KHGES003HH3

Millipore Express^® SHC 0.5/0.2µm, Opticap^® XL 300 Capsule

Fittings 9/16 in. HB/HB, Sterile

• Synonym(e): Opticap Sterile XL 300 Millipore Express SHC 0.5/0.2 μm 9/16 in. HB/HB, Millipore Express^® SHC, Opticap^® XL Capsule
• UNSPSC Code: 23151806
• eCl@ss: 32031690

Eigenschaften

• Produktname: Millipore Express^® SHC, Opticap^® XL Kapsel, Chemistry: Hydrophilic Polyethersulfone (PES)Inlet: 9/16 in. Hose BarbOutlet: 9/16 in. Hose BarbMax Operating Pressure: 80 psi @ 25 °C
• Quality Segment: 400
• material: polyethersulfone membrane, polyethylene support, polypropylene (gamma-stable), polypropylene housing, polypropylene vent cap (Gamma stable), 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^® XL 3
• feature: hydrophilic
• manufacturer/tradename: Millipore Express^®
• parameter: ≤1.9 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 23 °C, 6.9 bar max. differential pressure (100 psid) at 25 °C (Forward; intermittent), 6.9 bar max. inlet pressure (100 psi) at 23 °C (intermittent), 80 psi max. differential pressure (5.5 bar) (continuous), 80 psig max. inlet pressure
• technique(s): sterile filtration: suitable
• L: 11.9 cm (4.7 in.)
• cartridge nominal length: 4.7 in. (11.9 cm)
• diam.: 5.6 cm (2.2 in.)
• filtration area: 290 cm²
• inlet connection diam.: 9/16 in.
• inlet to outlet W: 11.9 cm (4.7 in.)
• outlet connection diam.: 9/16 in.
• impurities: ≤0.25 EU/mL (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 hose barb, outlet hose barb, (14 mm (9/16 in.) Hose Barb Inlet and Outlet)

Beschreibung

General description

Device Configuration: Filtereinheit

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).

Analysis Note

Bacterial Retention
Quantitative Rückhaltung von Brevundimonas diminuta bei einer Mindestbeaufschlagung von 1 x 10⁷ KBE/cm² unter Anwendung der ASTM^® F838-Methode.

Erfüllt die Anforderungen des USP-Tests auf oxidierbare Substanzen nach Durchspülen mit ≥1 l Wasser

TOC/Conductivity
After sterilization and a controlled water flush of 2.0 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.

Other Notes

Diese Produkte werden in einem Werk hergestellt, das den GMP-Richtlinien der FDA entspricht.

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.

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 bestätigt, dass dieses Produkt der europäischen Druckgeräterichtlinie 97/23/EG vom 29. Mai 1997 entspricht. Dieses Produkt wurde unter Artikel 3 § 3 der Druckgeräterichtlinie klassifiziert. Das Produkt wurde in Übereinstimmung mit anerkannten technischen Methoden entwickelt und hergestellt, um einen sicheren Betrieb zu gewährleisten. In Konformität mit Artikel 3 § 3 dieser Druckgeräterichtlinie besitzt dieses Produkt kein CE-Zeichen.