706 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Phasix ST Mesh with Echo 2 Positioning System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OsteoMed
FDA UDI
OSTEOMED LLC·00842528127377·2.0 X 8mm Cannulated Headed Screw, T7
OsteoMed
FDA UDI
OSTEOMED LLC·00845694005470·165mm x 95mm Pre-Formed Osteoform Mesh, Extra-R...
BIONET BM3PLUS PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
GLIDESHEATH
FDA 510(k)
FDA Class 2
·Cardiovascular
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818545·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818538·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818569·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818576·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818552·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818583·
ACRYSOF TORIC
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./ HUNTINGTON·Product code MJP·September 17, 2008
ACRYSOF TORIC
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./ HUNTINGTON·Product code MJP·September 17, 2008
N600 PULSE OXIMETER
FDA Adverse Event
Malfunction
·COVIDIEN/ FORMERLY TYCOHEALTHCARE·Product code DQA·April 25, 2008
ABACUS V2.0 TPN CALCULATING SOFTWARE
FDA Adverse Event
Other
·BAXA CORP.·Product code LNX·December 18, 2008
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES·Product code MIH·June 19, 2008
ACRYSOF
FDA Adverse Event
Other
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·July 18, 2008
ACRYSOF TORIC
FDA Adverse Event
Other
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·July 18, 2008
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON MANUFACTURING, LTD./ HUNTINGTON·Product code MFK·February 6, 2008
ACRSYOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD.·Product code HQL·May 16, 2008