8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Klassic Knee System - Revision Tibial Baseplate
FDA 510(k)
FDA Class 2
·Orthopedic
2.5MM DRILL BIT/QC/GOLD/110MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HWE·August 12, 2016
CanGaroo RM Antibacterial Envelope
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Enbio S
FDA 510(k)
FDA Class 2
·General Hospital
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 9, 2023
530G INSULIN PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·November 11, 2014
POWER PORT CATHETER
FDA Adverse Event
Other
·BARD·Product code LJT·September 7, 2011
SCREWDRIVER AXSOS T15 4.0MM LOCKING SET
FDA Adverse Event
Malfunction
·STRYKER TRAUMA SELZACH·Product code LXH·July 24, 2013