14 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Access sTfR
FDA 510(k)
FDA Class 2
·Immunology
Oticon
FDA UDI
Sbo Hearing A/S·05714464057627·OTICON PLAY PX 1 MINIRITE T C057
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Injury
·BD·Product code FOZ·August 11, 2015
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Injury
·BD·Product code FOZ·August 11, 2015
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Injury
·BD·Product code FOZ·August 11, 2015
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Injury
·BD·Product code LJS·August 11, 2015
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Injury
·BD·Product code FOZ·August 11, 2015
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Injury
·BD·Product code FOZ·August 11, 2015
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Injury
·BD·Product code FOZ·August 11, 2015
CRYOCHECK CLOT C
FDA 510(k)
FDA Class 2
·Hematology
LTJ Screws and Washer
FDA 510(k)
FDA Class 2
·Orthopedic
WAVELIGHT EX500 EXCIMER LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·November 5, 2014
INSTATRAK 3500
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·August 17, 2011
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FPO·July 17, 2013