8 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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iFuse Bedrock Granite® Implant System
FDA 510(k)
FDA Class 2
·Orthopedic
Vu a-POD™
FDA UDI
Seaspine Orthopedics Corporation·10889981041861·35x27mm Trial Rasp 8mm 8 deg
PLUS PIVOT LINK UNIVERSAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
RESOLUTIONMD MOBILE
FDA 510(k)
FDA Class 2
·Radiology
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·September 27, 2023
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·September 2, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·November 6, 2014
TOTAL ASR ACET IMP SIZE 54
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·July 18, 2013