6 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PREFILLED RESPIRATORY THERAPY VIAL
FDA 510(k)
FDA Class 2
·Anesthesiology
AIGIS RX R PM/ AIGIS RX R ICD
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MODIFICATION TO HIOX
FDA 510(k)
FDA Class 2
·Anesthesiology
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·May 23, 2014
NAIL
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·November 14, 2012
ZIMMER M/L MODULAR FEMORAL STEM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWY·September 7, 2010