7 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GUILLOTINE BLADE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
CANTATA(R) 2.9 MICROCATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
TI FENESTRATED PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
CANTATA 2.9 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·September 14, 2017
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 27, 2014
DEXTRUS SEAL CAP ASSEMBLY
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GCJ·November 30, 2007
ALIGN TO URETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·BARD SHANNON LIMITED·Product code FTL·November 9, 2012