6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GENESIS POSTERIOR STABILIZED (P/S) KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
WAVE FLUORESCENT MAGNIFIER
FDA 510(k)
FDA Class 1
·General Hospital
FST CATH UD-DUAL DUAL PRESSURE CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HOT SHEARS (TM) MONOPOLARCURVED SCISSORS
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·February 6, 2013
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·January 4, 2011
PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code BTI·July 21, 2014