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KGW3A1TTT1 Opticap® XLT10 Polysep® II 1.0/0.2 µm 1-1/2 in. TC

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KGW3A1TTT1
1  Double Easy-Open bag
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Overview

Replacement Information
Description
Catalogue NumberKGW3A1TTT1
Trade Name
  • Opticap®
DescriptionOpticap® XLT10 Polysep® II 1.0/0.2 µm 1-1/2 in. TC
References
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)
T-line/Gauge PortT-line
Quality LevelMQ400
Applications
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
Pore Size1.0 / 0.2 µm
Inlet ConnectionSanitary Flange
Outlet ConnectionSanitary Flange
Gravimetric ExtractablesThe extractables level was equal to or less than 145 mg per capsule after a 5 L 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.
Dimensions
Cartridge Nominal Length10 in. (25 cm)
Length37.6 cm (14.8 in.)
Filtration Area0.46 m²
Inlet to Outlet Width15.2 cm (6.0 in.)
Device Size10 in.
Inlet Connection Diameter1-1/2 in.
Nominal Pore Size1.0 / 0.2 µm
Outlet Connection Diameter1-1/2 in.
Materials Information
Chemistry
  • 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 Size1
Material PackageDouble Easy-Open bag
Transport Information
Supplemental Information
Specifications
Oxidizable SubstancesWill meet the USP Oxidizable Substances Test requirements after a water flush of ≥5 L
Global Trade Item Number
Catalog Number GTIN
KGW3A1TTT1 04053252342936

Documentation

Opticap® XLT10 Polysep® II 1.0/0.2 µm 1-1/2 in. TC SDS

Title

Safety Data Sheet (SDS) 

Certificates of Quality

Title
OPTICAP XLT 20 capsule Polysep II media C4EB24427
Opticap XL 10 Capsule Polysep II Media C1JB22738
Opticap XLT 10 Capsule Polysep II Media C0JB87269
Opticap XLT 10 Capsule Polysep II Media C1AB41773
Opticap XLT 10 Capsule Polysep II Media C3DB08844
Opticap XLT 10 Capsule Polysep II Media C7PA89826
Opticap XLT 10 Capsule Polysep II Media C8NA15526
Opticap XLT 10 Capsule Polysep II Media C9HA45741
Opticap XLT 10 Capsule Polysep II Media C9NA07382
Opticap XLT 10 Capsule Polysep II Media - C7HA21455

Technical Info

Title
Autoclaving Guidelines for Opticap® XL and XLT Disposable Capsule Filters

User Guides

Title
Opticap® XL Capsules and Opticap® XLT Capsules