跳转至内容
Merck
CN

KGW6A02HH3

Polysep™ II 1.0/0.5 µm nominal, Opticap® XL Capsule

inlet connection diam. 9/16 in., Opticap® XL 2, pore size 1.0/0.5 μm, cartridge nominal length 2 in. (5 cm)

别名:

Opticap XL2 Polysep II 1.0/0.5 μm 9/16 in. HB/HB

登录 查看组织和合同定价。

选择尺寸

关于此项目

eCl@ss:
32031610
UNSPSC Code:
23151806

主要文件

查看所有文档
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

Polysep™ II 1.0/0.5 µm nominal, Opticap® XL Capsule, inlet connection diam. 9/16 in., Opticap® XL 2, pore size 1.0/0.5 μm, cartridge nominal length 2 in. (5 cm)

material

borosilicate glass fiber (BGF) prefilter
mixed cellulose esters (MCE)
polypropylene
polypropylene housing
polypropylene support
polypropylene vent cap
silicone seal

reg. compliance

meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)

sterility

non-sterile

sterilization compatibility

autoclavable compatible

product line

Opticap® XL 2

feature

hydrophilic

manufacturer/tradename

Opticap®

parameter

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.
3.5 bar max. differential pressure (50 psid) at 25 °C
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure

technique(s)

prefiltration: suitable

L

14.2 cm (5.6 in.)

W

3.3 in.

cartridge nominal length

2 in. (5 cm)

diam.

14.5 cm (5.7 in.)

filtration area

0.06 m2

inlet connection diam.

9/16 in.

inlet to outlet W

14.2 cm (5.6 in.)

outlet connection diam.

9/16 in.

impurities

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

gravimetric extractables

≤45 mg/capsule

matrix

Polysep™ II

pore size

1.0/0.5 μm nominal pore size
1.0/0.5 μm pore size

input

sample type liquid

fitting

inlet hose barb
 outlet hose barb
 (14 mm (9/16 in.) Hose Barb Inlet and Outlet)

Quality Level

400

正在寻找类似产品? 访问 产品对比指南

Analysis Note

Gravimetric Extractables: after a 600 mL flush and 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L

Disclaimer

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.

Features and Benefits

Format: Double Layer

General description

Device Configuration: Capsule

Other Notes

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 to the first page of Visual Inspection Guide and introduction section of the Mixed cellulose esters Tech Brief
  • Storage Statement: Please refer to the Mixed cellulose esters Tech Brief
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.
Replaces: SN1M017A01
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
3 autoclave cycles of 30 min @ 121 °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).

Legal Information

OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany
Polysep is a trademark of Sigma-Aldrich Co. LLC

存储类别

11 - Combustible Solids

wgk

WGK 2

法规信息

新产品
此项目有

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.

联系客户支持