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品質等級
法律遵循
meets FDA 21 CFR 177-182 (all component materials)
無菌
non-sterile
滅菌相容性
autoclavable compatible
steam-in-place compatible
產品線
Polysep™
特點
hydrophilic
製造商/商標名
Polysep™
參數
3.5 bar max. differential pressure (50 psid) at 25 °C
3.5 bar max. inlet pressure (50 psi) at 25 °C
技術
prefiltration: suitable
長度
40 in.
寬度
2.7 in.
柱標稱長度
100 cm (40 in.)
過濾器直徑
7.1 cm (2.8 in.)
過濾器過濾面積
1.84 m2
雜質
≤0.5 EU/mL bacterial endotoxins (LAL test, aqueous extraction )
<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction )
基質
Polysep™ II
pore size
1.0/0.5 μm nominal pore size
1.0/0.5 μm pore size
柱代碼
Code 7
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一般說明
Device Configuration: Cartridge
特點和優勢
Double Layer
包裝
Double Easy-Open bag
準備報告
Non-Fiber Releasing: This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21CFR210.3(b)(6).
Sterilization Method: 10 autoclave cycles or SIP for 30 min at 121 °C
分析報告
Gravimetric Extractables: the extractables level was equal to or less than 140 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 20 L
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 20 L
其他說明
Directions for Use
- Organism Retention: Microorganism
- Mode of Action: Filtration (size exclusion)
- Application: BioProcessing
- Intended Use: Reduction or removal of microorganism/bioburden
- Instructions for Use: Please refer first page of Visual Inspection Guide and introduction section of Mixed cellulose esters Tech Brief
- Storage Statement: Please refer Mixed cellulose esters Tech Brief
- Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
法律資訊
Polysep is a trademark of Sigma-Aldrich Co. LLC
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