7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TENDERFOOT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DIATEMP ELECTROSURGICAL PEN
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
10B
FDA 510(k)
FDA Class 1
·Microbiology
LONG NAIL KIT R2.0, TI, RIGHT GAMMA3 11X360MM X 1
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code JDS·October 11, 2012
BRAVO
FDA Adverse Event
Malfunction
·GIVEN IMAGING LTD.·Product code FFT·October 21, 2010
INFUSOMAT SPACE PUMP SETS WITH CARESITE
FDA Adverse Event
Malfunction
·B. BRAUN DOMINICAN REPUBLIC·Product code FRN·February 14, 2014
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·December 21, 2012