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Catalog No. KVGLA3THH1
Part No. KVGLA3THH1
Supplier Merck KGaA
Opticap® XLT30 Durapore® 0.22 µm 5/8 in. HB/HB
Net Price
1154
Availability

4 weeks

PROPERTIES
  • Bacterial Endotoxins
    Aqueous extraction contains ≤0.5 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
    30 in. (75 cm)
  • Catalogue Number
    KVGLA3THH1
  • Chemistry
    Polyvinylidene Fluoride (PVDF)
  • Device Configuration
    Capsule
  • Device Material
    Polypropylene
  • Device Size
    30 in.
  • Diameter
    10.7 cm (4.2 in.)
  • Filtration Area
    2.1 m²
  • Good Manufacturing Practices
    These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
  • Gravimetric Extractables
    The extractables level was equal to or less than 75 mg per capsule after 24 hours in water at controlled room temperature.
  • 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
    Hose Barb
  • Inlet Connection Diameter
    5/8 in.
  • Inlet to Outlet Width
    19.8 cm (7.8 in.)
  • Length
    30 in. (75 cm)
  • Material Package
    Double Easy-Open bag
  • Material Size
    1
  • Maximum Differential Pressure, bar (psid)
    Forward: 5.5 bar (80 psid) @ 25 °C; 1.7 bar (25 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; 2.8 bar (40 psi) @ 60 °C; 1.0 bar (15 psi) @ 80 °C
  • Maximum Inlet Temperature
    25 °C
  • Media
    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
    Hose Barb
  • Outlet Connection Diameter
    5/8 in.
  • Oxidizable Substances
    Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥3 L
  • Pore Size
    0.22 µm
  • Seal Material
    Silicone (SI)
  • Sterility
    Other
  • Sterilization
    3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable
  • Support Material
    Polypropylene
  • Trade Name
    Opticap®
  • USP Bacterial Endotoxins
    A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
  • Vent Cap Material
    Polypropylene (PP)
  • Wettability
    Hydrophilic
  • Width
    19.8 cm (7.8 in.)
DESCRIPTION
Genuine product
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