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Bacterial Endotoxins
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
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Catalogue Number
SVPVA25NB9
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Chemistry
Modified Polyvinylidene Fluoride (Modified PVDF)
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Device Configuration
Validation Kit
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Device Material
PVDF
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Filtration Area
3.5 cm²
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Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
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Inlet Connection
Female Luer Lok
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Key Applications
Protein Purification
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Length
2.2 cm (0.87 in.)
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Material Size
9
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Maximum Differential Pressure, bar (psid)
Forward: 5.5 bar (80 psid). Reverse: 0.7 bar (10 psid)
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Maximum Inlet Pressure, bar (psi)
5.5 bar (80 psi) @ 23 °C
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Media
Viresolve® NFP
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Non-Fiber Releasing
This product was manufactured with a Viresolve® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
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Outlet Connection
Male Luer Slip
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Process Volume
70 mL
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Seal Material
Silicone (SI)
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Sterilization
Water wet filter for 5 min @ 3.4 bar (50 psi); liquid cycle, slow exhaust @ 123 °C maximum 60 min
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Trade Name
OptiScale®
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USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
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Volume
70 mL
+852-3069 6950
sales@gugent.com.hk
