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KTGRA02HH3 Opticap Sterilizing Grade XL2 Aervent 0.2 µm 9/16 in. HB/HB

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KTGRA02HH3
3  Double Easy-Open bag
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Overview

Replacement Information
Description
Catalogue NumberKTGRA02HH3
ReplacesKTGP04HB3
Trade Name
  • Opticap®
DescriptionOpticap Sterilizing Grade XL2 Aervent 0.2 µm 9/16 in. HB/HB
References
Product Information
HS Code8421 29 90
Device ConfigurationCapsule
Connections, Inlet/Outlet14 mm (9/16 in.) Hose Barb
Connections, Vent/Drain1/4 in. Hose Barb with double O-ring Seal
Housing MaterialPolypropylene (PP)
Maximum Differential Pressure, bar (psid)Forward: 5.5 bar (80 psid) @ 25 °C; 1.0 bar (15 psid) @ 80 °C. Reverse: 4.1 bar (60 psid) @ 25 °C, intermittent
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
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.
Quality LevelMQ400
Applications
Biological Information
MediaAervent®
Sterilization30 autoclave cycles of 30 min @ 135 °C; not in-line steam sterilizable
Bacterial RetentionSamples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
WettabilityHydrophobic
Physicochemical Information
Pore Size0.2 µm
Inlet ConnectionHose Barb
Outlet ConnectionHose Barb
Bubble Point at 23 °C≥1100 mbar (16 psig) nitrogen with 70/30 % IPA/water
Gravimetric ExtractablesThe extractables level was equal to or less than 15 mg after 24 hours in a 70/30% IPA/water mixture at controlled room temperature.
HydroCorr≤0.12 mL/min @ 2.6 bar (38 psig)
Maximum Inlet Pressure (psig)80 psig
Maximum Inlet Temperature25 °C
Non-Fiber ReleasingThis product was manufactured with a PTFE membrane 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 Length5.5 in. (14.0 cm)
Length14.0 cm (5.5 in.)
Diameter8.4 cm (3.3 in.)
Filtration Area0.1 m²
Inlet to Outlet Width14.0 cm (5.5 in.)
Device Size2 in.
Inlet Connection Diameter9/16 in.
Outlet Connection Diameter9/16 in.
Materials Information
Chemistry
  • Polytetrafluoroethylene (PTFE)
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
Specifications
Global Trade Item Number
Catalogue Number GTIN
KTGRA02HH3 04053252264030

Documentation

Certificates of Quality

Title
OIpticap XL 2 Capsule Aervent Membrane C9EA98239
OPTI XL 2 Capsule Aervent Membrane C2MB16585
OPTICAP XL 2 Capsule Aervent Membrane C3JB47565
Opticap XL 2 Capsule Aervent Membrane C0KB04881
Opticap XL 2 Capsule Aervent Membrane C7JA47745
Opticap XL 2 Capsule Aervent Membrane C8AA17873
Opticap XL 2 Capsule Aervent Membrane C0PB12655
Opticap XL 2 Capsule Aervent Membrane C0PB49691
Opticap XL 2 Capsule Aervent Membrane C0PB62035
Opticap XL 2 Capsule Aervent Membrane C1BB41757

Technical Info

Title
Autoclaving Guidelines for Opticap® XL and XLT Disposable Capsule Filters
Bubble Point Test Method Using Aervent 0.2 µm Hydrophobic Membrane with 60/40 IPA

Data Sheet

Title
Sterilizing-Grade Aervent®Filters

User Guides

Title
Opticap® XL Capsules and Opticap® XLT Capsules