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材料
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polypropylene filter
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silicone seal
品質等級
法律遵循
FDA 21CFR177-182 (all component materials)
無菌
sterile; irradiated
產品線
Opticap® XLT 30
特點
hydrophilic
製造商/商標名
Opticap®
參數
≤45.0 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water)
1 bar max. inlet pressure (15 psi) at 80 °C
1.05 bar max. differential pressure (15 psid) at 80 °C (Forward:)
2.75 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse; intermittent)
5.5 bar max. differential pressure (80 psid) at 25 °C (Forward:)
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure
技術
sterile filtration: suitable
柱標稱長度
30 in. (75 cm)
設備長度
87.1 cm (34.3 in.)
設備尺寸
30 in.
過濾器直徑
4.2 in. (10.7 cm)
過濾器過濾面積
0.1 m2
入口接頭直徑
5/8 in.
入口到出口寬度
19.8 cm (7.8 in.)
出口接頭直徑
5/8 in.
雜質
≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction)
<0.25 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)
基質
Multilayer Durapore®
pore size
0.45/0.22 μm pore size
起泡點
≥3450 mbar (50 psig), air with water at 23 °C
接頭
1/4 in. fitting (vent/drain hose barb with double O-ring seal)
(16 mm (5?8 in.) Hose Barb Inlet and Outlet)
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一般說明
包裝
準備報告
3 autoclave cycles of 60min at 126°C; not in-line steam sterilizable
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21CFR210.3(b)(6).
分析報告
其他說明
- Organism Retention: Microorganism
- Mode of Action: Filtration (size exclusion)
- Application: BioProcessing
- Intended Use: Reduction or removal of microorganism/bioburden
- Instructions for Use: Please refer Wetting Instructions for Filter Units with Durapore® Membrane user guide
- Storage Statement: Store in dry location
- Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations
法律資訊
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