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材料
PVDF
polysulfone
polysulfone support
品質等級
無菌
non-sterile
特點
hydrophilic
參數
10 psi max. differential pressure (0.7 bar) at 25 °C (Reverse)
3.0 L/min flow rate at 0.69 bar
80 psi max. differential pressure (5.5 bar) at 25 °C (Forward)
80 psi max. inlet pressure (5.5 bar) at 25 °C
過濾面積
500 cm2
入口接頭直徑
1 1/2 in.
出口接頭直徑
1-1/2 in.
尺寸
100 L
雜質
<0.25 EU/mL Aqueous extraction (LAL test, meeting requirements of USP <85>, EP 2.6.14 and JP 4.01.)
基質
Durapore®
孔徑
0.45 μm
起泡點
≥26 psi (1790 mbar), air with water
接頭
inlet sanitary flange
outlet sanitary flange
38 mm (1 1/2 in.) sanitary flange drain/vent
適合性
suitable for endotoxin
一般說明
Aqueous extraction contains < 0.25<nbsp/> EU/mL per device as determined using the Limulus Amebocyte Lysate (LAL) test, meeting requirements of USP <85>, EP 2.6.14 and JP 4.01.
Device integrity and retention was maintained after 3 autoclave cycles of 90 minutes at 126 °C. Devices can withstand a dose ? 40 kGy gamma exposure.
包裝
Double Easy-Open bag
法律資訊
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPAK is a registered trademark of Merck KGaA, Darmstadt, Germany
免責聲明
These products are manufactured in a facility which is certified to ISO 9001:2015 Quality Management Systems.
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