KVGBA05HH1

Opticap 除菌级 XL5 Durapore 疏水性 0.22 µm 9/16 in.HB/HB

inlet connection diam. 9/16 in., Opticap^® XL 5, pore size 0.22 μm, cartridge nominal length 5 in. (12.5 cm)

• 别名: 疏水性Durapore^® 0.22 µm，Opticap^® XL囊式
• 分類程式碼代碼: 23151806

属性

• 材料: PVDF ; polypropylene ; polypropylene housing; polypropylene support; polypropylene vent cap; silicone seal
• 品質等級: 400
• 法律遵循: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• 無菌: non-sterile
• 滅菌相容性: autoclavable compatible
• 產品線: Opticap^® XL 5
• 特點: hydrophobic
• 製造商／商標名: Opticap^®
• 參數: ≤5 mL/min nitrogen diffusion at 1.7 bar (25 psig) and 23 °C (in 60/40% IPA/water); 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward); 1.0 bar max. inlet pressure (15 psi) at 80 °C; 2.8 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 3.4 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 23 °C; 80 psig max. inlet pressure
• 技術: sterile filtration: suitable
• 長度: 8.4 in.
• 寬度: 5.7 in.
• 柱標稱長度: 5 in. (12.5 cm)
• 直徑: 14.5 cm (5.7 in.)
• 過濾面積: 0.35 m²
• 入口接頭直徑: 9/16 in.
• 入口到出口寬度: 21.3 cm (8.4 in.)
• 出口接頭直徑: 9/16 in.
• 雜質: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• 基質: Durapore^®
• 孔徑: 0.22 μm pore size
• 起泡點: ≥1170 mbar (17 psig), nitrogen with 60/40% IPA/water at 23 °C
• 接頭: 1/4 in. drain/vent hose barb (with double O-ring Seal); (14 mm (9/16 in.) Hose Barb Inlet and Outlet)

说明

一般說明

Device Configuration: 取样皿滤膜

包裝

Double Easy-Open bag

其他說明

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

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 installation section of OPTICAP^® XL Capsules and OPTICAP^® XLT Capsules user guide
• Storage Statement: Store in dry location
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

準備報告

Sterilization Method
20 autoclave cycles of 30 min @ 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 21 CFR 210.3 (b) (6).

分析報告

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

法律資訊

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

免責聲明

EMD Millipore Corporation certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark.