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KTGRA02TH3 Opticap XL 2 with Aervent - 2" 0.2um TC/HB 3pk

Opticap XL 2 with Aervent - 2" 0.2um TC/HB 3pk: MSDS (material safety data sheet) o SDS, certificato d’analisi (CoA) e certificato di qualità (CoQ), dossier, brochure e altri documenti disponibili.
KTGRA02TH3
3  Double Easy-Open bag
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Panoramica

Replacement Information
Description
Catalogue NumberKTGRA02TH3
Trade Name
  • Opticap®
DescriptionOpticap XL 2 with Aervent - 2" 0.2um TC/HB 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®
Sterilization3 autoclave cycles of 60 min @ 123 °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 ConnectionSanitary Flange
Outlet ConnectionHose Barb
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 Diameter1-1/2 in.
Outlet Connection Diameter9/16 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
Numero di catalogo GTIN
KTGRA02TH3 04053252559181

Documentation

Certificati di Qualità

Titolo
OPTI XL 2 Capsule Aervent Membrane C2JB89064
Opticap XL 2 CCapsule Aervent Membrane C7CA91967
Opticap XL 2 Capsule Aervent Membrane C7DA01312
Opticap XL 2 Capsule Aervent Membrane C7DA06964
Opticap XL 2 Capsule Aervent Membrane C7PA89807
Opticap XL 2 Capsule Aervent Membrane C0EB22927R
Opticap XL 2 Capsule Aervent Membrane C0KB04882
Opticap XL 2 Capsule Aervent Membrane C0PB12667
Opticap XL 2 Capsule Aervent Membrane C3DB99485
Opticap XL 2 Capsule Aervent Membrane C7NA70175
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Manuali d'uso

Titolo
Opticap® XL Capsules and Opticap® XLT Capsules