421 results · 37ms · Sources: EU EUDAMED, US FDA

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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