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# FDA Revokes EUAs for B.Braun Covid Devices
- URL: https://www.fdaweb.com/fda-revokes-euas-for-b-braun-covid-devices/
- Published: 2024-12-11T12:00:00.000Z
- Updated: 2026-09-14T14:49:06.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5158345

*Federal Register* notice: FDA is announcing the revocation of a B. Braun Medical emergency use authorizations for its Perfusor Space Syringe Infusion Pump System, Infusomat Space Volumetric Infusion Pump System, and Outlook ES and their use in Covid-19 patients. The company requested the revocation after deciding to discontinue distributing and marketing the devices. To view the notice, click [here](https://public-inspection.federalregister.gov/2024-29247.pdf?ref=fdaweb.com).