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KWSCA3THH1

Opticap® XLT 30 Capsule Media: Milligard® 1.2 / 0.5 µm Nominal

Chemistry: Mixed Cellulose Esters (MCE) Inlet: 5/8 in. Hose Barb Outlet: 5/8 in. Hose Barb T-line Max Operating Pressure: 80 psi @ 25 °C

동의어(들):

Opticap XLT30 Milligard 1.2/0.5 μm 5/8 in. HB/HB, Milligard® 1.2/0.5 µm nominal, Opticap® XLT Capsule

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제품정보 (DICE 배송 시 비용 별도)

eCl@ss:
32031610
UNSPSC Code:
23151806
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제품 이름

Opticap® XLT 30 Capsule Media: Milligard® 1.2 / 0.5 µm Nominal, Chemistry: Mixed Cellulose Esters (MCE) Inlet: 5/8 in. Hose Barb Outlet: 5/8 in. Hose Barb T-line Max Operating Pressure: 80 psi @ 25 °C

Quality Level

400

material

mixed cellulose esters (MCE) , polyester support, polypropylene , polypropylene housing, polypropylene vent cap, silicone seal

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.)

W

7.8 in.

cartridge nominal length

30 in. (75 cm)

filtration area

2.0 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

≤165 mg/capsule

matrix

Milligard®

pore size

1.2/0.5 μm nominal pore size, 1.2/0.5 μm pore size

input

sample type liquid

fitting

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

General description

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

Features and Benefits

Filter Grade: Standard Milligard® Media
Format: Double Layer

Packaging

Double Easy-Open bag

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

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.

Legal Information

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

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KWSCA3THH104053252604393