MSP000812

Durapore^® 0.22 µm、カートリッジ

cartridge nominal length 10 in. (25 cm), Code 7 (2-226; O-rings w/locking-tabs)

• 別名: Durapore Cartridge Filter 10 in. 0.22 μm Code 7
• UNSPSCコード: 23151806
• eCl@ss: 27293007

特性

• 物質: PVDF
• 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^®; EMPROVE^® Filter
• 特徴: hydrophilic
• メーカー／製品名: Durapore^®
• 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)
• ろ過面積: 0.69 m²
• 不純物: <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• 重量分析抽出物: ≤20 mg/cartridge
• Matrix: Durapore^®
• ポアサイズ: 0.22 μm
• 入力: sample type liquid
• カートリッジコード: Code 7 (2-226; O-rings w/locking-tabs)

詳細

詳細

Device Configuration: カートリッジ

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

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.

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

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