0.24
Maximum Differential Pressure, bar (psid):
Forward: 6.9 (100) intermittent @ 25 °C; 5.5 (80) @ 25 °C; 1.0 (15) @ 80 °C. Reverse: 2.1 (30) @ 25 °C, intermittent
Inlet Connection:
Sanitary Flange
Diameter, cm (in):
10.7 (4.2)
Oxidizable Substances:
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L
Bubble Point at 23 °C:
≥4000 mbar (58 psig) air with water
Cartridge Nominal Length, in (cm):
5 (12.5)
TOC/Conductivity:
After sterilization and a controlled water flush of 9.5 L, samples exhibited less than 500 ppb TOC per USP <643> and less than 1.3 µS/cm per USP <645> at 25 °C.
Bacterial Retention:
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
Product Name:
Sterile Opticap XL Capsule Filter
Air Diffusion at 23 °C:
≤14 mL/min @ 2.75 bar (40 psig) in water
Sterility:
Sterile
Bacterial Endotoxins:
Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Device Material:
Polypropylene/Polysulfone
Chemistry:
Hydrophilic Polyethersulfone
Inlet to Outlet Width, cm (in):
21.6 (8.5)
Seal Material:
Silicone
Device Size (in):
5
Pore Size (µm):
0.5 / 0.2
Wettability:
Hydrophilic
Sterilization:
3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
Housing:
Polypropylene
Vent Cap Material:
Polypropylene
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.
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.
Non-Fiber Releasing:
This product was manufactured with a Millipore Express membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Filtration Area, cm²:
2400
Connections, Inlet/Outlet:
38 mm (1-1/2 in.) Sanitary Flange
Length, cm (in):
21.6 (8.5)
Connections, Vent/Drain:
1/4 in. Hose Barb with double O-ring seal
Configuration:
Capsule
Support Material:
Polyester
Packaging:
Double Easy-Open bag