KPGEA1TBB1

Millipore Express^® PHF 0.2µm, Opticap^® XLT 10 Capsule

Fittings 1 in. HB/HB, Autoclavable

• Synonym(s): Opticap XLT 10 Millipore Express PHF Autoclavable 0.2 m 1 in. HB/HB, Millipore Express^® PHF, Opticap^® XLT Capsule
• UNSPSC Code: 23151806

Properties

• Product Name: Opticap^® XLT 10 CapsuleMedia: Millipore Express^® PHF 0.2 µm, Chemistry: Hydrophilic Polyethersulfone (PES)Inlet: 1 in. Hose BarbOutlet: 1 in. Hose BarbT-lineMax Operating Pressure: 80 psi @ 25 °C
• Quality Level: 400
• material: polyethersulfone , polypropylene , polypropylene housing, polypropylene support, polypropylene vent cap, polysulfone , 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 10
• feature: hydrophilic
• manufacturer/tradename: Millipore Express^®
• parameter: ≤30 mL/min air diffusion at 2.8 bar (40 psig) and 23 °C (in water), 1.0 bar max. inlet pressure (15 psi) at 80 °C, 1000 bar max. differential pressure (15 psi) at 80 °C, 2.75 bar max. inlet pressure (40 psi) at 60 °C, 25 °C max. inlet temp., 5.5 bar max. inlet pressure (80 psi) at 25 °C, 5500 mbar max. differential pressure (80 psi) at 25 °C, 80 psig max. inlet pressure
• technique(s): bioburden reduction: suitable
• L: 37.6 cm (14.8 in.)
• W: 7.8 in.
• cartridge nominal length: 10 in. (25 cm)
• diam.: 10.7 cm (4.2 in.)
• filtration area: 0.54 m²
• inlet connection diam.: 1 in.
• inlet to outlet W: 19.8 cm (7.8 in.)
• outlet connection diam.: 1 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^® PHF
• pore size: 0.2 μm
• fitting: 1/4 in. drain/vent hose barb (with double O-ring seal), inlet hose barb, outlet hose barb, (25 mm (1 in.) Hose Barb Inlet and Outlet)

Description

General description

Device Configuration: Capsule

T-line/Gauge Port: T-line

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method
3 autoclave cycles of 60 min @ 126 °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).

Analysis Note

Bacterial Retention
Samples of membrane used in this filter 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 10 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 ≥1 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 wetting instructions of Filters with MILLIPORE EXPRESS^® Membrane user guide
• Storage Statement: Please refer Filters with MILLIPORE EXPRESS^® Membrane user guide
• 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

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

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.