Merck
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安全信息

KGW3A1TTT1

Millipore

Polysep™ II 1.0/0.2 µm nominal, Opticap® XLT Capsule

Opticap® XLT 10, inlet connection diam. 1.5 in., pore size 1.0/0.2 μm, cartridge nominal length 10 in. (25 cm)

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别名:
Opticap XLT10 Polysep II 1.0/0.2 μm 1-1/2 in. TC
eCl@ss:
32031610

物料

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

质量水平

400

reg. compliance

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

无菌性

non-sterile

sterilization compatibility

autoclavable compatible

产品线

Opticap® XLT 10

特点

hydrophilic

manufacturer/tradename

Opticap®

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.
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

长度

37.6 cm (14.8 in.)

宽度

6.0 in.

cartridge nominal length

10 in. (25 cm)

过滤面积

0.46 m2

inlet connection diam.

1.5 in.

inlet to outlet W

15.2 cm (6.0 in.)

outlet connection diam.

1.5 in.

杂质

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

gravimetric extractables

≤145 mg/capsule

基质

Polysep™ II

pore size

1.0/0.2 μm nominal pore size
1.0/0.2 μm pore size

input

sample type liquid

配件

inlet sanitary flange
 outlet sanitary flange
 (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

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相关类别

一般描述

Device Configuration: 取样皿滤膜
T-line/Gauge Port: T-line

特点和优势

Format: Double Layer

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 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.

制备说明

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).

分析说明

Gravimetric Extractables: after a 5 L flush and 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥5 L

法律信息

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

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.

储存分类代码

11 - Combustible Solids

WGK

WGK 2

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