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品質等級
法律遵循
FDA 21CFR177-182 (all component materials)
無菌
non-sterile
滅菌相容性
gamma compatible
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 3.9 bar (56 psig) and 23 °C (in water)
1 bar max. inlet pressure (15 psi) at 80 °C
2.1 bar max. differential pressure (30 psid) at 4-40 °C (Reverse:)
2.8 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
4.1 bar max. differential pressure (60 psid) at 25 °C (Forward:)
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure
技術
bioburden reduction: suitable
寬度
6.0 in.
柱標稱長度
34.3 in. (87.1 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
1.86 m2
入口接頭直徑
1-1/2 in.
入口到出口寬度
87.1 cm (34.3 in.)
出口接頭直徑
1-1/2 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
Durapore®
孔徑
0.45 μm pore size
起泡點
≥1930 mbar (28 psig), air with water at 23 °C
接頭
1/4 in. fitting (vent/drain hose barb with double O-ring seal)
(38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)
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一般說明
準備報告
Gamma compatible to 40 kGy. 3 autoclave cycles of 60min at 3°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 installation section of Opticap® XL Capsules and Opticap® XLT Capsules 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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分析證明 (COA)
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