产品名称
Aervent® 0.2 µm, Optiseal® 小柱, pore size 0.2 μm, OptiSeal® 4 in., filtration area 0.05 m2, matrix Aervent®
material
PTFE
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
hydrophobic
manufacturer/tradename
OptiSeal®
parameter
0.35 bar max. differential pressure (5 psid) at 135 °C (Forward)
0.35 bar max. inlet pressure (5 psi) at 135 °C (Forward)
1.7 bar max. differential pressure (25 psid) at 80 °C (Forward)
1.7 bar max. inlet pressure (25 psi) at 80 °C (Forward)
4.1 bar max. differential pressure (60 psid) (Reverse)
4.1 bar max. inlet pressure (60 psi) (Reverse;)
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)
gas filtration: suitable
cartridge nominal length
1 in. (2.5 cm)
filtration area
0.05 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
≤2.5 mg/cartridge
matrix
Aervent®
pore size
0.2 μm pore size
input
sample type liquid
bubble point
≥1100 mbar (16 psig), nitrogen with 70/30% IPA/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:参见蒸汽灭菌&《完整性测试程序指南》和《目视检查指南》第一页
- 储存声明: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 min、135 °C条件下80次(40 次正向/40次反向)在线灭菌
Legal Information
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