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KTGRA05FF1

Millipore

Opticap® XL5 Aervent® KTGR

inlet connection diam. 3/4 in., pore size 0.2 μm, cartridge nominal length 5 in. (13 cm)

Synonym(s):
Aervent KTGR Opticap XL5 Capsule
eCl@ss:
32031690

Quality Level

material

PTFE
polypropylene
polypropylene housing
polypropylene support
polypropylene vent cap
silicone seal

feature

hydrophobic

manufacturer/tradename

Aervent®

parameter

≤12 mL/min air diffusion at 965 mbar (14 psig) and 23 °C (in 70/30%IPA/water)
≤12 mL/min nitrogen diffusion at 970 mbar (14 psig) and 23 °C (in 70/30% IPA/water)
1.0 bar max. differential pressure (15 psid) at 80 °C (Forward)
1.0 bar max. inlet pressure (15 psi) at 80 °C (Forward)
2.8 bar max. inlet pressure (40 psi) at 60 °C (Forward)
25 °C max. inlet temp.
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)
80 psig max. inlet pressure

L

21.0 cm (8.3 in.)

cartridge nominal length

5 in. (13 cm)

diam.

10.7 cm (4.2 in.)

filtration area

0.32 m2

inlet connection diam.

3/4 in.

inlet to outlet W

21.0 cm (8.3 in.)

outlet connection diam.

3/4 in.

overall size

5 in.

impurities

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

gravimetric extractables

≤14 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

fitting

1/4 in. drain/vent hose barb (with double O-ring Seal)
inlet sanitary flange
19 mm (3/4 in.) inlet/outlet sanitary flange
outlet sanitary flange

Related Categories

General description

Device Configuration: Capsule

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

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

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: ≤0.38 mL/min @ 2.6 bar (38 psig) per sample

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
OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

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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