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Diality Reports the US FDA’s Clearance of its Moda-flx Hemodialysis System

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Diality

Diality Reports the US FDA’s Clearance of its Moda-flx Hemodialysis System

Shots:

  • The US FDA has granted 510(k) clearance to the company’s Moda-flx Hemodialysis System for patients with renal failure
  • The device is developed for acute or chronic renal failure with/without ultrafiltration, in an acute, post-acute, or chronic care facility. Available treatments are Intermittent Hemodialysis (IHD), Sustained Low Efficiency Dialysis (SLED/SLEDD) & Prolonged Intermittent Renal Replacement Therapy (PIRRT)
  • The system features variable flow rates, integrated reverse osmosis water filtration, and an intuitive graphical user interface, enabling customization of hemodialysis based on patient needs
Click here to­ read the full press release 

Disha Nankani

Disha is a content writer at PharmaShots. She is passionate and curious about recent updates and developments in MedTech and Pharma industry. She covers news related to clinical trial results and updates. She can be contacted at connect@pharmashots.com.

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