45 results
·
24ms
·
Sources: EU EUDAMED, US FDA
ROSA Spine
FDA 510(k)
FDA Class 2
·Neurology
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·March 13, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·April 10, 2019
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code OLO·February 22, 2019
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code OLO·March 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·April 3, 2019
ProLift Trial
FDA UDI
Life Spine, Inc.·00190837088422·
DISPOSABLE CIRCULAR STAPLER, DISPOSABLE CURVED CUTTER STAPLER, DISPOSABLE LINEAR STAPLERS AND RELOADS, DISPOSABLE HEMORR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MACLIN POWER INTRAVASCULAR ADMINISTRATION SET
FDA 510(k)
FDA Class 2
·General Hospital
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008553·CONTINUOUS / INTERMITTENT SUCTION REGULATOR
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008591·CONTINUOUS / INTERMITTENT SUCTION REGULATOR
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008577·CONTINUOUS / INTERMITTENT SUCTION REGULATOR
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008607·CONTINUOUS / INTERMITTENT SUCTION REGULATOR
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008584·CONTINUOUS / INTERMITTENT SUCTION REGULATOR
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008560·CONTINUOUS / INTERMITTENT SUCTION REGULATOR
CUP: VERSAFITCUP CC TRIO 01.26.45.1156 ACETABULAR SHELL CC TRIO NO-HOLE Ø 56
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·March 16, 2023
FINELINE II
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVN·July 6, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·June 7, 2013