产品名称
Durapore® 0.1 µm,小柱,
Quality Level
material
PVDF , polypropylene , polypropylene support, silicone seal
reg. compliance
meets EU framework regulation [1935/2004/EC] (all component materials; regarding materials and articles intended to contact food), 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
Durapore®
feature
hydrophilic
manufacturer/tradename
Durapore®
parameter
≤10 mL/min air diffusion at 3.9 bar (56 psig) and 23 °C (in water), 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), 3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse), 3.5 bar max. inlet pressure (50 psi) at 25 °C (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), 7.5 L/min flow rate at 700 mbar (ΔP)
technique(s)
sterile filtration: suitable
L
5 in.
W
2.7 in.
cartridge nominal length
5 in. (12.5 cm)
diam.
6.9 cm (2.7 in.)
filtration area
0.34 m2
impurities
≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction), <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
matrix
Durapore®
pore size
0.1 μm pore size
input
sample type liquid
bubble point
≥4830 mbar (70 psig), air with water at 23 °C
cartridge code
Code 7 (2-226; O-rings w/locking-tabs)
General description
Packaging
Preparation Note
在135 °C下进行30次30分钟的SIP循环;在126 °C下进行30次60分钟的高压灭菌循环
Analysis Note
按ASTM® F838方法进行细菌挑战,样品可截留1 x 10⁷ CFU/cm²以上浓度的缺陷短波单孢菌。
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。
Legal Information
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全球贸易项目编号
| 货号 | GTIN |
|---|---|
| CVVL75S01 | 04053252393860 |