CGW301SB1

Bevigard^™-P Cartridge Filter

pore size 1.0/0.2 μm, cartridge nominal length 10 in. (25 cm), Code 0 (2-222; O-rings)

• Synonym(e): Bevigard^™-P Cartridge Filter 10 in. 0.2 µm Code 0
• UNSPSC-Code: 23151806
• eCl@ss: 32031610

Eigenschaften

• Materialien: borosilicate glass fiber (BGF) prefilter; mixed cellulose esters (MCE) ; polypropylene ; polypropylene support (Spun bonded); silicone seal
• Einhaltung gesetzlicher Vorschriften: meets EU framework regulation [1935/2004/EC] (all component materials; regarding materials and articles intended to contact food); meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• Hersteller/Markenname: Bevigard^™
• Parameter: 3.5 bar max. differential pressure (50 psid) at 25 °C
• Nennlänge Kartusche: 10 in. (25 cm)
• Durchmesser: 7.1 cm (2.8 in.)
• Filtrationsfläche: 0.46 m²
• Verunreinigungen: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
• Gravimetrisch bestimmte extrahierbare Substanzen: ≤140 mg/cartridge
• Matrix: Bevigard^™-P
• pore size: 1.0/0.2 μm pore size
• Aufnahme: sample type liquid; sample type bottled water; sample type beer; sample type beverage(s); sample type food(s); sample type wine
• Kartuschencode: Code 0 (2-222; O-rings)

Beschreibung

Allgemeine Beschreibung

Device Configuration: Filterelement

Leistungsmerkmale und Vorteile

Format: Double Layer

Verpackung

Leicht zu öffnender Doppelbeutel

Sonstige Hinweise

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 to installation and wetting sections of OptiScale^®-25 user guide and introduction section of Mixed celulose esters Tech Brief
• Storage Statement: Please refer Mixed cellulose esters Tech Brief
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Angaben zur Herstellung

Sanitization Protocol
30 min mit 80 °C heißem Wasser

Sterilization Method
10 Autoklaven- oder In-situ-Dampfsterilisationszyklen von 30 min bei 121 °C

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).

Hinweis zur Analyse

Erfüllt die Anforderungen des USP-Tests auf oxidierbare Substanzen nach Durchspülen mit ≥5 l Wasser

Gravimetric Extractables: after 24 hours in water at controlled room temperature

Rechtliche Hinweise

Bevigard is a trademark of Merck KGaA, Darmstadt, Germany

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

Sicherheitshinweise

• Piktogramme: GHS02,GHS08
• Signalwort: Danger
• H-Sätze: H228,H350i
• P-Sätze: P202 - P210 - P240 - P241 - P280 - P308 + P313
• Gefahreneinstufungen: Carc. 1B Inhalation - Flam. Sol. 1
• Lagerklassenschlüssel: 4.1B - Flammable solid hazardous materials
• WGK: WGK 3