OptiScale-25 with Viresolve NFP Validation Kit, 3 membrane lots
Net Price
Special offer
Availability
4 weeks
PROPERTIES
Bacterial Endotoxins
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Catalogue Number
SVPVA25NB9
Chemistry
Modified Polyvinylidene Fluoride (Modified PVDF)
Device Configuration
Validation Kit
Device Material
PVDF
Filtration Area
3.5 cm²
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Inlet Connection
Female Luer Lok
Key Applications
Protein Purification
Length
2.2 cm (0.87 in.)
Material Size
9
Maximum Differential Pressure, bar (psid)
Forward: 5.5 bar (80 psid). Reverse: 0.7 bar (10 psid)
Maximum Inlet Pressure, bar (psi)
5.5 bar (80 psi) @ 23 °C
Media
Viresolve® NFP
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).
Outlet Connection
Male Luer Slip
Process Volume
70 mL
Seal Material
Silicone (SI)
Sterilization
Water wet filter for 5 min @ 3.4 bar (50 psi); liquid cycle, slow exhaust @ 123 °C maximum 60 min
Trade Name
OptiScale®
USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
+852-3069 6950
sales@gugent.com.hk
