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KGW3A2TTT1 Opticap® XLT20 Polysep® II 1.0/0.2 µm 1-1/2 in. TC

KGW3A2TTT1
1  Double Easy-Open bag
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Replacement Information
Description
Catalogue NumberKGW3A2TTT1
Trade Name
  • Opticap®
DescriptionOpticap® XLT20 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 290 mg per capsule after a 10 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 Length20 in. (50 cm)
Length62.5 cm (24.6 in.)
Filtration Area0.92 m²
Inlet to Outlet Width15.2 cm (6.0 in.)
Device Size20 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 ≥10 L
Global Trade Item Number
Katalogové číslo GTIN
KGW3A2TTT1 04053252609275

Documentation

Opticap® XLT20 Polysep® II 1.0/0.2 µm 1-1/2 in. TC MSDS

Title

Safety Data Sheet (SDS) 

Certificates of Quality

Title
OPTICAP XLT 20 capsule Polysep II media C3MB59996
Opticap XL 20 Capsule Polysep ii Media C9EA37471
Opticap XLT 20 Capsule Polysep II Media - C7CA82588
Opticap XLT 20 Capsule Pollysep II Media C8JA78842
Opticap XLT 20 Capsule Polysep 11 Media C4EB20621
Opticap XLT 20 Capsule Polysep II Media C8DA58231
Opticap XLT 20 Capsule Polysep II Media C7PA85145
Opticap XLT 20 Capsule Polysep II Media C4EB32078
Opticap XLT 20 Capsule Polysep II Media C7DA94159
Opticap XLT 20 Capsule Polysep II Media C7SA04517

Technical Info

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

User Guides

Title
Opticap® XL Capsules and Opticap® XLT Capsules