33 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OXIMAX PULSE OXIMETRY SYSTEM WITH N-595 PULSE OXIMETER AND OXIMAX SENSORS AND CABLES (AKA ACCESSORIES)
FDA 510(k)
FDA Class 2
·Cardiovascular
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040095201·Maxima K-Files 25mm
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65810128911·K-FILES 31MM #40-70
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131013·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131112·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131037·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130955·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131150·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130979·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130931·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131051·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131136·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131075·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131099·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130993·
MODIFICATION TO HYBRID CAPTURE II CT/GC TEST, MODEL 03M90-01
FDA 510(k)
FDA Class 1
·Microbiology
PANAG
FDA 510(k)
FDA Class 2
·Neurology
ST. JOSEPH HSP BALTIMORE MD1
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DWF·October 1, 2010
AXON ECLIPSE DIGITAL PREAMP
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code GWF·March 1, 2013
FEMORAL NAIL, A/R 10X380 MM
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·March 1, 2011