7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
CO2 CUP REAGENT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
UREAPLASMA DIFFERENTIAL BASAL AGAR MED.
FDA 510(k)
FDA Class 1
·Microbiology
LEFORTE NEUROSYSTEM BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
NV GXL LNR, LIPPED, 28MM ID, GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH INC.·Product code LZO·March 22, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2014
CARELINK PROGRAM W/TELEMETRY C
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DXY·October 15, 2012
UNIVERSAL BATTERY CHARGE II
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code MOQ·May 22, 2015