7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SARGON CYLINDRO-BLADE IMPLANT
FDA 510(k)
FDA Class 2
·Dental
Barco
FDA UDI
FIMI SRL·05415334003118·MDRC-2324 HTEW
SERVO GUARD, MODEL 64 81 290 EH88E
FDA 510(k)
FDA Class 2
·Anesthesiology
Femur Reconstruction Interlocking Nail System, Femur Retrograde Interlocking Nail System, Humerus Interlocking Nail System, Tibia Interlocking Nail System, Compression Hip Nail System
FDA 510(k)
FDA Class 2
·Orthopedic
ESPRIT
FDA Adverse Event
Malfunction
·SORIN BIOMEDICA C.R.M., S.R.L.·Product code NVZ·November 18, 2010
OT VERIO IQ METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 25, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 11, 2014