33 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Y WIRE 2
FDA 510(k)
FDA Class 1
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·00636257128121·20-30 MV FOR MEN SEL EW CLF STD BLK VI
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·00636257129500·20-30 MV FOR MEN CLSC EW STD BLACK VI
HIGH PRESSURE SETS-400 PSI
FDA 510(k)
FDA Class 2
·General Hospital
MICROMESAM BASIC-SET
FDA 510(k)
FDA Class 2
·Anesthesiology
CELSITE ACCESS PORT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL SAS·Product code LJT·May 28, 2014
CELSITE ACCESS PORT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL SAS·Product code LJT·March 21, 2014
CELSITE ACCESS PORT
FDA Adverse Event
Injury
·BBRAUN MEDICAL SAS·Product code LJT·July 1, 2015
CELSITE ACCESS PORT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL SAS·Product code LJT·April 11, 2014
CELSITE
FDA Adverse Event
Injury
·B .BRAUN MEDICAL SAS·Product code LJT·February 20, 2017
CELSITE ACCESS PORT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL SAS·Product code LJT·September 14, 2015
CELSITE
FDA Adverse Event
Injury
·B.BRAUN MEDICAL SAS·Product code LJT·April 8, 2020
CELSITE ACCESS PORT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL SAS·Product code LJT·March 21, 2014
CELSITE
FDA Adverse Event
Injury
·B .BRAUN MEDICAL SAS·Product code LJT·August 3, 2017
CELSITE ACCESS PORT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL SAS·Product code LJT·July 10, 2014
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·May 31, 2013
GEM PREMIER 4000
FDA Adverse Event
Malfunction
·INSTRUMENTATION LABORATORY CO.·Product code CIG·June 16, 2011
RESOLUTION CLIP DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MND·August 28, 2008
CELSITE ACCESS PORT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL SAS·Product code LJT·July 6, 2015
CELSITE ACCESS PORT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL SAS·Product code LJT·December 9, 2014