7 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIOPRO HEMI-ENDO MODULAR CERAMIC HEAD
FDA 510(k)
FDA Class 2
·Orthopedic
Arthrex®
FDA UDI
ARTHREX, INC.·00888867055162·PLATE, POW, LOCKING, TI, 4.5 MM
SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator
FDA 510(k)
FDA Class 2
·Anesthesiology
MODIFICATION TO: MAYFIELD RADIOLUCENT SKULL PINS, MODEL 4-0-A-2020
FDA 510(k)
FDA Class 2
·Neurology
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 9, 2013
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER INC.·Product code MMI·January 7, 2011
PROMUS PREMIER?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 23, 2014