Merck
CN
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KTGRA04TH3

Millipore

Aervent® 0.2 µm，Opticap® XL囊式

Opticap® XL 4, inlet connection diam. 1.5 in., pore size 0.2 μm, cartridge nominal length 4 in. (10 cm)

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别名:
Opticap XL 4 with Aervent - 4" 0.2um TC/HB 3pk
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 4

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

7.7 in.

宽度

3.3 in.

纯化柱标称长度

4 in. (10 cm)

直径

8.4 cm (3.3 in.)

过滤面积

0.21 m2

入口接头直径

1.5 in.

出口接头直径

9/16 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)
 inlet sanitary flange
 outlet hose barb
 (38 mm (1 1/2 in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet)

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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
3 autoclave cycles of 60 min @ 123 °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.

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