CHVE71TF3

ミリポアエクスプレス（Millipore Express）^®SHRP、カートリッジ

with prefilter, cartridge nominal length 10 in. (25 cm), filter diam. 2.7 in. (6.9 cm), Code 7

• UNSPSCコード: 23151806

特性

• 物質: polypropylene support; seal (Fluorocarbon rubber)
• 品質水準: 400
• 法規制遵守: meets FDA 21 CFR 177-182 (all component materials)
• 無菌性: non-sterile
• 滅菌適合性: autoclavable compatible; steam-in-place compatible
• 製品種目: Millipore Express^®
• 特徴: hydrophilic; with prefilter
• メーカー／製品名: Millipore Express^®
• パラメーター: ≤27.1 mL/min air diffusion at 3.45 bar (50 psig) (in water); 0.07 bar max. differential pressure (1 psi) at 135 °C (Reverse); 0.35 bar max. differential pressure (5 psi) at 135 °C (Forward); 1.7 bar max. differential pressure (25 psi) at 80 °C (Forward); 1000 mbar max. differential pressure (15 psi) at 135 °C (Forward); 1700 mbar max. differential pressure (25 psi) at 80 °C (Forward); 2.07 bar max. differential pressure (30 psi) at 25 °C (Reverse); 2100 mbar max. differential pressure (30 psi) at 25 °C (Reverse); 6.9 bar max. differential pressure (100 psi) at 25 °C (Forward); 69 mbar max. differential pressure (<1.0 psi) at 135 °C (Reverse); 6900 mbar max. differential pressure (100 psi) at 25 °C (Forward)
• テクニック: sterile filtration: suitable
• L: 10 in.
• W: 2.7 in.
• カートリッジの長さ（公称）: 10 in. (25 cm)
• フィルタ直径: 2.7 in. (6.9 cm)
• フィルタサイズ: 10 in.
• ろ過面積: 0.48 m²
• 不純物: ≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• マトリックス: Millipore Express^® SHR (w/Prefilter)
• pore size: 0.5/0.1 μm pore size
• 泡立ち点: ≥2586 mbar (37.5 psig), nitrogen with 70/30% IPA/water
• カートリッジコード: Code 7

詳細

詳細

Cartridge Type: Liquid

Device Configuration: Cartridge

包装

Double Easy-Open bag

調製ノート

Sterilization Method: 25 forward or 22 forward and 3 reverse SIP cycles of 30 min at 135 °C, or 3 forward cycles, 30 min., 135 °C at ≤1000 mbar (15 psid); 25 autoclave cycles of 60 min at 126 °C

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

アナリシスノート

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L

TOC/Conductivity: After sterilization and a controlled water flush of 20 L, samples exhibited <500 ppb TOC per USP 643 and <1.3 μS/cm per USP 645 at 25 °C.

Bacterial Retention: Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM^® F838 methodology.

その他情報

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 of Filters with MILLIPORE EXPRESS^® Membrane user guide
• Storage Statement: Please refer Filters with MILLIPORE EXPRESS^® Membrane user guide
• 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.

法的情報

ASTM is a registered trademark of American Society for Testing and Materials

MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany