KGW2A3TTT1

Polysep^™ II 1.0/1.2 µm nominal, Opticap^® XLT Capsule

inlet connection diam. 1.5 in., Opticap^® XLT 30, pore size 1.2/1.0 μm, cartridge nominal length 30 in. (75 cm)

• Sinonimo/i: Opticap XLT30 Polysep II 1.0/1.2 μm 1-1/2 in. TC
• Codice UNSPSC: 23151806
• eCl@ss: 32031610

Proprietà

• Materiali: borosilicate glass fiber (BGF) membrane; mixed cellulose esters (MCE) membrane; polypropylene ; polypropylene housing; polypropylene support; polypropylene vent cap; silicone seal
• Livello qualitativo: 400
• Conformità normativa: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• Sterilità: non-sterile
• Compatibilità con la sterilizzazione: autoclavable compatible
• Nome Commerciale: Opticap^® XLT 30
• Caratteristiche: hydrophilic
• Produttore/marchio commerciale: Opticap^®
• Parametri: 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
• tecniche: prefiltration: suitable
• Lunghezza: 87.1 cm (34.3 in.)
• Lunghezza nominale della cartuccia: 30 in. (75 cm)
• Superficie filtrante: 1.38 m²
• Diam. connessione ingresso: 1.5 in.
• Amp. ingresso/ uscita: 15.2 cm (6.0 in.)
• Diam. connessione uscita: 1.5 in.
• Impurezze: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• Estraibili (gravimetria): ≤435 mg/capsule
• Matrice: Polysep^™ II
• pore size: 1.0/1.2 μm nominal pore size; 1.2/1.0 μm pore size
• input: sample type liquid
• Raccordi: inlet sanitary flange; outlet sanitary flange; (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

Descrizione

Descrizione generale

Device Configuration: Capsule

T-line/Gauge Port: T-line

Caratteristiche e vantaggi

Format: Double Layer

Confezionamento

Double Easy-Open bag

Altre note

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 sulla preparazione

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).

Risultati analitici

Gravimetric Extractables: after a 15 L flush and 24 hours in water at controlled room temperature

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥15 L

Note legali

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

Polysep is a trademark of Sigma-Aldrich Co. LLC

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 11 - Combustible Solids
• Classe di pericolosità dell'acqua (WGK): WGK 2