6 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
EDGE ORTHOPAEDICS BITE COMPRESSION SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
SHELHIGH NO-REACT BIOCUFF
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BIOMET MOM HIP
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·November 6, 2014
ION¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·September 2, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 18, 2013