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MFGB06ST3

Millipore

Hydrophobic Durapore® 0.22 µm, Millipak® Final Fill Capsule

Millipak® Final Fill 60, sterile; γ-irradiated

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Codice UNSPSC:
23151806

Materiali

polysulfone device
polysulfone support

Livello qualitativo

agenzia

meets EP 2.6.14
meets JP 4.01
meets USP 85

Sterilità

irradiated
sterile; γ-irradiated

Nome Commerciale

Millipak® Final Fill 60

Caratteristiche

hydrophilic

Produttore/marchio commerciale

Millipak®

Parametri

1.51 L/min flow rate at 0.86 bar (ΔP)
10 psi max. differential pressure (0.7 bar) at 25 °C (Reverse)
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

sterile filtration: suitable

filter filtration area

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

0.22 μm pore size

Raccordi

(38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

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Descrizione generale

Device Configuration: Gamma Gold 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

Risultati analitici

Bacterial Grow-Through: Quantitative retention of 1 x 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per 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 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

ASTM is a registered trademark of American Society for Testing and Materials
ATCC is a registered trademark of American Type Culture Collection
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPAK is a registered trademark of Merck KGaA, Darmstadt, Germany

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