跳转至内容
Merck
CN

MFGB02GH3

Millipak® Final Fill 20 Durapore®

Inlet: 1/4 in. Hose Barb Outlet: 1/4 in. Hose Barb Vent: 1/8 in. Hose Barb

别名:

Hydrophobic Durapore® 0.22 µm, Millipak® Final Fill Capsule

登录 查看组织和合同定价。

选择尺寸

关于此项目

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

Millipak® Final Fill 20 Durapore®, Millipak® Final Fill 20

material

polysulfone device, polysulfone support

agency

meets EP 2.6.14, meets JP 4.01, meets USP 85

sterility

irradiated, non-sterile

sterilization compatibility

gamma compatible

product line

Millipak® Final Fill 20

feature

hydrophilic

manufacturer/tradename

Millipak®

parameter

0.35 bar max. differential pressure (5 psid) at 121 °C (Reverse), 0.51 L/min flow rate at 0.69 bar (ΔP), 10 psi max. differential pressure (0.7 bar) at 25 °C (Reverse), 20 L process volume, 25 psi max. differential pressure (1.7 bar) at 80 °C (Forward), 3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse; intermittent), 5.5 bar max. inlet pressure (80 psi) at 25 °C, 50 psi max. differential pressure (3.5 bar) at 25 °C (Forward), 60 psi max. differential pressure (4.1 bar) at 25 °C (Forward)

technique(s)

sterile filtration: suitable

L

3.2 in.

W

3.0 in.

filter filtration area

100 cm2

impurities

<0.25 EU/mL USP bacterial endotoxins (LAL test, per device; aqueous extraction), <0.25 EU/mL bacterial endotoxins (LAL test, per device; aqueous extraction)

matrix

Durapore®

pore size

0.22 μm pore size

fitting

(6 mm (1/4 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

相关类别

General description

Device Configuration: Capsule

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method: Device integrity and retention was maintained after 3 autoclave cycles of 90 minutes at 126  °C. Devices can withstand a dose ≤40  kGy gamma exposure.

This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b)(6), validated based on large volume parenteral specifications as detailed in USP 788 Particulate Matter in Injections

Analysis Note

Bacterial Grow-Through: Quantitative retention of 1 x 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per ASTM® F838 methodology.

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 general guidelines section of user guide shipped with this product
  • Storage Statement: Please refer user guide shipped with this product
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations

These products are manufactured in a facility which is certified to ISO 9001:2015 Quality Management Systems.

Legal Information

ASTM is a registered trademark of American Society for Testing and Materials
ATCC is a registered trademark of American Type Culture Collection
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPAK is a registered trademark of Merck KGaA, Darmstadt, Germany

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