CPGE71TP

Millipore Express^® PHF, Cartridge

pore size 0.2 μm, cartridge nominal length 10 in. (25 cm), Code 7, silicone seal

• Synonim(y): Millipore Express^® PHF Cartridge Filter 10 in. 0.2 µm Code 7 Silicone
• Kod UNSPSC: 23151806
• eCl@ss: 32031690

Właściwości

• Materiały: polyethersulfone ; polypropylene ; polypropylene support; polysulfone ; silicone seal
• Poziom jakości: 400
• zgodność regionalna: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• sterylność: non-sterile
• Kompatybilność ze sterylizacją: autoclavable compatible; steam-in-place compatible
• linia produktu: Millipore Express^®
• Właściwości: hydrophilic
• producent / nazwa handlowa: Millipore Express^®
• Parametry: ≤30 mL/min air diffusion at 2.76 bar (40 psig) and 23 °C (in water); 0.07 bar max. differential pressure (1 psid) at 135 °C (Reverse); 0.35 bar max. differential pressure (5 psid) at 135 °C (Forward); 1.0 psi max. differential pressure (69 mbar) at 135 °C (Reverse); 1.4 bar max. differential pressure (20 psid) at 25 °C (Reverse); 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward); 20 psi max. differential pressure (1.4 bar) at 25 °C (Reverse); 25 psi max. differential pressure (1.7 bar) at 80 °C (Forward); 5.0 psi max. differential pressure (340 mbar) at 135 °C (Forward); 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward); 80 psi max. differential pressure (5.5 bar) at 25 °C (Forward)
• metody: bioburden reduction: suitable
• Długość: 10 in.
• Szerokość: 2.7 in.
• długość nominalna kartridża: 10 in. (25 cm)
• Średnica: 6.9 cm (2.7 in.)
• powierzchnia filtracyjna: 0.54 m²
• zanieczyszczenia: ≤0.25 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• Matryca: Millipore Express^® PHF
• wielkość porów: 0.2 μm pore size
• moc wejściowa: sample type liquid
• kod wkładu: Code 7

Opis

Opis ogólny

Device Configuration: Cartridge

Opakowanie

Double Easy-Open bag

Inne uwagi

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 wetting instructions of Filters with MILLIPORE EXPRESS^® Membrane user guide
• Storage Statement: Please refer Filters with MILLIPORE EXPRESS^® Membrane user guide
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Uwaga dotycząca przygotowania

Sterilization Method
12 forward or 22 forward and 3 reverse SIP cycles of 30 min @ 135 °C; 15 autoclave cycles of 60 min @ 126 °C

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).

Komentarz do analizy

Bacterial Retention
Samples of membrane used in this filter were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM^® F838 methodology.

TOC/Conductivity
After sterilization and a controlled water flush of 10 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L

Informacje prawne

ASTM is a registered trademark of American Society for Testing and Materials

MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany

Ta strona może zawierać tekst przetłumaczony maszynowo.