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KGW3A3THH1

Millipore

Polysep II 1.0/0.2 µm nominal, Opticap® XLT Capsule

inlet connection diam. 5/8 in., Opticap® XLT 30, pore size 1.0/0.2 μm, cartridge nominal length 30 in. (75 cm)

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Synonym(s):
Opticap XLT30 Polysep II 1.0/0.2 μm 5/8 in. HB
eCl@ss:
32031610

material

borosilicate glass fiber (BGF) membrane
mixed cellulose esters (MCE) membrane
polypropylene
polypropylene housing
polypropylene support
polypropylene vent cap
silicone seal

Quality Level

reg. compliance

meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)

sterility

non-sterile

sterilization compatibility

autoclavable compatible

product line

Opticap® XLT 30

feature

hydrophilic

manufacturer/tradename

Opticap®

parameter

1.0 bar max. inlet pressure (15 psi) at 80 °C
2.75 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
3.5 bar max. differential pressure (50 psid) at 25 °C
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure

technique(s)

prefiltration: suitable

L

87.1 cm (34.3 in.)

cartridge nominal length

30 in. (75 cm)

filtration area

1.38 m2

inlet connection diam.

5/8 in.

inlet to outlet W

19.8 cm (7.8 in.)

outlet connection diam.

5/8 in.

impurities

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

gravimetric extractables

≤435 mg/capsule

matrix

Polysep II

pore size

1.0/0.2 μm nominal pore size
1.0/0.2 μm pore size

input

sample type liquid

fitting

inlet hose barb
outlet hose barb
(16 mm (5?8 in.) Hose Barb Inlet and Outlet)

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KGW6A3THH1KGW2A3THH1KGW9A3THH1
matrix

Polysep II

matrix

Polysep II

matrix

Polysep II

matrix

Polysep II

pore size

1.0/0.2 μm nominal pore size, 1.0/0.2 μm pore size

pore size

1.0/0.5 μm nominal pore size, 1.0/0.5 μm pore size

pore size

1.0/1.2 μm nominal pore size, 1.2/1.0 μm pore size

pore size

2.0/1.2 μm nominal pore size, 2.0/1.2 μm pore size

feature

hydrophilic

feature

hydrophilic

feature

hydrophilic

feature

hydrophilic

sterility

non-sterile

sterility

non-sterile

sterility

non-sterile

sterility

non-sterile

technique(s)

prefiltration: suitable

technique(s)

prefiltration: suitable

technique(s)

prefiltration: suitable

technique(s)

prefiltration: suitable

General description

Device Configuration: Capsule
T-line/Gauge Port: T-line

Features and Benefits

Format: Double Layer

Packaging

Double Easy-Open bag

Other Notes

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
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 to the first page of Visual Inspection Guide and introduction section of the Mixed cellulose esters Tech Brief
  • Storage Statement: Please refer to the Mixed cellulose esters Tech Brief
  • Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Preparation Note

Sterilization Method
3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable
This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

Analysis Note

Gravimetric Extractables: after a 15 L flush and 24 hours in water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥15 L

Legal Information

OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany
Polysep is a trademark of Sigma-Aldrich Co. LLC

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2


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