CV0601TP3

Multimedia Durapore^® 0.5/0.22 µm、カートリッジ

pore size 0.5/0.22 μm, cartridge nominal length 10 in. (25 cm), Code 0 (2-222; O-rings)

• 別名: Durapore Multimedia Cartridge Filter 10 in. 0.5+0.22 μm Code 0
• UNSPSCコード: 23151806
• eCl@ss: 27293007

特性

• 物質: PVDF ; mixed cellulose esters (MCE) ; mixed cellulose esters (MCE) prefilter; polypropylene ; polypropylene support; silicone seal
• 品質水準: 400
• 法規制遵守: 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: ≤13.3 mL/min air diffusion at 2.75 bar (40 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); 3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse; intermittent); 3.5 bar max. inlet pressure (50 psi) at 25 °C (Reverse; Intermittent); 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)
• 重量分析抽出物: ≤45 mg/cartridge
• Matrix: Multimedia Durapore^®
• pore size: 0.5/0.22 μm pore size
• 入力: sample type liquid
• 泡立ち点: ≥3450 mbar (50 psig), air with water at 23 °C
• カートリッジコード: Code 0 (2-222; O-rings)

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
123 °C 30 分のオートクレーブ滅菌またはSIP 6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 ≥5 L

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

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

安全性情報

• ピクトグラム: GHS02
• シグナルワード: Danger
• 危険有害性情報: H228
• 注意書き: P210 - P240 - P241 - P280 - P370 + P378
• 危険有害性の分類: Flam. Sol. 1
• 保管分類コード: 4.1B - Flammable solid hazardous materials
• WGK: WGK 3