MFSL06GT3

Durapore^® 5.0 µm, Millipak^® Final Fill Capsule

Millipak^® Final Fill 60

• Codice UNSPSC: 23151806

Proprietà

• Materiali: polysulfone device; polysulfone support
• Livello qualitativo: 400
• agenzia: meets EP 2.6.14; meets JP 4.01; meets USP 85
• Sterilità: irradiated; non-sterile
• Compatibilità con la sterilizzazione: gamma compatible
• Nome Commerciale: Millipak^® Final Fill 60
• Caratteristiche: hydrophilic
• Produttore/marchio commerciale: Millipak^®
• Parametri: 10 psi max. differential pressure (0.7 bar) at 25 °C (Reverse); 4.5 L/min flow rate at 0.69 bar (ΔP); 5.5 bar max. inlet pressure (80 psi) at 25 °C; 60 L process volume; 80 psi max. differential pressure (5.5 bar) at 25 °C (Forward)
• tecniche: prefiltration: suitable
• Lunghezza: 4.3 in.
• Larghezza: 3.0 in.
• Superficie filtrante del filtro: 300 cm²
• Impurezze: <0.25 EU/mL USP bacterial endotoxins (LAL test, per device; aqueous extraction); <0.25 EU/mL bacterial endotoxins (LAL test, per device; aqueous extraction)
• Matrice: Durapore^®
• Dimensione pori: 5.0 μm pore size
• Punto di bolla: ≥2 psi (138 mbar), air with water
• Raccordi: (38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

Descrizione

Descrizione generale

Device Configuration: Capsule

Confezionamento

Double Easy-Open bag

Nota sulla preparazione

Sterilization Method: Device integrity and retention was maintained after 3 autoclave cycles of 90 minutes at 126  °C. Devices can withstand a dose ≤40  kGy gamma exposure.

This product was manufactured with a Durapore^® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b)(6), validated based on large volume parenteral specifications as detailed in USP 788 Particulate Matter in Injections

Altre note

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 general guidelines section of user guide shipped with this product
• Storage Statement: Please refer user guide shipped with this product
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations

These products are manufactured in a facility which is certified to ISO 9001:2015 Quality Management Systems.

Note legali

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

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