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Merck
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CTGR01TP1

Millipore

Aervent® 0.2 µm小柱

pore size 0.2 μm, cartridge nominal length 10 in. (25 cm), Code 0

别名:

Aervent CTGR Cartridge Filter 10 in. 0.2 µm Code 0

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About This Item

分類程式碼代碼:
23151806
eCl@ss:
32031690

材料

PTFE
polypropylene
polypropylene support
silicone seal

品質等級

無菌

non-sterile

滅菌相容性

steam-in-place compatible

產品線

Aervent®

特點

hydrophobic

製造商/商標名

Aervent®

參數

≤24 mL/min nitrogen diffusion at 970 mbar (14 psig) and 23 °C (in 70/30% IPA/water)
1.7 bar max. inlet pressure (25 psi) at 80 °C
1.8 bar max. differential pressure (25 psid) at 80 °C (Forward)
4.1 bar max. differential pressure (60 psid) (Reverse; intermittent)
4.1 bar max. inlet pressure (60 psi) (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 (Forward)

技術

gas filtration: suitable

長度

10 in.

寬度

2.7 in.

柱標稱長度

10 in. (25 cm)

直徑

6.9 cm (2.7 in.)

過濾面積

0.65 m2

雜質

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

重量法萃取物

≤35 mg/cartridge

基質

Aervent®

孔徑

0.2 μm pore size

輸入

sample type gas

起泡點

≥1100 mbar (16 psig), nitrogen with 70/30% IPA/water at 23 °C

柱代碼

Code 0

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一般說明

Device Configuration: Cartridge

特點和優勢

Rated for aerosol retention of a total challenge of 108–1010 plaque forming units of ΦX-174 virus particles at 85 Nm3/h (50 SCFM) per cartridge.

包裝

Double Easy-Open bag

品質

Retains Brevundimonas diminuta liquid aerosol for 21 days at a minimum challenge of 10⁷ CFU/cm²

準備報告

Sterilization Method
150 (100 forward/50 reverse) SIP cycles of 30 min @ 145 °C
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.
HydroCorr: ≤0.75 mL/min @ 2.6 bar (38 psig) per 10 in cartridge
Gravimetric Extractables: after 24 hours in a 70/30% IPA/water mixture at controlled room temperature

其他說明

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 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.

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

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