7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FIX-L PEEK PLIF and T-PLIF System
FDA 510(k)
FDA Class 2
·Orthopedic
CanMINI Hand and Foot System
FDA 510(k)
FDA Class 2
·Orthopedic
AnyPlus Navigated Instruments System
FDA 510(k)
FDA Class 2
·Neurology
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 9, 2023
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 11, 2014
EPIPEN
FDA Adverse Event
Injury
·DEY PHARMA LP·Product code KZE·September 6, 2011
COULTER® LH 750 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·July 23, 2013