CVDR02TP3

Durapore 筒式过滤器，带预滤器 20 in.0.65 µm 0 号

pore size 0.65 μm, cartridge nominal length 20 in. (50 cm), Code 0 (2-222; O-rings)

• 别名: Durapore^®（带预滤器）0.65 µm，小柱
• UNSPSC代码: 23151806
• eCl@ss: 32031690

属性

• 物料: PVDF ; mixed cellulose esters (MCE) prefilter; polypropylene ; polypropylene support; silicone seal
• 质量水平: 400
• 管理合规性: meets EU framework regulation [1935/2004/EC] (all component materials; regarding materials and articles intended to contact food); meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• 无菌性: non-sterile
• 灭菌适用性: autoclavable compatible; steam-in-place compatible
• 产品线: Durapore^®
• 特点: hydrophilic
• 制造商/商品名称: Durapore^®
• 参数: ≤20 mL/min air diffusion at 620 mbar (9 psig) and 23 °C (in water); 0.35 bar max. differential pressure (5 psid) at 121 °C (Forward); 0.35 bar max. inlet pressure (5 psi) at 121 °C (Forward); 1.7 bar max. differential pressure (25 psid) 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 25 °C (Reverse); 1.7 bar max. inlet pressure (25 psi) at 80 °C (Forward); 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward); 5.5 bar max. inlet pressure (80 psi) at 25 °C (Forward)
• 技术: prefiltration: suitable
• 长度: 20 in.
• 宽度: 2.7 in.
• 纯化柱标称长度: 20 in. (50 cm)
• 直径: 6.9 cm (2.7 in.)
• 过滤面积: 1.38 m²
• 杂质: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• 重量萃取物: ≤90 mg/cartridge
• 基质: Durapore^® (w/Prefilter)
• 孔径: 0.65 μm pore size
• 输入: sample type liquid
• 泡点: ≥965 mbar (14 psig), air with water at 23 °C
• 柱代码: Code 0 (2-222; O-rings)

说明

一般描述

Device Configuration: Cartridge

包装

Double Easy-Open bag

其他说明

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.

制备说明

Sterilization Method
8 SIP cycles of 30 min or 8 autoclave cycles of 60 min @ 121 °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).

分析说明

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

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L

法律信息

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

安全信息

• 储存分类代码: 4.1B - Flammable solid hazardous materials
• WGK: WGK 3