192 results
·
44ms
·
Sources: EU EUDAMED, US FDA
Iradimed Corporation
Manufacturer
🇺🇸 United States·2 Importers
IRADIMED CORPORATION
FDA registration
IRADIMED CORPORATION·5 products·🇺🇸 United States
MRIDIUM 3860+ INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·February 1, 2017
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·October 29, 2012
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·April 23, 2013
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·October 12, 2012
MRIDIUM INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·December 2, 2019
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·February 18, 2014
MRIDIUM INFUSION PUMP
FDA Adverse Event
Death
·IRADIMED CORPORATION·Product code FRN·January 1, 2020
MRIDIUM 3860+ INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·October 29, 2015
MRIDIUM INFUSION SET
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FPA·July 21, 2019
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·September 25, 2012
MRIDIUM 3860+
FDA Adverse Event
Injury
·IRADIMED CORPORATION·Product code FRN·November 27, 2024
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·September 4, 2012
MRIDIUM INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·December 4, 2019
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·September 15, 2014
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·September 25, 2012
3005053560-2018-00001
FDA Adverse Event
Malfunction
·July 26, 2018
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·September 25, 2012
MRIDIUM MRI INFUSION PUMP
FDA Adverse Event
Malfunction
·IRADIMED CORPORATION·Product code FRN·September 25, 2012