1.5 L/min flow rate at 0.69 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)
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
其他說明
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.
法律資訊
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIPAK is a registered trademark of Merck KGaA, Darmstadt, Germany