29 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IV Fat Emulsion Administration Sets
FDA 510(k)
FDA Class 2
·General Hospital
UNIMED BLOOD PRESSURE CUFF
FDA 510(k)
FDA Class 2
·Cardiovascular
SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY
FDA 510(k)
FDA Class 2
·General Hospital
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
LEKSELL GAMMA KNIFE 4C
FDA Adverse Event
Injury
·ELEKTA INSTRUMENT AB·Product code IWB·June 17, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011
MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·September 23, 2008
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 3, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·June 6, 2018