7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SINGLE USE TUNGSTEN WIRE LEE LOOP ELECTRODE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
U.S. TYPE CRUCIATE SLOT BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
ELECTRODE USING PROMEON RG-60 SERIES GEL
FDA 510(k)
FDA Class 2
·Neurology
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCO·Product code CBK·January 17, 2013
ASKU
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·December 14, 2010
PROMUS PREMIER?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 10, 2014
OXFORD UNI TIB BRG MED SZ4
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·May 14, 2025