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KTGRA04TT3

Millipore

Aervent® 0.2 µm, Opticap® XL Capsule

Opticap® XL 4, inlet connection diam. 1.5 in., pore size 0.2 μm, cartridge nominal length 7.7 in. (19.6 cm)

Synonym(s):

Opticap XL capsule with Aervent filter, 0.2 µm

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About This Item

UNSPSC Code:
23151806
eCl@ss:
32031690

material

PTFE
polypropylene
polypropylene housing
polypropylene support
polypropylene vent cap
silicone seal

Quality Level

400

sterility

non-sterile

sterilization compatibility

autoclavable compatible

product line

Opticap® XL 4

feature

hydrophobic

manufacturer/tradename

Opticap®

parameter

≤9 mL/min nitrogen diffusion at 965 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
2.8 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 23 °C
80 psig max. inlet pressure

technique(s)

gas filtration: suitable

L

19.6 cm (7.7 in.)

W

3.3 in.

cartridge nominal length

7.7 in. (19.6 cm)

diam.

8.4 cm (3.3 in.)

filtration area

0.21 m2

inlet connection diam.

1.5 in.

inlet to outlet W

19.6 cm (7.7 in.)

outlet connection diam.

1.5 in.

impurities

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

gravimetric extractables

≤15 mg

matrix

Aervent®

pore size

0.2 μm pore size

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
 outlet sanitary flange
 (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

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General description

Device Configuration: Capsule

Packaging

Double Easy-Open bag

Linkage

Replaces: KTGR04TC3

Preparation Note

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).

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: ≤0.25 mL/min @ 2.6 bar (38 psig)

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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