7 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RESPOSABLE OMNI TIP(TM) SWITCHABLE TIPS (MULTIPLE)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
POST MYDRIATIC SPECTACLES
FDA 510(k)
FDA Class 1
·Ophthalmic
ACS HI-TORQUE FLOPPY GUIDE WIRE, 0.018 INCH
FDA 510(k)
FDA Class 2
·Cardiovascular
UNKNOWN PRODUCT - SET SCREW
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012
CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·February 15, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 29, 2014
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011