6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HYSTEROSCOPE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ORTHO-J, INC. BEK-JS-004
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PHOENIX DRAPES WITH MICROBAN
FDA 510(k)
FDA Class 1
·General Hospital
BO-HLS 7050 ADVANCED 7.0
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTQ·May 31, 2014
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.
FDA Adverse Event
Malfunction
·COCHLEAR LTD·Product code MCM·November 11, 2010
TOTAL ASR FEM IMP SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·January 4, 2013