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Merck
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KTGRA04NN3

Millipore

Aervent® 0.2 µm,Opticap® XL囊式

inlet connection diam. 1/4 in., Opticap® XL 4, pore size 0.2 μm, cartridge nominal length 4 in. (10 cm)

别名:

Opticap XL 4 with Aervent - 4" 0.2um NPT/NPT 3pk

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About This Item

分類程式碼代碼:
23151806
eCl@ss:
32031690

材料

PTFE
polypropylene
polypropylene housing
polypropylene vent cap
silicone seal

品質等級

無菌

non-sterile

滅菌相容性

autoclavable compatible

產品線

Opticap® XL 4

特點

hydrophobic

製造商/商標名

Opticap®

參數

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

技術

gas filtration: suitable

長度

7.7 in.

寬度

3.3 in.

柱標稱長度

4 in. (10 cm)

直徑

8.4 cm (3.3 in.)

過濾面積

0.21 m2

入口接頭直徑

1/4 in.

出口接頭直徑

1/4 in.

雜質

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

重量法萃取物

≤15 mg

基質

Aervent®

孔徑

0.2 μm pore size

接頭

1/4 in. drain/vent hose barb (with double O-ring Seal)
(6 mm (1/4 in.) NPT Inlet and Outlet)

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一般說明

Device Configuration: 取样皿滤膜

包裝

Double Easy-Open bag

其他說明

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.

準備報告

Sterilization Method
30 autoclave cycles of 30 min @ 135 °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).

分析報告

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

法律資訊

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

免責聲明

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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