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物料
PVDF
质量水平
管理合规性
meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
无菌性
non-sterile
灭菌适用性
autoclavable compatible
steam-in-place compatible
产品线
Durapore®
特点
hydrophilic
制造商/商品名称
Durapore®
技术
bioburden reduction: suitable
长度
30 in.
宽度
2.7 in.
纯化柱标称长度
30 in. (75 cm)
过滤面积
2.07 m2
杂质
<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
重量萃取物
≤60 mg/cartridge
基质
Durapore®
孔径
0.45 μm
输入
sample type liquid
柱代码
Code 7 (2-226; O-rings w/locking-tabs)
相关类别
一般描述
Device Configuration: Cartridge
其他说明
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
制备说明
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
分析说明
Gravimetric Extractables: after 24 hours in water at controlled room temperature
法律信息
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
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