Sterile Opticap XLT Capsule Filter
Description:
Opticap Sterile Multilayer XLT20 Durapore 0.45/0.22 µm 1 in. HB/HB
Trade Name:
Opticap
Qty/Pk:
1
Key Applications:
Laboratory Filtration
Maximum Inlet Temperature, °C:
25
Outlet Connection Diameter (in):
1
Inlet Connection Diameter (in):
1
Outlet Connection:
Hose Barb
Maximum Inlet Pressure, bar (psi):
5.5 (80) @ 23 °C; 2.75 (40) @ 60 °C; 1.0 (15) @ 80 °C
Maximum Inlet Pressure (psig):
80
Filtration Area, m²:
1.2
Maximum Differential Pressure, bar (psid):
Forward: 5.5 (80) @ 25 °C; 1.05 (15) @ 80 °C. Reverse: 3.5 (50) @ 25 °C, intermittent
Inlet Connection:
Hose Barb
Diameter, cm (in):
10.7 (4.2)
Oxidizable Substances:
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥3 L
Bubble Point at 23 °C:
≥3450 mbar (50 psig) air with water
Cartridge Nominal Length, in (cm):
20 (50)
TOC/Conductivity:
After sterilization and a controlled water flush, samples exhibited less than 500 ppb TOC per USP <643> and less than 1.3 µS/cm per USP <645> at 25 ºC.
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 XLT Capsule Filter
Air Diffusion at 23 °C:
≤30.0 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
Chemistry:
Hydrophilic PVDF
Media:
Durapore®
Inlet to Outlet Width, cm (in):
19.8 (7.8)
T-line/Gauge Port:
T-line
Seal Material:
Silicone
Device Size (in):
20
Pore Size (µm):
0.45 / 0.22
Wettability:
Hydrophilic
Sterilization:
3 autoclave cycles of 60 min @ 126 °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 Durapore membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Filtration Area, cm²:
12000
Connections, Inlet/Outlet:
25 mm (1 in.) Hose Barb
Length, cm (in):
62.5 (24.6)
Connections, Vent/Drain:
1/4 in. Hose Barb with double O-ring Seal
Configuration:
Capsule
Support Material:
Polypropylene
Packaging:
Double Easy-Open bag