6 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TENS AND EMS (TENS and Muscle Stimulator) ( Model AS8012C,AS8016,AS8019,AS9020E,AS9026)
FDA 510(k)
FDA Class 2
·Neurology
NuEra Tight RF Family
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Identity Shoulder System
FDA 510(k)
FDA Class 2
·Orthopedic
EGIA 60 ARTICULATING MED/THICK SULU
FDA Adverse Event
Injury
·UNITED STATES SURGICAL·Product code GDW·September 7, 2011
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·November 11, 2014
RESERVOIR 3ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·July 23, 2013