Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

CTGR02TP1

Millipore

Aervent® 0.2 µm, Cartridge

pore size 0.2 μm, cartridge nominal length 20 in. (51 cm), Code 0 (2-222; O-rings)

Synonym(s):

Aervent CTGR Cartridge Filter 20 in. 0.2 µm Code 0

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
23151806
eCl@ss:
32031690

material

PTFE
polypropylene
polypropylene support
silicone seal

Quality Level

sterility

non-sterile

sterilization compatibility

steam-in-place compatible

product line

Aervent®

feature

hydrophobic

manufacturer/tradename

Aervent®

parameter

≤48 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)

technique(s)

gas filtration: suitable

L

20 in.

W

2.7 in.

cartridge nominal length

20 in. (51 cm)

diam.

6.9 cm (2.7 in.)

filtration area

1.3 m2

impurities

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

gravimetric extractables

≤70 mg/cartridge

matrix

Aervent®

pore size

0.2 μm pore size

input

sample type gas

bubble point

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

cartridge code

Code 0 (2-222; O-rings)

General description

Device Configuration: Cartridge

Features and Benefits

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.

Packaging

Double Easy-Open bag

Quality

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

Preparation Note

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).

Analysis Note

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
HydroCorr: ≤1.5 mL/min @ 2.6 bar (38 psig) per 20 in cartridge

Other Notes

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.

Legal Information

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

Not finding the right product?  

Try our Product Selector Tool.


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service