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Catalog No. KHGLS10FF1
Part No. KHGLS10FF1
Supplier Merck KGaA
Opticap® Sterile Multilayer XL10 Durapore® 0.45/0.22 µm 3/4 in. TC/TC
Net Price
472
Availability

4 weeks

PROPERTIES
  • Bacterial Endotoxins
    Aqueous extraction contains ≤0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
  • Bacterial Retention
    Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
  • Cartridge Nominal Length
    10 in. (25 cm)
  • Catalogue Number
    KHGLS10FF1
  • Chemistry
    Polyvinylidene Fluoride (PVDF)
  • Device Configuration
    Capsule
  • Device Material
    Polypropylene
  • Device Size
    10 in.
  • Diameter
    10.7 cm (4.2 in.)
  • European Pressure Equipment Directive
    EMD 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.
  • Filtration Area
    0.55 m²
  • Good Manufacturing Practices
    These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
  • Housing Material
    Polypropylene (PP)
  • Indirect Food Additive
    All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
  • Inlet Connection
    Sanitary Flange
  • Inlet Connection Diameter
    3/4 in.
  • Inlet to Outlet Width
    33.5 cm (13.2 in.)
  • Length
    10 in. (25 cm)
  • Material Package
    Double Easy-Open bag
  • Material Size
    1
  • Maximum Differential Pressure, bar (psid)
    Forward: 5.5 bar (80 psid) @ 25 °C; 1.05 bar (15 psid) @ 80 °C. Reverse: 3.5 bar (50 psid) @ 25 °C, intermittent
  • Maximum Inlet Pressure (psig)
    80 psig
  • 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
  • Maximum Inlet Temperature
    25 °C
  • Media
    Multilayer Durapore®
  • Non-Fiber Releasing
    This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
  • Outlet Connection
    Sanitary Flange
  • Outlet Connection Diameter
    3/4 in.
  • Oxidizable Substances
    Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1.5 L
  • Pore Size
    0.45 / 0.22 µm
  • Seal Material
    Lead O-ring: Silicone-coated EPDM, Outer O-ring: Silicone
  • Sterility
    Sterile
  • Sterilization
    3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
  • Support Material
    Polyester/Polyethylene
  • Trade Name
    Opticap®
  • USP Bacterial Endotoxins
    A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
  • Vent Cap Material
    Polypropylene (PP)
  • Wettability
    Hydrophilic
  • Width
    33.5 cm (13.2 in.)
DESCRIPTION
Genuine product
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