Business · 12/12/2024Updated: 10/17/2026 · 1 min read
FDA Revokes Emergency Use Authorization for B. Braun Medical's Infusion Pump Systems
Summary
The FDA has revoked the Emergency Use Authorization for B. Braun Medical's Perfusor Space Syringe Infusion Pump System, Infusomat Space Volumetric Infusion Pump System, and Outlook ES, following a request from the company itself.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →