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CVEP01TS3

Millipore

Millipore Express® SHR, Cartridge

cartridge nominal length 10 in. (25 cm), filter diam. 2.7 in. (6.9 cm)

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About This Item

Codice UNSPSC:
23151806

Materiali

polypropylene support
silicone seal

Conformità normativa

meets FDA 21 CFR 177-182 (all component materials)

Sterilità

non-sterile

Compatibilità con la sterilizzazione

autoclavable compatible
steam-in-place compatible

Nome Commerciale

Millipore Express®

Caratteristiche

hydrophilic

Produttore/marchio commerciale

Millipore Express®

Parametri

≤33.3 mL/min air diffusion at 3.45 bar (50 psig) (in water)
0.35 bar max. differential pressure (5 psi) at 135 °C (Forward)
1.7 bar max. differential pressure (25 psi) at 80 °C (Forward)
1700 mbar max. differential pressure (25 psi) at 80 °C (Forward)
2.1 bar max. differential pressure (30 psi) at 25 °C (Reverse; intermittent)
2100 mbar max. differential pressure (30 psi) at 25 °C (Reverse)
340 mbar max. differential pressure (5 psi) at 135 °C (Forward)
6.9 bar max. differential pressure (100 psi) at 25 °C (Forward)
69 mbar max. differential pressure (<1.0 psi) at 135 °C (Reverse)
6900 mbar max. differential pressure (100 psi) at 25 °C (Forward)

tecniche

sterile filtration: suitable

Lunghezza

10 in.

Larghezza

2.7 in.

Lunghezza nominale della cartuccia

10 in. (25 cm)

Diam. filtro

2.7 in. (6.9 cm)

filter filtration area

0.6 m2

Dimens. filtro

10 in.

Impurezze

≤0.25 EU/mL bacterial endotoxins (LAL test, aqueous extraction)
<0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

Matrice

Millipore Express® SHR

Dimensione pori

0.1 μm

Punto di bolla

≥2586 mbar (37.5 psig), nitrogen with 70/30% IPA/water

Codice cartuccia

Code 0

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Descrizione generale

Cartridge Type: Liquid
Device Configuration: Cartridge

Confezionamento

Double Easy-Open bag

Nota sulla preparazione

Sterilization Method: 25 forward or 22 forward and 3 reverse SIP cycles of 30 min at 135 °C; 25 autoclave cycles of 60 min at 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).

Risultati analitici

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

TOC/Conductivity: After sterilization and a controlled water flush of 10 L, samples exhibited <500 ppb TOC per USP 643 and <1.3 μS/cm per USP 645 at 25 °C.

Bacterial Retention: Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 107 CFU/cm2 using ASTM® F838 methodology.

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 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

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

Note legali

ASTM is a registered trademark of American Society for Testing and Materials
MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany

Certificati d'analisi (COA)

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