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KPGES003FF3

Millipore

Millipore Express® PHF 0.2µm, Opticap® XL 300 Capsule

Fittings 3/4 in. TC/TC, Sterile

别名:

Opticap XL 300 Millipore Express PHF Sterile 0.2 μm 3/4 in. TC/TC

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关于此项目

UNSPSC代码:
23151806
价格与库存信息目前不能提供
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产品名称

Millipore Express® PHF, Opticap® XL 囊式, Opticap® XL 3, sterile, inlet connection diam. 3/4 in., cartridge nominal length 4.7 in. (11.9 cm)

物料

polyethersulfone
polyethylene support
polypropylene (gamma-stable)
polypropylene housing
polypropylene vent cap
polysulfone
silicone seal

质量水平

400

管理合规性

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

无菌性

irradiated
sterile

产品线

Opticap® XL 3

特点

hydrophilic

制造商/商品名称

Millipore Express®

参数

≤2.8 mL/min air diffusion at 2.8 bar (40 psig) and 23 °C (in water)
1.0 bar max. inlet pressure (15 psi) at 80 °C
1000 bar max. differential pressure (15 psi) at 80 °C
2.75 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
5.5 bar max. inlet pressure (80 psi) at 25 °C
5500 mbar max. differential pressure (80 psi) at 25 °C
80 psig max. inlet pressure

技术

bioburden reduction: suitable

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KVEPG2TTH1

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pore size

0.1 μm pore size

pore size

0.1 μm pore size

pore size

0.1 μm pore size

pore size

0.1 μm pore size

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

product line

Opticap® XLT 10

product line

Opticap® XLT 20

product line

Opticap® XLT 30

product line

Opticap® XLT 20

matrix

Millipore Express® SHR

matrix

Millipore Express® SHR

matrix

Millipore Express® SHR

matrix

Millipore Express® SHR

material

polyester support, polypropylene housing, silicone seal, polypropylene device, polypropylene vent cap

material

polyester support, polypropylene device, polypropylene housing, polypropylene vent cap, silicone seal

material

polyester support, polypropylene device, polypropylene housing, polypropylene vent cap, silicone seal

material

polyester support, polypropylene device, polypropylene housing, polypropylene vent cap, silicone seal

manufacturer/tradename

Millipore Express®

manufacturer/tradename

Millipore Express®

manufacturer/tradename

Millipore Express®

manufacturer/tradename

Millipore Express®

一般描述

Device Configuration: 取样皿滤膜
Sterile capsules meet current USP and AAMI guidelines for sterility utilizing a validated sterilization cycle.

包装

Double Easy-Open bag

制备说明

Sterilization Method
3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
This product was manufactured with a Millipore Express® 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 of membrane used in this filter were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
TOC/Conductivity
After sterilization and a controlled water flush of 2.5 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L

其他说明

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 wetting instructions of Filters with MILLIPORE EXPRESS® Membrane user guide
  • Storage Statement: Please refer Filters with MILLIPORE EXPRESS® Membrane user guide
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

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

法律信息

ASTM is a registered trademark of American Society for Testing and Materials
MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany
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.

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