KGW9A2TTT1

Polysep^™ II 2.0/1.2 µm nominal, Opticap^® XLT Capsule

inlet connection diam. 1.5 in., Opticap^® XLT 20, pore size 2.0/1.2 μm, cartridge nominal length 20 in. (50 cm)

• Sinónimos: Opticap XLT20 Polysep II 2.0/1.2 μm 1-1/2 in. TC
• Código UNSPSC: 23151806
• eCl@ss: 32031610

Propiedades

• Materiales: borosilicate glass fiber (BGF) membrane; mixed cellulose esters (MCE) membrane; polypropylene ; polypropylene housing; polypropylene support; polypropylene vent cap; silicone seal
• Nivel de calidad: 400
• cumplimiento norm.: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• esterilidad: non-sterile
• Compatibilidad de esterilización: autoclavable compatible
• Línea del producto: Opticap^® XLT 20
• Características: hydrophilic
• fabricante / nombre comercial: Opticap^®
• Parámetros: 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
• técnicas: prefiltration: suitable
• Longitud: 62.5 cm (24.6 in.)
• Anchura: 6.0 in.
• longitud nominal del cartucho: 20 in. (50 cm)
• filtración área: 0.93 m²
• diám. conexión a entrada: 1.5 in.
• An entrada a salida: 15.2 cm (6.0 in.)
• diám. conexión a salida: 1.5 in.
• impurezas: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• extraíbles gravimétricos: ≤290 mg/capsule
• matriz: Polysep^™ II
• pore size: 2.0/1.2 μm nominal pore size; 2.0/1.2 μm pore size
• entrada: sample type liquid
• Adaptador: inlet sanitary flange; outlet sanitary flange; (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

Descripción

Descripción general

Device Configuration: Capsule

T-line/Gauge Port: T-line

Características y beneficios

Format: Double Layer

Envase

Double Easy-Open bag

Otras notas

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

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 to the first page of Visual Inspection Guide and introduction section of the Mixed cellulose esters Tech Brief
• Storage Statement: Please refer to the Mixed cellulose esters Tech Brief
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Nota de preparación

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).

Nota de análisis

Gravimetric Extractables: after a 10 L flush and 24 hours in water at controlled room temperature

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥10 L

Información legal

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

Polysep is a trademark of Sigma-Aldrich Co. LLC

Cláusula de descargo de responsabilidad

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.

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 2