Opticap® Sterile XLT10 Durapore® 0.45 µm 5/8" HB/HB without gauge port
Net Price
298
Availability
4 weeks
PROPERTIES
Bacterial Endotoxins
Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Cartridge Nominal Length
14.8 in. (37.6 cm)
Catalogue Number
KPHLS1THH1
Chemistry
Polyvinylidene Fluoride (PVDF)
Device Configuration
Capsule
Device Material
Polypropylene
Device Size
10 in.
Diameter
10.7 cm (4.2 in.)
Filtration Area
0.62 m²
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Gravimetric Extractables
The extractables level was equal to or less than 25 mg per capsule after 24 hours in water at controlled room temperature.
Housing Material
Polypropylene (PP)
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
Inlet Connection
Hose Barb
Inlet Connection Diameter
5/8 in.
Inlet to Outlet Width
37.6 cm (14.8 in.)
Length
14.8 in. (37.6 cm)
Material Size
1
Maximum Differential Pressure, bar (psid)
Forward: 4.1 bar (60 psid) @25 ˚C. Reverse: 2.1 bar (30 psid) @ 4-40 °C
Maximum Inlet Pressure (psig)
80 psig
Maximum Inlet Pressure, bar (psi)
5.5 bar (80 psi) @ 23 °C; 2.8 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C
Maximum Inlet Temperature
25 °C
Media
Durapore®
Outlet Connection
Hose Barb
Outlet Connection Diameter
5/8 in.
Oxidizable Substances
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1500 mL
Pore Size
0.45 µm
Seal Material
Lead O-ring: Silicone-coated EPDM, Outer O-ring: Silicone
Sterility
Sterile
Sterilization
Minimum sterilization up to 25 kGy. 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
Support Material
Polyester/Polyethylene
Trade Name
Opticap®
USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
Vent Cap Material
Polypropylene (PP)
Wettability
Hydrophilic
Width
37.6 cm (14.8 in.)
DESCRIPTION
Prefiltration / Bioburden reduction in single use assemblies Bioburden reduction before final sterilization Process protection of intermediate consumables esp. in Plasma / Vaccine / r-Protein