KGEPG3TTT1

Millipore Express^® SHF 0.2µm, Opticap^® XLT 30 Capsule

Fittings 1-1/2 in. TC, Gamma Compatible

• Synonim(y): Opticap XLT 30 Millipore Express SHF Gamma Compatible 0.2 μm 1-1/2 in. TC, Millipore Express^® SHF, Opticap^® XLT Capsule
• UNSPSC Code: 23151806

Właściwości

• Nazwa produktu: OPTICAP^® XLT 30 Capsule Media: MILLIPORE EXPRESS^® SHF 0.2 µm, Chemistry: Hydrophilic Polyethersulfone (PES) Inlet: 1-1/2 in. Sanitary Flange Outlet: 1-1/2 in. Sanitary Flange T-line Max Operating Pressure: 80 psi @ 25 °C
• Quality Segment: 400
• material: polyester support, polyethersulfone membrane, polypropylene housing, polypropylene vent cap, silicone O-ring (gamma-stable), 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; gamma compatible; x-ray compatible
• product line: Opticap^® XLT
• feature: hydrophilic
• manufacturer/tradename: Millipore Express^®
• parameter: 1 bar max. differential pressure (15 psi) at 80 °C, 1 bar max. inlet pressure (15 psi) at 80 °C, 2.8 bar max. inlet pressure (40 psi) at 60 °C, 5.5 bar max. differential pressure (80 psi) at 25 °C, 5.5 bar max. inlet pressure (80 psi) at 25 °C, 6.9 bar max. differential pressure (100 psi) at 25 °C (Forward; Intermittent), 6.9 bar max. inlet pressure (100 psi) at 25 °C (Intermittent)
• technique(s): sterile filtration: suitable
• L: 87.1 cm (34.3 in.)
• W: 7.8 in.
• cartridge nominal length: 30 in. (75 cm)
• diam.: 10.7 cm (4.2 in.)
• filtration area: 1.71 m² (18.4 ft²)
• 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 USP bacterial endotoxins (LAL test, sample aqueous extraction)
• matrix: Millipore Express^® SHF
• pore size: 0.2 μm
• bubble point: ≥4000 mbar (58 psig), air with water at 23 °C
• fitting: 38 mm (1 1/2 in.) inlet sanitary flange, 38 mm (1 1/2 in.) outlet sanitary flange

Opis

General description

Device Configuration: Capsule

T-line/Gauge Port: T-line

Packaging

Double Easy-Open bag

Preparation Note

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).

Sterilization Method
Gamma compatible to 45 kGy; 3 autoclave cycles of 60 min @ 123 °C; not in-line steam sterilizable

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 33 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 ≥4.5 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

ASTM is a registered trademark of American Society for Testing and Materials

MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany

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