8 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TDX METHOTREXATE
FDA 510(k)
FDA Unclassified
·Unknown
NAIL HOLDING SCREW
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·January 6, 2012
CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221
FDA 510(k)
FDA Class 2
·Cardiovascular
SOFIA(R) RSV FIA
FDA 510(k)
FDA Class 1
·Microbiology
THORATEC® HEARTMATE 3¿ VAD MODULAR CABLE
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·September 13, 2024
OMNIPOD INSULIN PUMP
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·May 13, 2014
GOBED+
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·October 10, 2012
HOT BIOPSY FORCEPS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - COSTA RICA·Product code KGE·September 10, 2010