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KR03A10FF1

Millipore

Opticap® XL10 Polygard®-CR 3.0 µm 3/4 in. TC/TC

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About This Item

UNSPSC代码:
23151806

质量水平

物料

polypropylene
polypropylene housing (PP)
polypropylene support
polypropylene vent cap
silicone seal

无菌性

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

灭菌适用性

autoclavable compatible

参数

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

长度

33.5 cm (13.2 in.)

纯化柱标称长度

10 in. (25 cm)

设备尺寸

10 in.

直径

10.7 cm (4.2 in.)
4.2 in. (10.7 cm)

入口接头直径

3/4 in.

outlet W

33.5 cm (13.2 in.)

出口接头直径

3/4 in.

杂质

≤0.5 EU/mL Aqueous extraction (LAL test)

基质

Polygard®-CR

孔径

3.0 μm nominal pore size
3.0 μm

配件

inlet sanitary flange
outlet sanitary flange
19 mm (3/4 in.) sanitary flange drain/vent

适用性

suitable for endotoxin

一般描述

A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.

包装

Double Easy-Open bag

分析说明

The extractables level was equal to or less than 55 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

其他说明

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.

法律信息

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

免责声明

All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

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