CVVL51TP3

Durapore^® 0.1 µm、カートリッジ

pore size 0.1 μm, cartridge nominal length 10 in. (25 cm), Code 5 (2-222; O-rings and spear)

• 別名: Durapore Cartridge Filter 10 in. 0.1 μm Code 5
• UNSPSCコード: 23151806
• eCl@ss: 32031690

特性

• 物質: PVDF ; polypropylene ; polypropylene support; silicone seal
• 品質水準: 400
• 法規制遵守: 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)
• 無菌性: non-sterile
• 滅菌適合性: autoclavable compatible; steam-in-place compatible
• 製品種目: Durapore^®
• 特徴: hydrophilic
• メーカー／製品名: Durapore^®
• パラメーター: ≤20 mL/min air diffusion at 3.9 bar (56 psig) and 23 °C (in water); 0.35 bar max. differential pressure (5 psid) at 135 °C (Forward); 0.35 bar max. inlet pressure (5 psi) at 135 °C (Forward); 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward); 1.7 bar max. inlet pressure (25 psi) at 80 °C (Forward); 15 L/min flow rate at 700 mbar (ΔP); 3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse); 3.5 bar max. inlet pressure (50 psi) at 25 °C (Reverse); 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward); 5.5 bar max. inlet pressure (80 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)
• 直径: 6.9 cm (2.7 in.)
• ろ過面積: 0.69 m²
• 不純物: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• マトリックス: Durapore^®
• ポアサイズ: 0.1 μm pore size
• 入力: sample type liquid
• 泡立ち点: ≥4830 mbar (70 psig), air with water at 23 °C
• カートリッジコード: Code 5 (2-222; O-rings and spear)

詳細

詳細

Device Configuration: カートリッジ

包装

ダブル イージーオープン バッグ

その他情報

これらの製品はFDAの定めたGMP準拠の製造工場で製造されています。

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.

調製ノート

Sterilization Method
135 °C 30 分のSIP 30回; 126 °C 60 分のオートクレーブ滅菌30回

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).

アナリシスノート

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

次の水でフラッシング後USP Oxidizable Substances Testに適合 ≥1 L

TOC/Conductivity
After sterilization and a controlled water flush of 3.5 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.

法的情報

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

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