10 psi max. differential pressure (0.7 bar) at 25 °C (Reverse) 200 L process volume 5.5 bar max. inlet pressure (80 psi) at 25 °C 7.61 L/min flow rate at 1.1 bar (ΔP) 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
分析说明
Bacterial Grow-Through: Quantitative retention of 1 x 107 CFU/cm2Brevundimonas diminuta ATCC® 19146 per ASTM® F838 methodology.
其他说明
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.
法律信息
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