KHGEG1TTT1H
Millipore Express® SHC High Area, Opticap® XLT Capsule
Opticap® XLT 10, non-sterile, pore size 0.5/0.2 μm, cartridge nominal length 10 in. (25 cm)
Synonym(s):
Gamma Compatible High Area Opticap® XLT 10 Millipore Express® SHC 0.5 µm/0.2 µm 1-1/2 in. TC
About This Item
Recommended Products
material
polyester support
polyethersulfone
polypropylene
polypropylene housing
polypropylene vent cap
polysulfone
silicone seal
Quality Level
reg. compliance
meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
sterility
non-sterile
Sterilization Compatibility
gamma compatible
product line
Opticap® XLT 10
feature
hydrophilic
manufacturer/tradename
Millipore Express®
parameter
≤56.4 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water)
1.0 bar max. differential pressure (15 psi) at 80 °C (Forward)
2.1 bar max. differential pressure (30 psi) at 25 °C (Reverse; intermittent)
25 °C max. inlet temp.
5.5 bar max. differential pressure (80 psi) at 25 °C (Forward)
6.9 bar max. differential pressure (100 psi) at 25 °C (Forward; intermittent)
80 psig max. inlet pressure
technique(s)
sterile filtration: suitable
L
37.6 cm (14.8 in.)
W
4.2 in.
cartridge nominal length
10 in. (25 cm)
diam.
10.7 in. (4.2 cm)
filtration area
1.0 m2
inlet to outlet W
15.2 cm (6.0 in.)
outlet connection diam.
1.5 in.
impurities
≤0.25 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
matrix
Millipore Express® SHC High Area
pore size
0.5/0.2 μm pore size
bubble point
≥4000 mbar (58 psig), air with water at 23 °C
fitting
1/4 in. drain/vent hose barb (with double O-ring seal)
inlet sanitary flange
outlet sanitary flange
(38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)
application(s)
sample preparation
General description
Packaging
Other Notes
Preparation Note
Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
Analysis Note
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
After sterilization and a controlled water flush of 21 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.
Legal Information
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