Feb 16, 2021

Medtronic Statement - Per FDA Guidance, Medtronic Temporarily Modifies Critical Care Products to Address COVID-19

Temporary Limited Modifications to Bio-Medicus Adult Cannulae and Introducers, Bio-Medicus Cannulae Kits, & Bio-Medicus Pediatric Cannulae and Introducers Indications to Support Longer Duration Use in ECMO Therapy to Address COVID-19

DUBLIN, February 16, 2021 ― During this critical time, Medtronic remains committed to our strategy of delivering critical care products ― designed and indicated for Extracorporeal Membrane Oxygenation (ECMO) ― to treat patients around the world. Following guidance issued by the U.S. Food and Drug Administration (FDA) on April 6, 2020, certain FDA-cleared Bio-Medicus Cannulae are now permitted to temporarily be used in the U.S. for ECMO therapy greater than six hours.

Under this new guidance the FDA is allowing temporary limited modifications to the indications of certain FDA-cleared or FDA-approved cardiopulmonary devices without prior submission of premarket notification. These modifications are allowed, considering the public health emergency, when they do not create an undue risk. This limited indication modification for ECMO therapy greater than six hours has not been cleared or approved by the FDA and is in effect only for the duration of the public health emergency related to COVID-19 as declared by the Department of Health and Human Services (HHS).

The devices listed below are currently FDA-cleared for extracorporeal support for periods appropriate to cardiopulmonary bypass procedures (up to 6 hours).

In accordance with the new FDA guidance, the devices listed below can now be used for longer than 6 hours in an ECMO circuit to treat patients who are experiencing acute respiratory/cardiopulmonary failure during the COVID-19 Public Health Emergency.

Bio-Medicus Cannulae

Model

Description

96820-108

96820-110

96820-112

96820-114

96830-108

96830-110

96830-112

96830-114

Bio-Medicus™ Pediatric Femoral Cannulae and Introducers

96570-115

96570-117

96570-119

96570-121

96570-123

96570-125

96670-127

96670-129

Bio-Medicus™ Adult Femoral Arterial/Jugular Venous Cannulae and Introducers

96670-115

96670-117

96670-119

96670-121

96670-123

96670-125

Bio-Medicus™ Adult Femoral Venous Cannulae and Introducers

96530-115

96530-117

96530-119

96530-121

96530-123

96530-125

96600-127

96600-129

Bio-Medicus™ Adult Femoral Arterial/Jugular Venous Cannulae Kit

96600-115

96600-117

96600-119

96600-121

96600-123

96600-125

Bio-Medicus™ Adult Femoral Venous Cannulae Kit

 

The special supplement to the products’ Instructions for Use (IFU) can be found on the Medtronic website for U.S. eManuals. This special supplement contains information on:

  • Available data on design characteristics and use conditions related to ECMO
  • Performance and durability testing summary
  • Potential risks related to the use of the device for ECO
  • Clinical signs or observations that require device change-out

Extracorporeal membrane oxygenation (ECMO) is a life supporting therapy. People who need ECMO have a severe and life-threatening illness that stops their heart or lungs from working properly. ECMO therapy temporarily replaces the function of the heart and/or lungs by pumping blood from the patient’s body to an oxygenator that provides long term physiological gas exchange (oxygen and carbon-dioxide transfer).