9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UNIVERSAL-ERGOTEST
FDA 510(k)
FDA Class 2
·Physical Medicine
BAC-T-SCREEN BACTERIURIA DETECTION DEV
FDA 510(k)
FDA Class 1
·Microbiology
T4 RIA
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LIFEVEST WCD 3100 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORP·Product code MVK·October 26, 2012
TOTAL HIP BALL 28MM +5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·June 2, 2014
OMNIPOD INSULIN PUMP
FDA Adverse Event
Other
·INSULET CORPORATION·Product code LZG·September 21, 2010
PIPELINE
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 18, 2019
PIPELINE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 18, 2019
PIPELINE
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 18, 2019