CHVE72HS3

Millipore Express^® SHR High Area with prefilter 0.5/0.1µm Cartridge 20

Code 0 Silicone, Autoclavable and SIP

• Synonym(s): Millipore Express^® SHRP High Area, Cartridge
• UNSPSC Code: 23151806

Properties

• Product Name: Millipore Express^® SHR w/Prefilter High Area Cartridge, Chemistry: 0.5 / 0.1 µm Hydrophilic Polyethersulfone (PES) Configuration: 20 in. Code 7
• material: polypropylene support, silicone seal
• reg. compliance: meets FDA 21 CFR 177-182 (all component materials)
• manufacturer/tradename: Millipore Express^®
• parameter: ≤108.4 mL/min air diffusion at 3.45 bar (50 psig) (in water), 1700 mbar max. differential pressure (25 psi) at 80 °C (Forward), 1700 mbar max. inlet pressure (25 psi) at 80 °C (Forward), 2100 mbar max. inlet pressure (30 psi) at 25 °C (Reverse), 340 mbar max. differential pressure (5 psi) at 135 °C (Forward), 340 mbar max. inlet pressure (5 psi) at 135 °C (Forward), 69 mbar max. inlet pressure (1 psi) at 135 °C (Reverse), 6900 mbar max. differential pressure (100 psi) at 25 °C (Forward), 6900 mbar max. inlet pressure (100 psi) at 25 °C (Forward)
• Quality Level: 400
• L: 20 in.
• W: 2.8 in.
• cartridge nominal length: 20 in. (50 cm)
• filter diam.: 2.7 in. (6.9 cm)
• filter filtration area: 2.0 m²
• filter size: 20 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^® SHR (w/Prefilter High Area)
• pore size: 0.5/0.1 μm pore size
• bubble point: ≥2586 mbar (37.5 psig), nitrogen with 70/30% IPA/water
• cartridge code: Code 7
• sterility: non-sterile
• sterilization compatibility: autoclavable compatible; steam-in-place compatible
• product line: Millipore Express^®
• feature: hydrophilic, with prefilter

Description

General description

Cartridge Type: Liquid

Device Configuration: Cartridge

Packaging

Double Easy-Open bag

Preparation Note

Sterilization Method: 5 autoclave cycles of 60 min at 126 °C or 5 forward SIP cycles of 30 min at 135 °C

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

After sterilization and a controlled water flush of 40 L, samples exhibited <500 ppb TOC per USP 643 and <1.3 μS/cm per USP 645 at 25 °C.

Bacterial Retention: Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM^® F838 methodology.

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