6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WELLCOGEN S. PNEUMONIAE
FDA 510(k)
FDA Class 1
·Microbiology
INERTIA PEDICLE SCREW SYSTEM, HONOUR SPACER SYSTEM, FACET FIXX, STRUXXURE ANTERIOR CERVICAL PLATE AND SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054; OPTIONAL PRINTER FOR CI, MODEL M3925A
FDA 510(k)
FDA Class 2
·Cardiovascular
HAKIM PROGRAMMABLE VALVE WITHOUT PRECHAMBER
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code JXG·May 30, 2014
UNKNOWN DEPUY ASR FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·November 21, 2012
COLLEAGUE CXE VOLUMETRICINFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 22, 2010