33 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Cellvizio 100 Series System with Confocal Miniprobes
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
B-P TOTAL HIP SYSTEM
FDA UDI
ENDOTEC, INC.·00814193023346·B-P HIP SELF-ALIGNING ACETABULAR CUP & BEARING ...
SYNOVO HIP COMPONENTS
FDA UDI
Synovo Production·00814193026026·HIP SELF-ALIGNING ACETABULAR CUP & BEARING - 28...
REHASTIM 2, REHAMOVE 2
FDA 510(k)
FDA Class 2
·Neurology
ALL-BOUND 3
FDA 510(k)
FDA Class 2
·Dental
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·October 17, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 9, 2018
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·January 11, 2019
PUSHING CATHETER
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 19, 2022
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 21, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·December 21, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
CRYSTALENS INTRAOCULAR LENS
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code NAA·October 9, 2014
DPM 6 / MPM MODULE
FDA Adverse Event
Malfunction
·MINDRAY DS USA, INC·Product code MHX·May 21, 2013
HEM-O-LOK ENDO 5
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code GDO·September 17, 2008
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018