推荐产品
材料
PVDF membrane
polysulfone device
polysulfone support
品質等級
agency
certified by the ISO 9001:2015 (Quality Management Systems)
meets requirements for EP 2.6.14
meets requirements for JP 4.01
meets requirements for USP 85
無菌
irradiated
non-sterile (non-sterilized)
滅菌相容性
gamma compatible
產品線
Millipak® Final Fill 40
特點
hydrophilic
包裝
bag of 3 × double easy-open bag
參數
1.0 L/min flow rate at 0.69 bar
10 psi max. differential pressure (0.7 bar) at 25 °C (Reverse)
25 psi max. differential pressure (1.7 bar) at 25 °C (Forward)
50 psi max. differential pressure (3.5 bar) at 25 °C (Forward)
60 psi max. differential pressure (4.1 bar) at 25 °C (Forward)
60 psi max. inlet pressure (4.1 bar) at 25 °C
80 psi max. differential pressure (5.5 bar) at 25 °C (Forward)
80 psi max. inlet pressure (5.5 bar) at 25 °C
技術
sterile filtration: suitable
長度
3.4 in.
寬度
3.0 in.
過濾面積
200 cm2
雜質
<0.25 EU/mL bacterial endotoxins (LAL test)
基質
Durapore®
孔徑
0.22 μm pore size
起泡點
≥50 psi (3450 mbar), air with water at 23 °C
接頭
3/4 in. inlet connection
19 mm (3/4 in.) inlet/outlet connection (sanitary flange)
(19 mm (3/4 in.) Sanitary Flange Inlet and Outlet)
一般說明
包裝
準備報告
Device integrity and retention was maintained after 3 autoclave cycles of 90 minutes at 126 <nbsp/>°C. Devices can withstand a dose ? 40<nbsp/> kGy gamma exposure.
分析報告
其他說明
法律資訊
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相关内容
This page summarizes key considerations related to regulatory expectations for biomanufacturing including chemicals and polymeric materials. For chemicals, topics include nitrosamines and elemental impurities, and for polymeric materials such as filters and single-use assemblies, the focus is qualification and extractable and leachable testing.
This page summarizes key considerations related to regulatory expectations for biomanufacturing including chemicals and polymeric materials. For chemicals, topics include nitrosamines and elemental impurities, and for polymeric materials such as filters and single-use assemblies, the focus is qualification and extractable and leachable testing.
This page summarizes key considerations related to regulatory expectations for biomanufacturing including chemicals and polymeric materials. For chemicals, topics include nitrosamines and elemental impurities, and for polymeric materials such as filters and single-use assemblies, the focus is qualification and extractable and leachable testing.
This page summarizes key considerations related to regulatory expectations for biomanufacturing including chemicals and polymeric materials. For chemicals, topics include nitrosamines and elemental impurities, and for polymeric materials such as filters and single-use assemblies, the focus is qualification and extractable and leachable testing.
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