MCSL20S02

Durapore^® 5.0 µm，Millidisk^®小柱

Millidisk^® 20, filtration area 1000 cm², hydrophilic

• 别名: Millidisk Cartridge 20-stack 5.0 μm Hydrophilic
• 分類程式碼代碼: 23151806
• eCl@ss: 32031690

属性

• 材料: PVDF ; polysulfone ; polysulfone support; silicone seal
• 品質等級: 400
• 無菌: non-sterile
• 滅菌相容性: autoclavable compatible; steam-in-place compatible
• 產品線: Millidisk^® 20
• 特點: hydrophilic
• 製造商／商標名: Millidisk^®
• 參數: 0.35 bar max. differential pressure (5 psid) at 123 °C (Forward); 0.35 bar max. inlet pressure (5 psi) at 123 °C (Forward); 0.7 bar max. differential pressure (10 psid) at 25 °C (Reverse); 0.7 bar max. inlet pressure (10 psi) at 25 °C (Reverse); 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward); 1.7 bar max. inlet pressure (25 psi) at 80 °C (Forward); 4.1 bar max. differential pressure (60 psid) at 25 °C (Forward); 4.1 bar max. inlet pressure (60 psi) at 25 °C (Forward); 75 L/min flow rate at 2.8 bar (ΔP)
• 技術: prefiltration: suitable
• 過濾面積: 1000 cm²
• 雜質: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• 重量法萃取物: ≤5 mg/device
• 基質: Durapore^®
• 孔徑: 5.0 μm pore size
• 輸入: sample type liquid
• 起泡點: ≥138 mbar (2 psig), air with water at 23 °C
• 柱代碼: not applicable

说明

一般說明

Device Configuration: Cartridge

Stack Design: 20 Stak

包裝

Double Easy-Open bag

其他說明

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

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 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.

準備報告

Sterilization Method
5 SIP cycles of 60 min @ 135 °C; 5 autoclave cycles of 60 min @ 126 °C

This product was manufactured with a Durapore^® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

分析報告

使用 ≥200 mL 水冲洗后，将符合“USP 氧化物检测”要求

Gravimetric Extractables: using sterilized device after 24 hours in water at controlled room temperature

法律資訊

Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany

MILLIDISK is a registered trademark of Merck KGaA, Darmstadt, Germany