5A10FF1

Opticap^® XL10 Polygard^® CR

inlet connection diam. 3/4 in., pore size 25.0 μm, cartridge nominal length 10 in. (25 cm)

• 同義詞: Opticap^® XL10 Polygard^®-CR 25 µm 3/4 in. TC/TC
• 分類程式碼代碼: 23151806
• eCl@ss: 32031690

屬性

• 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 25 °C; 80 psig max. inlet pressure
• 長度: 33.5 cm (13.2 in.)
• 柱標稱長度: 10 in. (25 cm)
• 直徑: 10.7 cm (4.2 in.)
• 入口接頭直徑: 3/4 in.
• 入口到出口寬度: 33.5 cm (13.2 in.)
• 出口接頭直徑: 3/4 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)
• 重量法萃取物: ≤55 mg/capsule
• 基質: Polygard^®-CR
• 孔徑: 25.0 μm nominal pore size; 25.0 μm pore size
• 輸入: sample type liquid
• 接頭: inlet sanitary flange; 19 mm (3/4 in.) inlet/outlet sanitary flange; outlet sanitary flange

描述

一般說明

Device Configuration: 取样皿滤膜

特點和優勢

Format: Single Layer

包裝

Double Easy-Open bag

其他說明

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

準備報告

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

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 ≥5 L

法律資訊

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

POLYGARD 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.