6 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PROFORM POROUS BEADED FEMORAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
BIOMAGNETIC TECHNOLOGIES NEUROMAGNEOMETER
FDA 510(k)
FDA Class 2
·Neurology
MODEL #250 DEFIB CABLE
FDA 510(k)
FDA Class 2
·Cardiovascular
SIGMA 100 S
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NVZ·February 11, 2013
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTL., LTD.·Product code KWA·January 5, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 24, 2014