6 results
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24ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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BARD® URETHRAL CATHETERIZATION TRAY WITH RED RUBBER CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·May 9, 2022
BARD® URETHRAL CATHETERIZATION TRAY WITH VINYL CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·May 9, 2022
BARD® URETHRAL CATHETERIZATION TRAY WITH VINYL CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·October 31, 2018
*
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·August 28, 2012
ACRYSOF
FDA Adverse Event
Malfunction
·ALCON MANUFACTURING, LTD.·Product code HQL·December 18, 2013
LCP PROX-FEMPL 4.5/5 LE SHAFT 4HO L175 S
FDA Adverse Event
Malfunction
·SYNTHES ELMIRA·Product code HRS·June 25, 2013