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Opticap XL Capsule Filter

Description:
Opticap XL5 Milligard Low Protein Binding 1.2/0.5 µm 1-1/2 in. TC/TC
Trade Name:
Opticap
Qty/Pk:
Key Applications:
Laboratory Filtration
Filter Grade:
Low Protein Binding Milligard Media, 1.2/0.5 µm
Maximum Inlet Temperature, °C:
Outlet Connection Diameter (in):
1-1/2
Inlet Connection Diameter (in):
1-1/2
Outlet Connection:
Sanitary Flange
Maximum Inlet Pressure, bar (psi):
5.5 (80) @ 23 °C; 2.75 (40) @ 60 °C; 1.0 (15) @ 80 °C
Maximum Inlet Pressure (psig):
Filtration Area, m²:
Maximum Differential Pressure, bar (psid):
3.5 (50) @ 25 °C
Diameter, cm (in):
14.5 (5.7)
Inlet Connection:
Sanitary Flange
Oxidizable Substances:
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L
Cartridge Nominal Length, in (cm):
5 (12.5)
Pore Size (µm):
1.2 / 0.5
Sterilization:
3 autoclave cycles of 30 min @ 121 °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.
Nominal Pore Size (µm):
1.2 / 0.5
Gravimetric Extractables:
The extractables level was equal to or less than 145 mg per capsule after a 2 L flush and 24 hours in water at controlled room temperature.
Product Name:
Opticap XL Capsule Filter
Non-Fiber Releasing:
This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Filtration Area, cm²:
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:
38 mm (1-1/2 in.) Sanitary Flange
Length, cm (in):
21.6 (8.5)
Configuration:
Capsule
Chemistry:
Mixed Cellulose Esters
Media:
Milligard
Format:
Double Layer
Support Material:
Polyester
Inlet to Outlet Width, cm (in):
21.6 (8.5)
Packaging:
Double Easy-Open bag
Seal Material:
Silicone
Device Size (in):

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