A part of Merck

KGW3A02TT3 | Opticap® XL2 Polysep® II 1.0/0.2 µm 1-1/2 in. TC/TC

3  Double Easy-Open bag
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      Replacement Information

      Key Spec Table

      Catalogue NumberKGW3A02TT3
      Trade Name
      • Opticap®
      DescriptionOpticap® XL2 Polysep® II 1.0/0.2 µm 1-1/2 in. TC/TC
      Product Information
      FormatDouble Layer
      Device ConfigurationCapsule
      Connections, Inlet/Outlet38 mm (1-1/2 in.) Sanitary Flange
      Housing MaterialPolypropylene (PP)
      Maximum Differential Pressure, bar (psid)3.5 bar (50 psid) @ 25 °C
      Maximum Inlet Pressure, bar (psi)5.5 bar (80 psi) @ 23 °C; 2.75 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C
      European Pressure Equipment DirectiveEMD 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.
      Good Manufacturing PracticesThese products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
      Prefilter MaterialBorosilicate Glass Fiber (BGF)
      Biological Information
      Bacterial EndotoxinsAqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
      MediaPolysep™ II
      Sterilization3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable
      Physicochemical Information
      Inlet ConnectionSanitary Flange
      Outlet ConnectionSanitary Flange
      Gravimetric ExtractablesThe extractables level was equal to or less than 45 mg per capsule after a 600 mL flush and 24 hours in water at controlled room temperature.
      Indirect Food AdditiveAll component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
      Maximum Inlet Pressure (psig)80 psig
      Maximum Inlet Temperature25 °C
      Non-Fiber ReleasingThis 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).
      USP Bacterial EndotoxinsA sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
      Cartridge Nominal Length2 in. (5 cm)
      Length14.2 cm (5.6 in.)
      Diameter14.5 cm (5.7 in.)
      Filtration Area0.06 m²
      Inlet to Outlet Width14.2 cm (5.6 in.)
      Device Size2 in.
      Inlet Connection Diameter1-1/2 in.
      Nominal Pore Size1.0 / 0.2 µm
      Outlet Connection Diameter1-1/2 in.
      Materials Information
      • Mixed Cellulose Esters (MCE)
      Device Material
      • Polypropylene
      Seal MaterialSilicone (SI)
      Support MaterialPolypropylene
      Vent Cap MaterialPolypropylene (PP)
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Packaging Information
      Material Size3
      Material PackageDouble Easy-Open bag
      Transport Information
      Supplemental Information
      Oxidizable SubstancesWill meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L




      Safety Data Sheet (SDS) 

      Certificates of Quality

      Optica[ XL 2 Capsule Polysep II Media C5CA85736
      Opticap XL 2 Capsule Polysep II Media C6PA36837
      Opticap XL 2 Capsule Polysep II Media C5CA74804
      Opticap XL 2 Capsule Polysep II Media - C2NA93147
      Opticap XL 2 Capsule Polysep II Media - C2PA08733
      Opticap XL 2 Capsule Polysep II Media - C2SA19517
      Opticap XL 2 Capsule Polysep II Media - C2SA20630
      Opticap XL 2 Capsule Polysep II Media - C3AA41184
      Opticap XL 2 Capsule Polysep II Media - C3EA09036
      Opticap XL 2 Capsule Polysep II Media - C3JA77440