421 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TYSHAK
FDA Adverse Event
Other
·B. BRAUN MEDICAL INC.·Product code MAD·November 10, 2006
NA
FDA Adverse Event
Death
·B. BRAUN MEDICAL, INC.·Product code DXF·December 27, 2006
PALMAZ XL STENT PER 40MM UNMOUNTED
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code FGE·July 1, 2013
TYSHAK II
FDA Adverse Event
Other
·B. BRAUN MEDICAL, INC.·Product code DQY·November 16, 2006
TYSHAK II CATHETER
FDA Adverse Event
Malfunction
·NUMED CANADA, INC.·Product code DQY·April 15, 2019
COVERED C-P STENT
FDA Adverse Event
Injury
·NUMED, INC·Product code PNF·August 12, 2023
Z-MED II
FDA Adverse Event
Other
·B. BRAUN MEDICAL INC.·Product code LIT·December 12, 2006
TYSHAK II
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code DQY·October 5, 2015
BIB CATHETER
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code NVM·August 7, 2018
Z-MED II
FDA Adverse Event
Other
·B. BRAUN MEDICAL INC.·Product code LIT·September 11, 2006
NUCLEUS AORTIC 20 MM
FDA Adverse Event
Injury
·NUMED, INC.·Product code OZT·August 12, 2023
TYSHAK II CATHETER
FDA Adverse Event
Malfunction
·NUMED CANADA, INC.·Product code LIT·July 20, 2020
COVERED CP STENT
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code PNF·December 15, 2016
COVERED CP STENT
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code PNF·December 15, 2016
TYSHAK II
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code DQY·October 6, 2016
IMPACT CATHETER
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code LIT·January 19, 2012
TYSHAK II CATHETER
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code LIT·March 12, 2012
TYSHAK-X CATHETER
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code LIT·January 19, 2012
NUCLEUS-X
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code OZT·April 1, 2014
TYSHAK
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code DQY·April 10, 2014