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Merck

KHGES2TTT1

Millipore Express® SHC 0.5/0.2µm, Opticap® XLT 20 Capsule

Fittings 1-1/2 in. TC, Sterile

Synonim(y):

Opticap Sterile XLT 20 Millipore Express SHC 0.5/0.2 μm 1-1/2 in. TC

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1 EA

5780,00 zł

5780,00 zł


Przewidywany termin wysyłki06 lutego 2026Szczegóły



Informacje o tej pozycji

UNSPSC Code:
23151806

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Nazwa produktu

Millipore Express® SHC, Opticap® XLT Capsule, Opticap® XLT 20, sterile, inlet connection diam. 1.5 in., pore size 0.5/0.2 μm, cartridge nominal length 20 in. (50 cm)

material

polyester support
polyethersulfone
polypropylene
polypropylene housing
polypropylene vent cap
polysulfone
silicone seal

reg. compliance

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

sterility

irradiated
sterile

product line

Opticap® XLT 20

feature

hydrophilic

manufacturer/tradename

Millipore Express®

parameter

≤62.5 mL/min air diffusion at 2.8 bar (40 psig) and 23 °C (in water)
1.0 bar max. differential pressure (15 psid) at 80 °C (Forward)
1.0 bar max. inlet pressure (15 psi) at 80 °C
100 psi max. differential pressure (6.9 bar) (intermittent)
2.1 bar max. differential pressure (30 psid) at 25 °C (Reverse; intermittent)
2.75 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
5.5 bar max. differential pressure (80 psid) at 25 °C (Forward)
5.5 bar max. inlet pressure (80 psi) at 25 °C
6.9 bar max. differential pressure (100 psid) at 25 °C (Forward; intermittent)
6.9 bar max. inlet pressure (100 psi) at 25 °C (intermittent)
80 psi max. differential pressure (5.5 bar) (continuous)
80 psig max. inlet pressure

technique(s)

sterile filtration: suitable

L

62.5 cm (24.6 in.)

cartridge nominal length

20 in. (50 cm)

diam.

10.7 cm (4.2 in.)

inlet connection diam.

1.5 in.

inlet to outlet W

15.2 cm (6.0 in.)

outlet connection diam.

1.5 in.

impurities

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

matrix

Millipore Express® SHC

pore size

0.5/0.2 μm pore size

bubble point

≥4000 mbar (58 psig), air with 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)

Quality Level

filtration area

1.08 m2

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Ta pozycja
KHGES2THH1KHGEA2TTT1KHGEA2TTH1
pore size

0.5/0.2 μm pore size

pore size

0.5/0.2 μm pore size

pore size

0.5/0.2 μm pore size

pore size

0.5/0.2 μm pore size

filtration area

1.09 m2

filtration area

1.09 m2

filtration area

0.98 m2

filtration area

0.98 m2

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

technique(s)

sterile filtration: suitable

product line

Opticap® XLT 20

product line

Opticap® XLT 20

product line

Opticap® XLT 20

product line

Opticap® XLT 20

material

polyester support, polypropylene , polypropylene vent cap, silicone seal, polyethersulfone , polysulfone , polypropylene housing

material

polyester support, polyethersulfone , polypropylene , polypropylene housing, polypropylene vent cap, polysulfone , silicone seal

material

polyethersulfone , polypropylene , polypropylene housing, polypropylene support, polypropylene vent cap, polysulfone , silicone seal

material

polyethersulfone , polypropylene , polypropylene housing, polypropylene support, polypropylene vent cap, polysulfone , silicone seal

manufacturer/tradename

Millipore Express®

manufacturer/tradename

Millipore Express®

manufacturer/tradename

Millipore Express®

manufacturer/tradename

Millipore Express®

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.
TOC/Conductivity
After sterilization and a controlled water flush of 42 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4 L

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.

General description

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

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.

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable
This product was manufactured with a Millipore Express® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

Legal Information

ASTM is a registered trademark of American Society for Testing and Materials
MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany
OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany
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