产品名称
Durapore® 0.22 µm, Optiseal® 滤芯, OptiSeal® 4 in., filtration area 0.18 m2, matrix Durapore®
material
PVDF
polypropylene
polypropylene support
silicone seal
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
≤5 mL/min air diffusion at 2.75 bar (40 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 850 mbar (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
0.22 μm
input
sample type liquid
bubble point
≥3450 mbar (50 psig), air with water at 23 °C
cartridge code
not applicable
Quality Level
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Analysis Note
使用ASTM® F838方法,对样品进行最小保留的缺陷短波单孢菌挑战浓度为 1 × 10⁷ CFU/cm² 的定量保留。
General description
Other Notes
- 生物截留:微生物
- 作用机制:过滤(体积排阻)
- 应用:生物处理
- 预期用途:减少或去除微生物/生物负荷
- 使用说明:参见《Durapore® 滤膜过滤器润湿说明》用户手册
- 存储声明:干燥储存
- 处置声明:根据国家、省市和当地适用法规处置。
Packaging
Preparation Note
30 SIP 循环 30 分钟 @ 135 °C;10 个 30 分钟 @ 126 °C 的高压蒸汽循环
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