7 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Mecta-C TiPEEK
FDA 510(k)
FDA Class 2
·Orthopedic
VARIABLE SELF-DRILLING SCREW DIAM. 4X14MM (2X)
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWQ·October 4, 2017
SAPIENS TIP CONFIRMATION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
OPTIV ANTAGE DH POWER INJECTION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 24, 2013
SMARTSETMV MV ENDURANCE 40 G (2 EACH)
FDA Adverse Event
Injury
·DEPUY CMW·Product code LOD·June 23, 2011
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·August 27, 2008