跳转至内容
Merck
CN
所有图片(1)

文件

安全信息

KTGRA02NN3

Millipore

Aervent® 0.2 µm，Opticap® XL囊式

Opticap® XL 2, inlet connection diam. 1/4 in., pore size 0.2 μm, cartridge nominal length 2 in. (5 cm)

别名:

Opticap XL 2 with Aervent - 2" 0.2um NPT/NPT 3pk

登录查看公司和协议定价
所有图片(1)

About This Item

UNSPSC代码:
23151806
eCl@ss:
32031690

物料

PTFE
polypropylene
polypropylene housing
polypropylene vent cap
silicone seal

质量水平

400

无菌性

non-sterile

灭菌适用性

autoclavable compatible

产品线

Opticap® XL 2

特点

hydrophobic

制造商/商品名称

Opticap®

参数

1.0 bar max. differential pressure (15 psid) at 80 °C (Forward)
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.
4.1 bar max. differential pressure (60 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 25 °C
80 psig max. inlet pressure

技术

gas filtration: suitable

长度

5.6 in.

宽度

3.3 in.

纯化柱标称长度

2 in. (5 cm)

直径

8.4 cm (3.3 in.)

过滤面积

0.1 m2

入口接头直径

1/4 in.

出口接头直径

1/4 in.

杂质

<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

重量萃取物

≤15 mg

基质

Aervent®

孔径

0.2 μm pore size

配件

1/4 in. drain/vent hose barb (with double O-ring Seal)
 (6 mm (1/4 in.) NPT Inlet and Outlet)

正在寻找类似产品? 访问 产品对比指南

相关类别

一般描述

Device Configuration: 取样皿滤膜

包装

Double Easy-Open bag

其他说明

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 Steam Sterilization & Integrity Testing Procedures guide and first page of Visual Inspection Guide
  • Storage Statement: Store in dry location
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

制备说明

Sterilization Method
30 autoclave cycles of 30 min @ 135 °C; not in-line steam sterilizable
This product was manufactured with a PTFE membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

分析说明

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 a 70/30% IPA/water mixture at controlled room temperature

法律信息

AERVENT is a registered trademark of Merck KGaA, Darmstadt, Germany
ASTM is a registered trademark of American Society for Testing and Materials
OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

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.

Not finding the right product?  

Try our 产品选型工具.

法规信息

新产品

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ （Lot或Batch）字后找到。

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门