K030A51HH1

Opticap XL1 Clarigard 3.0 µm 9/16 in.HB/HB

inlet connection diam. 9/16 in., pore size 3.0 μm, cartridge nominal length 1 in. (2.5 cm)

• 别名: Opticap^® XL1 Clarigard过滤器^®
• 分類程式碼代碼: 23151806
• eCl@ss: 32031690

属性

• 材料: 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)
• 製造商／商標名: Opticap^®
• 參數: 1.0 bar max. inlet pressure (15 psi) at 80 °C; 2.75 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 4.8 bar max. differential pressure (70 psid) at 20 °C; 5.5 bar max. inlet pressure (80 psi) at 23 °C; 80 psig max. inlet pressure
• 長度: 21.6 cm (8.5 in.)
• 柱標稱長度: 1 in. (2.5 cm)
• 直徑: 10.7 cm (4.2 in.)
• 入口接頭直徑: 9/16 in.
• 入口到出口寬度: 21.6 cm (8.5 in.)
• 出口接頭直徑: 9/16 in.
• 雜質: ≤0.25 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• 重量法萃取物: ≤10 mg/capsule
• 基質: Clarigard^®
• 孔徑: 3.0 μm nominal pore size; 3.0 μm pore size
• 輸入: sample type liquid
• 接頭: inlet hose barb; 14 mm (9/16 in.) inlet/outlet hose barb; outlet hose barb

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
3 autoclave cycles of 30 min @ 126 °C; not in-line steam sterilizable

This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

分析報告

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

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L

法律資訊

CLARIGARD 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.