8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STACKABLE CAGE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CUFF CONNECTOR
FDA 510(k)
FDA Class 1
·Anesthesiology
PROGUIDE CHRONIC DIALYSIS CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INSERT, BIPOLAR FORCEPS
FDA Adverse Event
Malfunction
·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code GEI·April 2, 2015
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 5, 2013
DA+ C SERIES DR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code DXY·February 15, 2011
ADAPTA DR
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code NVZ·August 7, 2014
MENTOR SMOOTH ROUND MODERATE PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·October 23, 2024