LAVL04TP6
Durapore® 0.1 µm, Optiseal® Cartridge
OptiSeal® 4 in., filtration area 0.18 m2, matrix Durapore®
Sinónimos:
Optiseal Durapore Cartridge Filter 0.1 μm
About This Item
Productos recomendados
material
PVDF
polypropylene
polypropylene support
silicone seal
Quality Level
reg. compliance
meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
sterility
non-sterile
sterilization compatibility
autoclavable compatible
steam-in-place compatible
product line
OptiSeal® 4 in.
feature
hydrophilic
manufacturer/tradename
OptiSeal®
parameter
≤7 mL/min air diffusion at 3.9 bar (56 psig) and 23 °C (in water)
0.35 bar max. differential pressure (5 psid) at 121 °C (Forward)
0.35 bar max. inlet pressure (5 psi) at 135 °C (Forward)
15 L/min flow rate at 2 bar (ΔP)
3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse)
3.5 bar max. differential pressure (50 psid) at 80 °C (Forward)
3.5 bar max. inlet pressure (50 psi) at 25 °C (Reverse)
3.5 bar max. inlet pressure (50 psi) at 80 °C (Forward)
5.5 bar max. differential pressure (80 psid) at 25 °C (Forward)
5.5 bar max. inlet pressure (80 psi) at 25 °C (Forward)
technique(s)
sterile filtration: suitable
L
4 in.
cartridge nominal length
4 in. (10 cm)
filtration area
0.18 m2
impurities
≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
gravimetric extractables
≤10 mg/cartridge
matrix
Durapore®
pore size
0.1 μm
input
sample type liquid
bubble point
≥4830 mbar (70 psig), air with water at 23 °C
cartridge code
not applicable
General description
Packaging
Other Notes
- Organism Retention: Microorganism
- Mode of Action: Filtration (size exclusion)
- Application: BioProcessing
- Intended Use: Reduction or removal of microorganism/bioburden
- Instructions for Use: Please refer Wetting Instructions for Filter Units with Durapore® Membrane user guide
- Storage Statement: Store in dry location
- Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.
Preparation Note
30 SIP cycles of 30 min @ 135 °C; 10 autoclave cycles of 30 min @ 126 °C
Analysis Note
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
Legal Information
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