7 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DIC TRACHEOSTOMY TUBE AND PORTEX BLUE LINE
FDA 510(k)
FDA Class 2
·Anesthesiology
FLEXIBLE ARTHROSCOPE
FDA 510(k)
FDA Class 2
·Orthopedic
SERIES OF DIAGNOSTIC PHANTOMS
FDA 510(k)
FDA Class 1
·Radiology
SHELL POROUS WITH CLUSTER HOLES
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code LPH·May 26, 2017
NEXGEN CR-FLEX GSF FEMORAL COMPONENT
FDA Adverse Event
Malfunction
·ZIMMER, INC.·Product code JWH·November 23, 2010
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 28, 2013
NATURALYTE
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 27, 2014