24 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Equashield Closed System drug Transfer Device (CSTD)
FDA 510(k)
FDA Class 2
·General Hospital
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486004149·MCK ONLAY INSERT TRIAL (SIZE 6 X 9mm)
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486004156·MCK ONLAY INSERT TRIAL (SIZE 6 X 10mm)
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486004170·MCK ONLAY INSERT TRIAL (SIZE 6 X 12mm)
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486004132·MCK ONLAY INSERT TRIAL (SIZE 6 X 8mm)
TIBIAL INSERT ONLAY TRIAL-SIZE 6-8MM
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code NPJ·March 2, 2018
TIBIAL INSERT ONLAY TRIAL-SIZE 6-8MM
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code NPJ·March 2, 2018
TIBIAL INSERT ONLAY TRIAL-SIZE 6-8MM
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code NPJ·March 2, 2018
TIBIAL INSERT ONLAY TRIAL-SIZE 6-8MM
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code NPJ·March 2, 2018
TIBIAL INSERT ONLAY TRIAL-SIZE 6-8MM
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code NPJ·March 2, 2018
TIBIAL INSERT ONLAY TRIAL-SIZE 6-8MM
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code NPJ·March 2, 2018
TIBIAL INSERT ONLAY TRIAL-SIZE 6-8MM
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code NPJ·March 20, 2018
VENUS BASIC SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EP-WORKMATE
FDA 510(k)
FDA Class 2
·Cardiovascular
TIBIAL INSERT ONLAY TRIAL-SIZE 6-8MM
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code NPJ·March 20, 2018
MYKNEE STD FEMUR DISTAL PIN POSITIONER - MRI - GMK - RIGHT - #6
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·March 14, 2018
MYKNEE STD FEMUR DISTAL PIN POSITIONER - MRI - GMK SPHERE- LEFT - SIZE6+
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·March 14, 2018
ADVISOR VITAL SIGNS MONITOR
FDA Adverse Event
Malfunction
·SMITHS MEDICAL PM, INC.·Product code CCK·December 24, 2008
ADVISOR VITAL SIGNS MONITOR
FDA Adverse Event
Malfunction
·SMITHS MEDICAL PM, INC·Product code DQK·April 28, 2010
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 14, 2013