KV03A10FF1

Multimedia Durapore^® 0.2/0.22 µm, Opticap^® XL Capsule

Opticap^® XL 10, cartridge nominal length 10 in. (25 cm), filter diam. 4.2 in. (10.7 cm)

• UNSPSCコード: 23151806

特性

• 物質: mixed cellulose esters (MCE) prefilter; polypropylene filter; polypropylene housing; polypropylene support; silicone seal
• 品質水準: 400
• 法規制遵守: FDA 21CFR177-182 (all component materials)
• 無菌性: non-sterile
• 滅菌適合性: autoclavable compatible
• 製品種目: Opticap^® XL 10
• 特徴: hydrophilic
• メーカー／製品名: Opticap^®
• パラメーター: ≤13.3 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water); 1 bar max. inlet pressure (15 psi) at 80 °C; 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward:); 2.75 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 3.5 bar max. differential pressure (50 psid) 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; 80 psig max. inlet pressure
• テクニック: prefiltration: suitable
• カートリッジの長さ（公称）: 10 in. (25 cm)
• device L: 33.5 cm (13.2 in.)
• device size: 10 in.
• フィルタ直径: 4.2 in. (10.7 cm)
• filter filtration area: 0.2 m²
• 入口接続部直径: 3/4 in.
• 出口接続部直径: 3/4 in.
• 不純物: ≤0.5 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.5 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)
• マトリックス: Multimedia Durapore^®
• pore size: 0.2/0.22 μm pore size
• 泡立ち点: ≥3450 mbar (50 psig), air with water at 23 °C
• フィッティング: 1/4 in. fitting (vent/drain hose barb with double O-ring seal); (19 mm (3/4 in.) Sanitary Flange Inlet and Outlet)

詳細

詳細

Device Configuration: Capsule

包装

Double Easy-Open bag

調製ノート

Sterilization Method:
3 autoclave cycles of 60min at 126°C; not in-line steam sterilizable

This product was manufactured with a Durapore^® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21CFR210.3(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.

Gravimetric Extractables: ≤ 50 mg per capsule after 24 hours in water at controlled room temperature.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 5 L

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 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

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

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