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KTGRA02NN3 Opticap XL 2 with Aervent - 2" 0.2um NPT/NPT 3pk

MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
KTGRA02NN3
3  Double Easy-Open bag
Purchase on Sigma-Aldrich

Overview

Replacement Information
Description
Catalogue NumberKTGRA02NN3
Trade Name
  • Opticap®
DescriptionOpticap XL 2 with Aervent - 2" 0.2um NPT/NPT 3pk
References
Product Information
Device ConfigurationCapsule
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) @ 25 °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.
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 ConnectionNPT
Outlet ConnectionNPT
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.
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 Length2 in. (5 cm)
Diameter8.4 cm (3.3 in.)
Filtration Area0.1 m²
Device Size2 in.
Inlet Connection Diameter1/4 in.
Outlet Connection Diameter1/4 in.
Materials Information
Chemistry
  • Polytetrafluoroethylene (PTFE)
Device Material
  • Polypropylene
Seal MaterialSilicone (SI)
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
KTGRA02NN3 04053252574795

Documentation

Certificates of Quality

Title
Opticap XL 2 Capsule Aervent Membrane C0CB25301R
Opticap XL 2 Capsule Aervent Membrane C7HA24965
Opticap XL 2 Capsule Aervent Membrane C7KA50804
Opticap XL 2 Capsule Aervent Membrane C8AA20589
Opticap XL 2 Capsule Aervent Membrane C8BA31470
Opticap XL 2 Capsule Aervent Membrane C9EA27702
Opticap XL 2 Capsule Aervent Membrane C9MA91602R
Opticap XL 2 Capsule Aervent Membrane C9PA13424R
Opticap XL 2 Capsule Aervent Membrane - C0AB81000R
Opticap XL 2 Capsule Aervent Membrane - C7CA84144
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User Guides

Title
Opticap® XL Capsules and Opticap® XLT Capsules