MilliporeSigma
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KPHLS1TTH1

Millipore

Durapore® 0.45 µm, Opticap® XLT Capsule

Opticap® XLT 10, cartridge nominal length 14.8 in. (37.6 cm), filter diam. 4.2 in. (10.7 cm)

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material

polyester support
polyethylene support
polypropylene filter
polypropylene housing
silicone seal

Quality Level

reg. compliance

FDA 21CFR177-182 (all component materials)

sterility

sterile; irradiated

product line

Opticap® XLT 10

feature

hydrophilic

manufacturer/tradename

Opticap®

parameter

≤15.0 mL/min air diffusion at 3.9 bar (56 psig) and 23 °C (in water)
1 bar max. inlet pressure (15 psi) at 80 °C
2.1 bar max. differential pressure (30 psid) at 4-40 °C (Reverse:)
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 (Forward:)
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure

technique(s)

bioburden reduction: suitable

cartridge nominal length

14.8 in. (37.6 cm)

device L

37.6 cm (14.8 in.)

device size

10 in.

filter diam.

4.2 in. (10.7 cm)

filter filtration area

0.62 m2

inlet connection diam.

1-1/2 in.

inlet to outlet width

37.6 cm (14.8 in.)

outlet connection diam.

5/8 in.

impurities

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

matrix

Durapore®

pore size

0.45 μm pore size

bubble point

≥1930 mbar (28 psig), air with water at 23 °C

fitting

1/4 in. fitting (vent/drain hose barb with double O-ring seal)
(38 mm (1 1/2 in.) Sanitary Flange Inlet and 16 mm (5?8 in.) Hose Barb Outlet)

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KPHLS2TTH1KPHLS3TTT1KPHLS1TTT1
sterility

sterile; irradiated

sterility

sterile; irradiated

sterility

sterile; irradiated

sterility

sterile; irradiated

product line

Opticap® XLT 10

product line

Opticap® XLT 20

product line

Opticap® XLT 30

product line

Opticap® XLT 10

feature

hydrophilic

feature

hydrophilic

feature

hydrophilic

feature

hydrophilic

technique(s)

bioburden reduction: suitable

technique(s)

bioburden reduction: suitable

technique(s)

bioburden reduction: suitable

technique(s)

bioburden reduction: suitable

matrix

Durapore®

matrix

Durapore®

matrix

Durapore®

matrix

Durapore®

General description

Device Configuration: Capsule

Preparation Note

Sterilization Method:
Minimum sterilization up to 25 kGy. 3 autoclave cycles of 60min at 3°C; not in-line steam sterilizable

Analysis Note

Gravimetric Extractables: ≤ 25 mg per capsule after 24 hours in water at controlled room temperature.
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 1500 mL

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 installation section of Opticap® XL Capsules and Opticap® XLT Capsules user guide
  • Storage Statement: Store in dry location
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations

Legal Information

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

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