CTGR03TP1
Aervent® 0.2 µm, Cartridge
pore size 0.2 μm, cartridge nominal length 30 in. (76 cm), Code 0 (2-222; O-rings)
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
≤72 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
30 in.
W
2.7 in.
cartridge nominal length
30 in. (76 cm)
diam.
6.9 cm (2.7 in.)
filtration area
1.95 m2
impurities
<0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction)
gravimetric extractables
≤105 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)
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General description
Features and Benefits
Packaging
Quality
Preparation Note
150 (100 forward/50 reverse) SIP cycles of 30 min @ 145 °C
Analysis Note
Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
Other Notes
- 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
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