EUA

VentMI

FDA Emergency Use Authorization · MakeMedical · Apr 19, 2020

Key facts

Product VentMI
Company MakeMedical
Product type Dual Patient Circuit Connector
Product code QOX
Date Apr 19, 2020
FDA page fda.gov

At a glance

  • 1–9 Authorization documents
  • 1–9 EUAs for this company

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About Emergency Use Authorizations

Emergency Use Authorizations allow the FDA to permit unapproved medical products, or unapproved uses of approved products, during a declared public health emergency.

Source: U.S. Food and Drug Administration (FDA), Emergency Use Authorizations · Source date:

Browse all Emergency Use Authorizations