6 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRESSURE CATHETER PLACEMENT SET 50010
FDA 510(k)
FDA Class 2
·Cardiovascular
Kinos Total Ankle System
FDA 510(k)
FDA Class 2
·Orthopedic
KI-20
FDA 510(k)
FDA Class 1
·Dental
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·May 30, 2014
ARTICUL/EZE BALL 32 +1 GR
FDA Adverse Event
Injury
·DEPUY SUZHOU·Product code JDI·November 21, 2012
HEARTSTART MRX - EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·September 16, 2010