6 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
WASHERLOC SCREW SYSTEM, LIGAMENT SCREW SYSTEM, NO-PROFILE BI-CORTICAL SCREW SYSTEM, CHANNEL LIGAMENT CLAMP, HECKMAN SCRE
FDA 510(k)
FDA Class 2
·Orthopedic
Disposable Temperature Probe
FDA 510(k)
FDA Class 2
·General Hospital
HEMODIALYSIS CONCENTRATE, SODIU
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 28, 2013
CAROTID WALLSTENT MONORAIL ENDOPROSTHESIS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIM·February 8, 2011
ACCU-CHEK ® PERFORMA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·August 5, 2014