11 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DISPOSABLE BITE BLOCK/TONGUE DEPRESSOR
FDA 510(k)
FDA Class 2
·Neurology
LEONE SPA
FDA UDI
LEONE SPA·08033707079996·WEB 1ST MOLAR BANDS UL KIT
H2 HEATED HUMIDIFIER
FDA 510(k)
FDA Class 2
·Anesthesiology
STA COMPACT MAX
FDA 510(k)
FDA Class 2
·Hematology
CENTRA BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·May 8, 2014
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 13, 2012
OUTBACK RE-ENTRY CATHETER
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code DQY·September 10, 2010
SM HYBRID GLENOID BASE 4MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·December 7, 2020
VERSA-DIAL/COMP TI STD TAPER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·December 7, 2020
VERSA-DIAL 38X19X39 HUM HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·December 7, 2020
PT HYBRID GLEN POST REGENEREX
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·December 7, 2020