39 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)
FDA 510(k)
FDA Class 2
·Orthopedic
SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS
FDA UDI
HF ACQUISITION CO. LLC·00850065007489·
MODIFICATION TO: WINNER ST-2 STIMULATOR
FDA 510(k)
FDA Class 2
·Physical Medicine
BIRD TBIRD LEGACY VENTILATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
NONE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·September 3, 2008
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 4, 2019
SYNCHRO 14 NEURO GUIDEWIRE
FDA Adverse Event
Injury
·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 24, 2007
SYRINGE CONTROL 10ML LL BNS
FDA Adverse Event
Injury
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 5, 2019
10 ML BD LUER-LOK CONTROL SYRINGE
FDA Adverse Event
Injury
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 5, 2019
SYNCHRO -10 NEURO GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQX·December 15, 2006
SYNCHRO-14 NEURO GUIDEWIRE
FDA Adverse Event
Malfunction
·NEUROVASCULAR , A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQX·December 19, 2006
SYNCHRO 14 GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007
SYNCHRO .014 GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP. / NEUROCASCULAR DIVISION·Product code DQX·August 16, 2007
SYNCHRO .014 GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP. / NEUROVASCULAR DIV.·Product code DQX·August 16, 2007
SYNCHRO -14 NEURO GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIVISION·Product code DQX·November 30, 2006
SYNCHRO-14 NEURO GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQX·September 12, 2007
SYNCHRO GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code DQX·October 16, 2009
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, LTD (HAIFA, ISRAEL)·Product code DQK·March 27, 2013
TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 18, 2011
ACRYSOF
FDA Adverse Event
Other
·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·March 21, 2008